- Open Access
Mechanistic understanding of nanoparticles’ interactions with extracellular matrix: the cell and immune system
Particle and Fibre Toxicology volume 14, Article number: 22 (2017)
Extracellular matrix (ECM) is an extraordinarily complex and unique meshwork composed of structural proteins and glycosaminoglycans. The ECM provides essential physical scaffolding for the cellular constituents, as well as contributes to crucial biochemical signaling. Importantly, ECM is an indispensable part of all biological barriers and substantially modulates the interchange of the nanotechnology products through these barriers. The interactions of the ECM with nanoparticles (NPs) depend on the morphological characteristics of intercellular matrix and on the physical characteristics of the NPs and may be either deleterious or beneficial. Importantly, an altered expression of ECM molecules ultimately affects all biological processes including inflammation. This review critically discusses the specific behavior of NPs that are within the ECM domain, and passing through the biological barriers. Furthermore, regenerative and toxicological aspects of nanomaterials are debated in terms of the immune cells-NPs interactions.
Extracellular matrix (ECM) represents a complex network of variously modified proteins and the glycosaminoglycan, hyaluronan, highly organized in a form of a suprastructure which ultimately constitutes the cell microenvironment . The ECM proteins are usually classified into two main categories: fibrous proteins constituted of various collagens and elastin, and glycoproteins including fibronectin, glycosaminoglycan decorated protein-proteoglycans and laminin  (Fig. 1). Cells are embedded in hydrogels comprising these different biopolymers and proteoglycans that fill the extracellular space . Moreover, the ECM architecture is highly specialized and tightly regulated as the result of inherent properties of the component molecules, as well as of the biologic potency of the dwelling cells. The ECM is a fundamental component of the microenvironment of cells exhibiting both cell and tissue type specificity, which facilitates cell biological functions and defines tissue properties. Concisely, the ECM components provide the mechanical and structural support as they define the size, morphology and strength of tissues in vivo . Additionally, this polymer-based microenvironment is also important during growth, development, and wound repair as well as key to various disease processes. Therefore, it acts as a pool for signaling molecules including inflammatory mediators, transporting signals from other origins to proliferating, differentiating and migrating cells [5,6,7].
The evolution of nanotechnology and application of nanoparticle (NP) based materials in medicine have opened a new era in diagnosis and treatment improvement for several health issues. Considering the scanty amount of information about the inflammatory changes of the ECM interacting with the NPs, this review aims to elucidate the interplay and accumulation of NPs by the ECMs. It will outline key chemical, physical, and biological properties that influence distinctive domains of the neighboring biological barriers and the resultant effects on homeostasis and immune processes.
Basic components of Extracellular matrix and role of inflammation
Historically, the ECM components were defined as inert “mucilage” which surrounds the cells and were thereby placed on the secondary-track of innovative and pioneering research endeavors. During the last decades, however, breakthrough advances in the field have been achieved and these biomolecules are presently acknowledged as indispensable participants in all vital biological processes and nanomedicine applications . Indeed, it is now well established that the biomolecules that constitute the ECM have developed structural and physico-chemical properties that particularly meet the requirements necessary for the execution of their specific biological functions in their individual tissues. Thus, these macromolecules are composed of independent structural domains which in turn form homopolymers and heteropolymers that become supramolecular assemblies with highly specialized structure and functions [2, 8]. The domain organization of ECM molecules may be correlated to conserved structure–function relationships, including the binding of specific integrin or non-integrin receptors by fibronectin, fibrillation of collagen or its decoration by mediator-binding small leucine rich proteoglycans thereby affecting the topical concentration or availableness of these factors [4, 9]. These assemblies thus, contain binding domains for different cytokines as well as ligands for canonical growth factor receptors, form complex adhesion/interacting surfaces and create diffusion boundaries between neighboring biological layers [8, 10]. In summary, each class of ECM molecules has developed unique physical and signaling properties which enable interaction with other ECM components to ultimately facilitate correct tissue organization, growth and function .
The two basic structures of the ECM are basement membranes, which are organized as thin layers of highly crosslinked biomolecules, and the loose array of fibril-like macromolecules which in fact form the interstitial matrix. Specifically, the interstitial matrix is a complex composed of the collagens organized as fibrils (such as collagen types I, II, III, V and XI), which provide plasticity and tensile strength and of non-collagenous glycoproteins (such as tenascin, fibronectin, chondroitin/dermatan sulfate containing proteoglycans), which are highly negatively charged molecules with an outstanding capacity for intermolecular interactions with other ECM components and cytokines  (Fig. 2). Pericellular matrices, are a very narrow zone found in the immediate vicinity of cells, with specific characteristics. This region has been shown to be rich in proteoglycans (e.g., aggrecan and decorin), collagen (types II, VI, and IX), fibronectin and hyaluronan but is defined primarily by the presence of type VI collagen .
The basal membranes are organized layers of cell-adherent ECM molecules that form supporting platforms for “anchored cells” including epithelial, muscle, nerve as well as endothelial cells [13, 14] (Fig. 3). They are mostly formed of collagen IV and VII crosslinked polymers, heparan sulfate containing proteoglycans as well as laminins bound to basement membrane protein, nidogen . These “sheet-like” structures are formed early during embryogenesis in order to segregate developing tissues, function as macromolecular filters and provide sites for cell adhesion . Importantly, the basal membranes shield tissues from deleterious biological stresses while concurrently facilitating dissemination of information among cells residing in the tissue and between cells and their exterior microenvironment [13, 14]. Furthermore, highly specialized ECM structures with features common to the basement membrane and the interstitial matrix, create the reticular fiber web of secondary lymphoid organs .
The ECMs are essential for tissue homeostasis while their remodeling is closely correlated to different pathological conditions including inflammation, cancer and toxicity related to xenobiotics [6, 16, 17]. A significant number of reports testify to an important role of ECM in inflammatory processes [18,19,20]. Indeed, it is widely accepted that ECM regulates various features of the inflammation process including the extravasation of leukocytes and their subsequent migration through the interstitial space . Then again, in inflamed tissues, both the turnover of ECM components and the secretion of proteases by cells residing in tissues are regulated by cytokines that are secreted by the activated infiltrating cells . There are strong indications in favor of the fact that ECM breakdown products are not only the consequence of inflammation, but also key players in the protraction of the inflammatory process. Changed expression of ECM molecules can in turn affect the activation, differentiation and survival of immune cells, and thus ultimately influence the extension of the inflammatory response and the evolvement of a chronic course . Understanding the interaction of ECM and inflammatory processes is pivotal for medicine as most diseases are associated with secondary inflammatory mechanisms (e.g. ischaemia or metabolic diseases).
Extracellular matrix and nanoparticles interactions
It is now increasingly recognized that NPs interact with the complex suprastructure of the ECM [21, 22]. Moreover, the territorial, immediately surrounding cell region of the ECM, the pericellular matrix, may have an important contribution in the interplay among NPs and various biological barriers. NPs are materials with novel physico-chemical properties classified due to their size, structure and surface chemical modifications. Indeed, the European Union published a definition on nanomaterials (2011/696/EU) which was adopted by the European Commission in October 2011. “The published Recommendation on the Definition on Nanomaterials defines nanomaterial as a natural, incidental or manufactured material containing particles, in an unbound state or as an aggregate or as an agglomerate and where, for 50% or more of the particles in the number size distribution, one or more external dimensions is in the size range 1 nm-100 nm (2011/696/EU).” . NPs are influenced by components of the ECM in three ways: (i) they collide with matrix fibers as they diffuse near fibers, (ii) restricted thermal motion of water molecules due to proximity to the fibers slows NPs’ diffusion (hydrodynamic interactions), and (iii) for charged particles, electrostatic interactions with charged components of the ECM present an additional, limiting force .
NPs interact with the biological system, often leading to the induction of inflammatory or allergic reactions, as well as to activation of the complement system  on one hand. On the other hand, NPs play the role of carrier and adjuvant, with the immune response being dependent on size and crystallinity . Transport of the NPs through the ECM is more complicated due to its’ inherent mesh-like organization . The combined density of all participating biopolymers sets the physical properties of matrix. Particles with diameters larger than the size of network space are rejected by ECM, while smaller particles are able to pass through the matrix barrier . Furthermore, it is well-known that changes in the microenvironment and the ECM surrounding the cells can profoundly influence signal transduction events into and out of the cells . The 20–40 nm spacing between collagen fibrils block the migration of larger particles. Additionally, inter-fibrillar spacing, 75–130 nm around the compact collagen bundles or within loose bundles hampers the diffusion sets another limit for particle size . Noteworthy, the alignment and spacing of collagen fibrils is arranged by proteoglycans. The space among the collagen fibrils is determined by dermatan/chondroitin sulfate or keratan sulfate chains bound into the protein cores of small leucine rich proteoglycans. The proteoglycan protein cores bind to the specific binding domains of collagen fibrils at approximately every 65 nm while their sulfated side chains bridge and determine the inter-fibrillar space . Likewise, the basement membrane hinders the diffusion of NPs in a manner dependent on their size. Indeed, the specialized network of ECM proteins substantially affect the transmucosal transport of NPs . Thus, it is important to note that the ECM components -NPs interactions are dependent on their respective intrinsic properties . As regarding the ECM components, although the size of glycosaminoglycan chains is a few nanometers, their effect is important. Thus, negatively charged chondroitin sulfate content of the ECM, restricts uptake of NPs. The charge of NP as well as the charge of the ECM components are critical for trafficking and uptake of NPs . In contrast, for larger fibers such as collagen, the effect of repulsive forces becomes less significant. Also, when comparing the parallel and transverse to the preferred fiber direction diffusion coefficients to the preferred fiber direction it was demonstrated that the mobility of charged particles is affected more in the transverse direction . Therefore, the complex ECM hydrogel can be interpreted as a network with localized charge patches. These patches in the ECM are responsible for its highly unspecific but strongly selective filtering effect for NPs . Regarding the modulation of other biological functions, it can be noted that molecular spacing is also important for cell adhesion . Cells adhere well to nanopatterned agrin, which is a heparan sulfate proteoglycan, when presented as uniformly coated substrate. However, there is a threshold for the distance between the NPs to facilitate the adhesion. The adhesion dramatically decreases when the space between agrin-coated NPs broaden from 60 to 90 nm. This shows that cell adhesion to nanopatterned substrates primarily corresponds to the interactions with the ECM rather than to the transmembrane adhesion . All cells with exception of blood cells have the ability to adhere onto the components of the surrounding ECM . In summary, one aspect of the interaction of the ECM and NPs is the filtering effect of the relatively densely structured ECM with its distinct charge properties. Thus, very small NPs with a size less than 20 nm may not be hindered and may therefore exhibit a higher toxicity risk. Thereby, the data discussed likely suggests that NP effects on cells can be modulated in a location specific manner by the constituents of the surrounding ECM.
Toxicity of nanoparticles to cells and ECM components
The size of NPs determines their toxicity to a large extent. Indeed, an inverse relation between particles smaller than 100 nm and their toxicity has been established with the NPs inducing a time- and dose-dependent decrease in cell viability. Moreover, the agglomeration of NPs results in altered mechanical properties . In addition to size, the shape and charge of the NPs contribute crucially to the behavioral characteristics of particles in the biological systems [36,37,38]. In this respect, carbonate form layered double hydroxide NPs that are anionic lamellar compounds made up of positively charged brucite-like layers, exhibit higher toxicity compared with the chloride form in terms of induction of oxidative stress, apoptosis and membrane damage [39, 40]. The chemical surface structure of the amorphous silica NP (aSNP) defines the toxicological outcomes of the particle. Upon aspiration, the aSNP attaches to the negatively charged alveolar surfactant layer with a thickness of 10 to 20 nm. The ECM protein microfibril-associated protein (MFAP4) binds the collagen-like region of surfactant protein-D (SP-D). MFAP4 may fix the Sp-D in the extracellular compartment during NP induced inflammation . Moreover, aSNP-NH2 causes a moderate toxic effect, while the carboxylated form does not appear to be cytotoxic. However, a significantly augmented interleukin-8 (IL-8) release is observed in the latter case, indicative of immune activation . The uptake and interaction of the NPs with the cells are, however, not only affected by their surface charge, but also by respective ligands. Thus, the coupling of ligands on the surface of NPs can facilitate the cellular binding . The number of coated human serum albumin molecules per NP is likewise influenced by their surface charge. Thereby, positively charged NPs are incorporated by cells to a larger extent than negatively charged ones, both in serum-free and serum-containing media . On the other hand, hyaluronan a highly negatively charged glycosaminoglycan component of the ECM strongly attracts the citrate-gold NPs [45, 46]. Electrostatically stabilized citrate-coated very small superparamagnetic iron oxide particles (VSOP) bind to the cell surface with high affinity. However, inhibition of glycosaminoglycan synthesis by glucose deprivation in THP-1-derived macrophages is associated with a significant reduction of VSOP linkage. This effect is due to the high affinity of VSOP for the negatively charged glycosaminoglycans which are localized to the cell surface . In addition, NPs can be modified with amphiphilic polymers which results in obtaining NPs of different charge but, with otherwise identical physical properties. While the protein-cationic NPs complex binds to cell surface scavenger receptors, the protein-anionic NPs complex binds to native protein receptors .
AgNPs composite nanofibers accelerate the rate of collagen production in comparison to plain collagen nanofibers, during wound repair . Likewise N-acetylcysteine S-nitrosothiol NPs attenuate wound expansion and accelerate wound healing by increasing collagen deposition, as well as increasing M2 macrophage and decreasing neutrophil infiltration to the wound . While the M1-polarized macrophages are involved in pro-inflammatory response, M2 macrophages exhibit an anti-inflammatory property during wound-healing. Furthermore, NP-mediated delivery of interferon regulatory factor 5 (IRF5) siRNA results in the resolution of inflammation by decreasing the recruitment of M1 macrophages and promoting the polarization of macrophages into M2 type in the wound . NO-releasing NPs modify leukocyte migration and stimulate transforming growth factor-β (TGF-β) production, resulting in the subsequent promotion of angiogenesis, as well as the migration of fibroblasts and collagen deposition in wounded area resulting in accelerated wound healing  (Fig. 4).
In general, the risk of toxic effects of NPs increases with decreasing size, positive charge and fiber-like shape. In addition, surface ligands may be important for activation of the immune system. Therefore, it is of outmost importance to correctly correlate the fine modulations of NPs inherent characteristics with their biological effects.
Nanoparticles and cell membrane interaction
The plasma membrane of the cells contains microdomains that are enriched in certain glycosphingolipids, gangliosides, and cholesterol that form membrane/lipid rafts. Membrane/lipid rafts have myriad functions including the regulation of cellular polarity and organization of trafficking and sorting mechanisms. These rafts are also important for forming platforms for ECM adhesion and intracellular cytoskeletal binding to the plasma membrane and for adherence to the ECM. Furthermore, they are involved in generation of signaling events and constitute the sites where NPs enter the cells .
Sphingolipid metabolites, ceramide, sphingosine, and sphingosine 1-phosphate (S1P) are known to act not only as intracellular second messengers, but also serve as important mediators in the extracellular space with the S1P binding to the cell surface S1P receptors . Particle properties triggering intracellular reactive oxygen species (ROS) may be considered as determining factors for the subsequent adverse signaling. Pure carbon NPs are known to generate ROS due to their high surface area and the specific surface reactivity . Oxidative stress can lead to cell dysfunction or cell death and can induce damage to the ECM . Generation of intracellular oxidative stress as the initial event in a cascade of membrane signaling events involving the accumulation of sphingolipid metabolites in lipid rafts and the activation of the membrane-coupled epidermal growth factor receptor (EGFR) . The most well-known localization of EGFR is to lipid rafts, which are enriched in cholesterol, sphingolipids and gangliosides . Autophosphorylation of EGFR leads to the activation of two downstream pathways: The mitogen-activated protein kinase (MAPK) pathway and the phosphatidylinositol 3-kinase/ protein kinase B (PI3K/Akt) pathway. The major MAPK pathways consist of extracellular signal-regulated kinase (ERK)1/2, p38 and c-Jun N-terminal kinase (JNK) . On the other hand, plasma low density lipoproteins (LDLs) complexes can be defined as native 20- to 25-nm NPs, which bind to the ECM proteoglycans in the arterial intima induce hydrolytic and oxidative modifications . The interaction of LDL and lipoprotein lipase with four atheroma constituents, namely, smooth muscle cells, ECM, lipoprotein lipase and sphingomyelinase, represents a physiological process for solid, focal retention and aggregation of atherogenic lipoproteins in the arterial wall accompanied with macrophage foam cell formation .
NP-cell membrane interactions may affect the localization of the NPs, their intracellular trafficking, compartmentalization into various parts of the organism, and cellular retention . Poly(dl-lactide co-glycolide, PLGA) NPs functionalized with poly-l-lysine adhere to the human breast carcinoma cell membrane with five-fold greater affinity and are rapidly internalized compared with the unmodified NPs . In addition, the density of the NPs’ cationic charge, lipid bilayer’s negative charge load, surface tension, temperature, and salt concentration influences the capacity of particle to form a membrane “hole”. Cationic particles cause the formation of disintegrated surface unity in the bilayer and hydrophilic pores, allowing thus, the cationic NPs more readily penetrate through cellular membranes compared to the anionic counterparts . Cationic lipid/DNA complexes (lipoplexes) are engulfed into cells by endocytosis or direct penetration through the cell membrane, following the association of the cationic lipopolyamines with membrane proteoglycans. Endosome–lysosome transition is delayed via the acidification of endosomes that is slowed down by the protonable amine groups of lipoplexes . On the molecular level, the membrane proteins can be rearranged laterally. The conformational changes regulate the activity of these proteins. In addition, mechanical forces modulate the properties and the binding capabilities of receptor-ligands . Thereby, NPs can also alter the plasma membrane organization by interaction with membrane-bound proteins. Thus, binding of the NPs to reduced nicotinamide adenine dinucleotide phosphate (NADPH)-oxidase (NOX) leads to generation of ROS and intracellular Ca2+ changes. Calcium promotes activation of NP-treated macrophages leading to the release of intermediates that activate intercellular adhesion molecule-1 (ICAM-1) and IL-8 expression in epithelial cells . Amorphous SNP closely interacts with soluble serum proteins, as well as cellular membrane, resulting in more pronounced oxidative stress and pro-inflammatory effects in macrophages .
Here we also observe a dependence of the membrane-NPs interactions on the NPs size. Thus, although AuNP of 20 nm (AuNP20) could be internalized in cytosolic vacuoles, AuNP70 are restricted to the cell membrane. However, both particles induce apoptosis via caspase-dependent mechanisms. AuNPs induce degradation of the cytoskeletal proteins vimentin, lamin B1 and gelsolin .
Histidine rich glycoprotein is a widely distributed plasma alpha2-glycoprotein that interacts with ligands such as Zn2+, haem, tropomyosin, heparin, heparan sulfate, plasminogen, plasmin, fibrinogen, thrombospondin, IgG, FcgammaR and complement protein 1q (C1q), thereby modulating essential biological functions including the regulation of cell adhesion, migration, fibrinolysis, coagulation, complement activation, clearance of the immune complexes, as well as clearance of the apoptotic cells . Histidine rich glycoprotein is a modular protein consisting of an N-terminal cystatin-like domain (N1 N2), a central histidine-rich region flanked by proline-rich sequences, and a C-terminal domain. The N1 N2 domain binds to cell-surface heparan sulfate. The histidine-rich region facilitates the cell-surface binding capacity by interacting with Zn2+ . This glycoprotein is found in excessive amounts in human plasma and constitutes the most abundant element of the SiO2-NP hard corona. The depletion of histidine rich glycoprotein and kininogen-1 from human plasma or their exhaustion in plasma by the increase of NP concentrations lead to a heterogeneous hard corona which is mostly formed by fibrinogen, high density lipoproteins, LDLs, IgGs and kallikrein, which ultimately allows the binding of NPs to macrophages . This is another example of a constant and dynamic interaction between the NPs and their microenvironment with immediate effects on NPs biological actions.
Well known heterodimeric membrane glycoproteins, integrins, consist of non-covalently associated alpha and beta subunits. These contact points modulate the attachment of the cells and their migration on the surrounding ECM. Integrins also regulate the cell to cell interactions under both physiological and pathological conditions affecting key biological functions such as proliferation, differentiation and apoptosis . Ultrafine particle-induced proliferation is modulated by the activation of beta1-integrins that is mediated also through the EGFR signaling. The redirection of the cell into apoptotic or proliferative pathways is triggered via the modulation of interaction of EGFR and Bcl-2. Downstream of EGFR, the activation of MAPK ERK 1/2 promotes proliferation in a manner dependent on beta1-integrin, whereas on the other hand, the phosphorylation of JNK 1 and 2 is associated with the induction of apoptosis . NP-induced proliferation can be mediated by PI3K and Akt. Moreover, overexpression of a variant type of Akt, and pretreatment with an Akt inhibitor, reduces NP-specific ERK1/2 phosphorylation. Thus, the resultant effect is the promotion of the NP-induced proliferation. The activation of a pathway by carbon NPs is triggered by ligand receptor binding or on cell adhesion to ECM proteins . Akt plays an integral role in a wide range of intracellular signaling pathways that are mainly initiated by a variety of extracellular signals. As mentioned above, these signals are transferred via several classes of membrane-bound receptors . Thus, when recognizing and interacting with cell membrane receptors, NPs can induce directly or indirectly activate intracellular pathways, via ECM proteins or kinases . Additionally, exosomes, extracellularly secreted membrane vesicles that measure 30 to 100 nm in diameter, function in intercellular signaling by transporting different membrane and cytosolic molecules, including hyaluronan and its synthesis machinery . They are also involved in transferring genetic materials, and modulation of immune response. Evidence indicates that they can be used as not only therapeutic agents targeted against disease but also diagnostic biomarkers for pathologic conditions . Actually, NP-induced exosomes are signaling mediators, which provoke the activation of T helper cell type 1 and inflammatory responses .
Macrophages are a type of immune cells that engulf and digest cellular debris, foreign substances, microbes, as well as cancer cells. Thus, they are also the “first responders” to NPs . NP uptake is enhanced in M2-polarized primary human monocyte-derived macrophages compared to the M1 cells. M2 polarization promotes the NP uptake in the monocytic THP-1 cell line . Rapid recruitment of macrophages is triggered by the activation of the complement system within injured tissues, such as in wounds and burns, by antigen/antibody (Ag/Ab) interaction. Such activation results in generation of chemotactic complement cleavage peptides, including C5a and C3a which induce extravasation of blood monocytes and maturation of these monocytes into macrophages . Alpha-galactosidase is a glycoside hydrolase enzyme that is widely distributed in human. Alpha-galactosidase (Alpha-gal) NPs prepared from glycolipids with multiple alpha-gal epitopes, phospholipids, and cholesterol, cause extensive macrophage recruitment. Recruited macrophages reach Alpha-gal NPs as the result of interaction between the Fc “tails” of anti-Gal coating Alpha-gal NPs coated Alpha-gal NPs and FcgammaR on these macrophages. The binding of Alpha-gal NPs to macrophages via Fc/FcgammaR interaction activates macrophages. These NPs may further be incorporated into biodegradable scaffold materials such as natural or recombinant collagen sheets, dressings . As anti-Gal ubiquitously present in humans, activation of the recruited macrophages by interaction with anti-Gal coated Alpha-gal NPs may induce angiogenesis, fibroblast migration, collagen deposition and effective recruitment of stem cells  (Fig. 4). Indeed, platelet-derived growth factor (PDGF)-AA, PDGF-BB, EGF, TGF-β1, monocyte chemoattractant protein-1 (MCP-1), interferon gamma (IFN-γ)-induced protein-10 (IP-10), IL-1α, IL-1β, and IL-15 are effective on both type I collagen and hyaluronan production in ECM remodeling. Some chemokines, such as MCP-1 (CCL2), regulates on activation, normal T cell expressed and secreted (RANTES; CCL5), eotaxin-2 (CCL24), IP-10 (CXCL10), or fractalkine (CX3CL1) significantly induce the type I collagen or hyaluronan production . Overexpression of the recently identified glycophosphatidylinositol-anchored protein CD109, a novel TGF-β co-receptor and inhibitor of TGF-β signaling, has been shown to reduce inflammation and improve collagen organization in wound granulation tissue . Indeed, TGF-β is an indispensable cytokine in tissue fibrosis. Despite both direct wound-healing and antibacterial effects of AgNPs, it has been shown that AgNPs do not induce TGF-β production . Furthermore, AgNPs are predominantly responsible for regulating deposition of collagen and they generate an excellent alignment in the healing process . These particles are deposited mainly to the terminal bronchial/alveolar duct junction region of the lung where they interact with ECM and also with the epithelial cells, independent from the particle size. However, treatment with smaller particles, 20 nm AgNPs, results in an elevated silver burden in bronchoalveolar lavage fluid macrophages . The citrate-coated VSOP binds strongly to the cell surface, as well as to the apoptotic membrane vesicles in a manner dependent on hyaluronan expression. Since, hyaluronan synthesis is largely dependent on glucose levels, in a microenvironment where glucose is low, negatively charged hyaluronan synthesis decreases, attenuating the VSOP attachment to THP-1-derived macrophages .
Increased fibroblast proliferation and collagen synthesis are the cardinal signs of fibrosis. PDGF, synthesized by the macrophages is a potent mitogen and acts as chemoattractant for fibroblasts. The extent of the responsiveness of fibroblasts to PDGF is modulated by the proportion of cell surface PDGF receptor α (PDGF-Rα) number relative to the PDGF-Rβ number. The PDGF-Rα is upregulated by IL-1β which stimulates the expression of PDGF-AA, PDGF-AB, and PDGF-BB isoforms and ultimately promotes the lung fibroblast proliferation. Even though, both IL-1β and TGF-β1 are synthesized via the particle-stimulated macrophages, TGF-β1 has opposing effects. The macrophages treated with TiO2, chrysotile asbestos, or residual oil fly ash have 3-, 6- and 20-fold enhanced binding capacity to PDGF-AA, respectively. These NP-activated macrophages initiate fibrotic response by increasing fibroblast PDGF-Rα expression via IL-1β . The remodeling of ECM is largely mediated by fibroblasts as the major cell type controlling ECM network. Innate cytokine responses may be critical in non-allergic/non-autoimmune disease, and they enable environmental agent exposure mechanisms that are independent of adaptive immunity . Pulmonary alveolar macrophages may participate in the pathogenesis of acute inflammatory lung injury by the secretion of monocyte chemoattractants including MCP-1 . Monocyte chemotactic protein-1-induced protein 1 (MCPIP1) plays a critical role in fibrosis induced by SiO2. MCPIP1 promotes the autophagic process in macrophages in response to silica exposure. Enhancement of macrophage autophagy further increases the pro-fibrogenic stimulatory effect. Eventually, macrophages act as paracrine effectors to modulate fibroblast proliferation and migration and macrophage autophagy plays a central role in these effects . Accumulation of carbon nanomaterials in macrophage lysosomes, leading to lysosome membrane destabilization, indicates reduced autophagic degradation. This process is suggested to be a potential mechanism of the toxic effects of nanomaterials on cells .
In summary, NPs can recruit macrophages, activate them and are taken up by these immune cells. In some cases, autophagy of macrophages can be enhanced. Via activation of macrophages and subsequent fibroblast proliferation, NPs can indirectly re-model the ECM. These data indicate that a feedback mechanism involving macrophage and fibroblast responses which are mediated through ECM-dependent signaling determines NPs’ toxic effects in some tissue types.
The role of extracellular matrix metalloproteinases in nanoparticle induced immune response
ECM matrix metalloproteinases (MMPs) are a family of zinc-dependent neutral endopeptidases. They are designated to degrade all matrix components, and are thereby involved in both physiological and pathological conditions . Thus, MMPs act as extracellular proteases that modulate, for example, the immune response in pulmonary inflammatory processes. In the case of Cryptococcus infection the MMP-12 levels are strongly correlated with the expression of the macrophage- and neutrophil-attracting chemokine CCL2 mRNA . It is noteworthy that TiO2 NPs induce the expression of elastase-induced MMP-12 mRNA in the lung  and in murine macrophages . Carbon black (CB) NPs induce perivascular or peribronchial infiltration, increase inflammation and expression of the oxidative stress marker heme oxygenase-1 (HO-1) mRNA in ECM and increase the protease MMP-12 mRNA, as well as protein expression in alveolar macrophages. These particles also aggravate elastase-induced perivascular or peribronchial inflammation . However, TiO2 and CB NPs elicit distinct apoptotic pathways  and oxidative stress, that can be determined by the elevation of the HO-1 expression and MMP-12 stimulation following the CB NPs exposure, but not after the TiO2 NPs treatment . After incubation with 7 nm ultrafine TiO2 particles for 1 day, the expression of MMP-9 and MMP-10 genes and cell-matrix adhesion molecules, fibronectin-1, integrin subunit beta-6, and mucin-4 are altered in keratinocytes . Furthermore, both AgNPs with a diameter of 20 nm (AgNP20) and AgNPs with a diameter of 70 nm (AgNP70) inhibit de novo protein synthesis. Both forms of AgNPs do not significantly affect ROS production, but AgNP20 significantly increases the CXCL8 chemokine (IL-8) generation. In addition, AgNP20, but not AgNP70, induce the release of albumin and MMP-9/gelatinase B . When treated with AgNP20, the size of the neutrophils increase and transmission electronic microscopy results indicate that within 1 day of exposure, AgNP20 can rapidly interact with the cell membrane, penetrate into neutrophils, localize in vacuole-like structures, and are randomly distributed in the cytosol . The cellular MMPs and tissue inhibitors of matrix proteases (TIMPs) strictly regulate the integrity of generated matrix at three distinct stages of elastic matrix synthesis . Thus, TIMP-1 as an endogenous inhibitor of MMPs is capable of regulating the cleavage of ECM components, as well as membrane and secreted proteins. MMP-1 is an important factor in matrix homeostasis and involved in TiO2 NP associated effects. Thus, TiO2 NPs potentially stimulate and also modulate the MMP-1 expression and activity, partly through an IL-1β-dependent pathway . Indeed, during inflammation and connective tissue destruction, IL-1β acts as a central mediator and also activates articular chondrocytes resulting in the release of MMP-1. In some diseases this involves connective tissue deregulation as IL-1β activated MMP-1 dismantles the collagen scaffold .
Fibrosis develops as the result of the abnormal accumulation of the ECM and ineffective clearance of fibroplasia. CD4+CD25+Foxp3+ regulatory T cells (Tregs) are immunosuppressive lymphocytes that are highly expressed in the fibrotic tissues. The expression of MMPs and TIMPs is altered depending on the depletion of Tregs; MMP9 and TIMP1 are decreased, whereas MMP2 and MMP14 are increased. Nevertheless, the MMP9/TIMP1, MMP13/TIMP1, and MMP14/TIMP2 are markedly elevated in association with resolution of fibrosis . Survival of the Treg subset is dependent on the cytokines IL-2 and TGF-β whose syntheses are impaired in autoimmunity. In the pro-inflammatory microenvironment, the conversion of Tregs into effector cells is enhanced. Inert biodegradable NPs loaded with TGF-β and IL-2 and targeted to CD4+ cells can induce CD4+ Tregs conversion, in vitro and expand the CD4+ Treg population, in vivo . However, the survival rate of induced Tregs with cytokine-loaded NPs are prolonged leading to retention of their suppressive phenotype even in the presence of proinflammatory mediators . In addition to the effects on Tregs, the excessive bioavailability of TGF-β promotes elastic matrix synthesis. Furthermore, TGF-β1 and hyaluronan oligomers together induce much greater assembly of mature elastin fibers when provided concurrently . Cerium oxide (CeO2) NPs also interact with the MMPs regulation. These NPs, introduced to lung epithelium through diesel exhaust exposure, significantly increase fibrotic cytokine TGF-β1 and osteopontin production by alveolar macrophages. Upon exposure to NPs, the collagen degradation enzymes, MMP-2 and -9 and the TIMP markedly increase. Moreover, CeO2 induces increment in phospholipids in bronchial alveolar lavage fluid and elevates hydroxyproline content associated with collagen fiber deposition in lung tissue in a dose- and time-dependent manner. Eventually MMP-2, MMP-9 and MMP-10 expressions increase in fibrotic regions . Although, amorphous SiO2 (aSiO2) and CeO2 particles induce a dose-related inflammation, cytotoxicity, inflammatory cytokines, MMP-9, and tissue inhibitor of MMP, aSiO2 coating significantly reduces CeO2-induced inflammatory responses and attenuate phospholipidosis and fibrosis . So far, experiments regarding the NPs, MMPs, TIMPs and immune response show an irregular picture because many different players interact with each other. Mainly, for metal-based NPs it has been shown that they increase chemokine concentration which in turn can influence sub-groups of MMPs which then may remodel the ECM in one or the other way depending on the specific MMP sub-group and the presence of different chemokines or cytokines. In summary, NPs-dependent signaling may seriously impair the ratio between MMPs and TIMPs which results in pathological turn-over of the ECM and facilitation of inflammatory processes.
Lysyl oxidase crosslinking of elastin matrix and nanoparticles
Elastin, a fibrillar protein, is a key component of the ECM surrounding smooth muscle. The formation of the mature elastin fiber in the ECM demands the organization of its soluble precursor molecules, designated as tropoelastin, into a polymer characterized by a high level of crosslinking. The tropoelastin molecules however, do not have the innate ability to self-assemble but need helper proteins to correctly assort their multiple crosslinking sites to facilitate this process. Thus, versican, a large ECM proteoglycan in collaboration with hyaluronic acid, plays a key role in elastin precursor recruitment and fiber assembly. The precise interaction of this helper protein with tropoelastin molecules is favoured by its highly anionic nature enabling it to bind to oppositely charged regions of tropoelastins . Indeed, the tropoelastin molecules are assembled from mostly hydrophobic amino acids, with lysine containing hydrophilic domains. The hydrophilic lysine residues play an important role in the crosslinking of tropoelastin molecules, which is a critical step of the elastic matrix assembly process . In this context, lysyl oxidase (LOX), a copper-dependent amine oxidase plays an important role in the stability of the elastic matrix by catalyzing the crosslinking of tropoelastin into mature elastic fibers . NPs cause a significant increase in LOX production . The increase in LOX production is consistent with desmosine crosslinking of elastin . Thus, increased crosslinking of elastin precursors is responsible for the increased deposition of elastic matrix. Interestingly, PLGA NPs encapsulated with varying percent loadings of hyaluronan oligomers induce dose dependent increase in elastic matrix synthesis. Furthermore, these NPs enhance LOX production, and lead to improved deposition of a microfibrillar network . Elastin matrix deposition stimulation by Cu2+ ions and enhanced crosslinking via stimulation of LOX simultaneously occur in hyaluronan and copper NP-treated elastin matrix  (Fig. 5). Therefore, the targeting of elastin matrix by specific NPs can improve its stability that is crucial in human disease as is the case of vascular inflammation .
Interaction of nanoparticles with biological barriers
During the ontogeny of cavity containing tissues, an ECM-dependent mechanism orients and polarizes the cells in the tissue, in order to obtain phenotypes that support physiological functions. The epithelium and its’ specialized subtype, the endothelium, are lining the body’s cavities and blood vessels, including the blood-brain barrier. They represent the main trafficking avenues studied in nanomedicine. Furthermore, NPs were characterized in terms of dimensional analysis, polydispersity and zeta potential, morphology, encapsulation efficacy, and loading capacity . It is noteworthy that basal membranes, the highly specialized ECM structures, are crucial components of all biological barriers [2, 4, 10].
The epithelium represents a monolayer comprised of cells that delineate a cavity or even a surface. In this type of tissue, the cells have a distinct 3D orientation. They have an apical type of plasma membrane that is fronting the lumen or the surface, a plasma membrane that has a lateral position touching the surrounding cells, and a plasma membrane at the base, contacting the basal membrane, constituting highly specialized form of ECM. This specific orientation is synchronized between the cells that form the tissue, namely the cavity where the apical plasma membranes of neighboring cells are radially polarized. The main mechanisms for cell polarization are sustained by the interaction of cells with ECM and with the surrounding cells .
Recently, it was shown that defects in ECM signaling induce an inverted polarity between apical surfaces and surfaces facing the ECM. Thus, in a Madin Darby Canine Kidney (MDCK) epithelial cellular in vitro model, it was reported that there is a molecular switch that actually controls the polarity orientation. At the ECM/cell interface signals are generated which involve a b1-integrin/FAK/p190RhoGAP complex that down-regulates the RhoA/Rho-associated protein kinase/Ezrin (RhoA/ROCK/Ezrin) pathway . In this manner, podocalyxin, a protein important for cell polarity orientation  is removed from the cell surface adjacent to ECM and transcytosed to the apical membrane where there is the initiation site for lumen formation. Transcytosis occurs when membrane-bound carriers transport molecules in a selective manner between one part of the cell to another. Inhibition of this mechanism retains podocalyxin at the ECM interface and disturbs polarization and motility. Collective orientation and epithelial polarization are controlled by ECM-derived signals . Importantly, this mechanism may be utilized for NP transport. The mechanics of transport is seminal for several systems inducing, epithelial-based tissue and hepatocyte barrier. Small molecules can be transported either transcellularly or paracellularly, while macromolecules and NPs use transcytosis (Fig. 6).
Transcytosis is used by the epithelial cells in the immune processes, in nutrient absorption, and plasma membrane biogenesis. Endothelium and cells of the endocrine system also rely on transcytosis processes .
The endothelium barrier, consisting of microvascular endothelial cells at blood-vessel interface, controls the essential functions of body organs, regulating the volume of tissue fluids and supply of nutrients for homeostasis. Indeed, the endothelial cell may be characterized as a cellular antenna that is sensitive to signals/factors generated in the blood, to the basal membrane, to the sub-endothelium, as well as to the interacting cells. Endothelial cells are distinct from epithelial cells due to their semipermeable characteristic. This characteristic is necessary for the continuous controlled paracellular and transcellular pathways that need a transendothelial protein gradient (colloid osmotic gradient). At this level, interendothelial junctions (IEJ) have proteins that pair to specific ECM components and have the role of limiting the transport of plasma proteins by paracellular pathways. Endothelial cells have an abundant expression of integrins that are actually receptors for subendothelial ECM proteins. At the sites where integrins link to ECM, focal contacts or focal adhesions sites are generated. The focal contacts in collaboration with IEJ induce cell shape alterations and control paracellular permeability (Fig. 7). Indeed, the endothelial cells continuously remodel ECM in mature vessels by secreting ECM constituents which stimulate angiogenesis and vasculogenesis . When the ECM interaction with integrins is established, endothelial cells do not proliferate and/or migrate and become quiescent, which is an essential characteristic for the endothelial barrier .
Beside other mechanisms, the diameter of the NP is an important attribute to enable NP to overcome the various in vivo barriers including ECM components . In the wide framework of nanomedicine, the mechanism types of endothelial transcytosis, similar to epithelium transport, depend on NPs’ functionalization, size and charge. Thus, endocytic pathway is size-dependent. It is indicative that endothelial cells internalize 20 nm NPs by caveolae-mediated endocytosis, whereas the 40 nm NPs are uptaken through clathrin-mediated internalization and micropinocytosis . Importantly, the sub-endothelial ECM contains molecules that regulate transportation. An illustrating example is the specific activity of polymorphonuclear neutrophil-derived (PMN-derived) and monocyte-derived myeloperoxidase (MPO) which catalyze nitrotyrosine formation, a characteristic trait of vascular inflammation. The MPO molecule is transcytosed and is subsequently concentrated to the subendothelial ECM of vascular tissues. The MPO locates to the ECM then specifically catalyzes the nitration of discrete ECM protein tyrosine residues; the main target protein in this case being fibronectin. Interestingly both unfractionated heparin and its low-molecular weight derivative, enoxaparin, in standard endothelial cells and in rat aortic tissues significantly inhibit MPO binding and protein nitrotyrosine formation. Baldus et al., therefore suggest that “Endothelial transcytosis of MPO confers specificity to vascular ECM proteins as targets of tyrosine nitration” . Another important research topic regarding the endothelium barrier is the study of interchange among migrating leukocytes, ECM components and NPs during inflammation. Thus, upon activation of human neutrophils the resulting generation of NO converts intracellular glutathione (GSH) to S-nitrosoglutathione (GSNO), a biological pool for controlled NO release . Alternatively, NO induced oxidation of ECM components, including fibronectin stimulates neutrophil adhesion to ECM decreasing their migratory abilities . Therefore, a targeted uptake of GSNO to immune cell’s intracellular compartments will stimulate immune response without deleterious side effects to ECM. Nanoformulated GSNO with Eudragit as a carrier was tested on THP-1 human monocytic cell line with beneficial results. The mechanisms for transportation was identified as clathrin- and caveolae-mediated endocytosis .
Hepatocytes, like other epithelia, are organized to perform and control the exchange of molecules between two distinct compartments; hepatic parenchyma and capillary system . Due to the central role of the hepatic parenchyma in the metabolism of xenobiotics, many studies have examined the issue of NP uptake and interaction with the liver tissue . Total hepatic collagen content is specifically reduced by the cationic lipid NPs loaded with small interfering RNA to the procollagen alpha1 gene without detectable side effects. Therefore, this application may be a potentially qualifying therapy for fibrotic liver diseases .
In the same in vitro experimental model HepG2, PAMAM-NH2 dendrimers were used as N-Acetylgalactosamine (NAcGal)-targeted carriers for chemotherapeutic agents. This approach demonstrated that the uptake of dendrimers in HepG2 cells occurs via asialoglycoprotein receptor (ASGPR)-mediated endocytosis  (Fig. 8). The above mentioned interactions of NPs with biological barriers and specifically their basal membrane component, exhibit extraordinary complexity and highlight the necessity for further study.
The focus of the scientific community on the use of nanotechnology for technical and consumer applications and in medical diagnostic and treatment during the last decades has resulted in establishing a substantial database. We need to further deepen our knowledge on the interaction of various NPs with specific biological barriers and compartments in optimizing internalization and site specific drug release. However, although it is clear that the content of the extracellular microenvironment critically affects the behavior of NP and their interaction with biological barriers, there is still limited knowledge about the mechanisms and role of different biomolecules in mediating the interaction of these materials with the assembly of ECM. ECM is a highly organized complex network of structural proteins, proteoglycans and glycosaminoglycans. Alteration in the expression of ECM molecules can ultimately affect the immune cell activation, differentiation and survival. These modifications eventually influence the propagation of the inflammatory response. Depending on the targeted tissue, the NPs encapsulated drugs aim to cross specific barriers, including endothelium, or hepatocyte barrier and, at each of these points, there are discrete interactions of the NPs with ECM components. Thus, functionalization and polarization of the drug carrier NPs with suitable peptides and other compounds concurrently enhances their therapeutic effects, by facilitating the transport and bioavailability of encapsulated agents through the ECM, as well as cellular compartments. Taking into account the continuously growing release of various NPs into the environment there is a demanding necessity to define and categorize ECM/NPs interactions and to examine their relevance regarding toxicity and inflammation in various biological processes. Therefore, future research should be focused on elucidating the molecular transport mechanisms that will provide groundwork for coherent design of more effective nano-carriers, improve their performance and target specific intracellular compartments.
Protein kinase B
Adenosine monophosphate kinase-related kinase
Anti-Galactose alpha 1,3-galactose
Amorphous silica NP
Activating transcription factor-6
Complement protein 1q
- CeO2 :
Epidermal growth factor receptor
Extracellular signal regulated kinases
Food and drug administration
Granulocyte colony-stimulating factor
Granulocyte-macrophage colony stimulating factor
Glutamine sensing regulator 1
Glutathione S-transferase Mu 3
Intercellular adhesion molecule-1
Interferon (IFN)-γ -induced protein-10
Interferon regulatory factor 5
Inhibitor of kappa B
c-Jun NH2-terminal kinases
Liver kinase B1
Mitogen-activated protein kinases
Monocyte chemoattractant protein-1
Madin Darby Canine Kidney
N-Terminal cystatin-like domain
Nicotinamide adenine dinucleotide phosphate
Amino-functionalized mesoporous silica nanoparticles
Plasminogen activator inhibitor-1
Platelet-derived growth factor
PDGF receptor α
Peroxisome proliferator activated receptor gamma co-activator-1alpha
Cytochrome P450 oxidoreductase
- RANTES; CCL5:
Regulated on activation, normal T cell expressed and secreted
Reactive oxygen species
Transforming growth factor-beta
Tissue inhibitors of matrix proteases
- TiO2 :
Regulatory T cells
Vascular endothelial growth factor-A
Very small superparamagnetic iron oxide particles
Karamanos NK, Tzanakakis GN. Glycosaminoglycans: from “cellular glue” to novel therapeutical agents. Curr Opin Pharmacol. 2012;12:220–2.
Mecham RP. Overview of extracellular matrix. Curr. Protoc. Cell Biol. Editor. Board Juan Bonifacino Al. 2012;Chapter 10:Unit 10.1.
Lieleg O, Baumgärtel RM, Bausch AR. Selective filtering of particles by the extracellular matrix: an electrostatic bandpass. Biophys J. 2009;97:1569–77.
Hynes RO. The extracellular matrix: not just pretty fibrils. Science. 2009;326:1216–9.
Rosso F, Giordano A, Barbarisi M, Barbarisi A. From cell-ECM interactions to tissue engineering. J Cell Physiol. 2004;199:174–80.
Sorokin L. The impact of the extracellular matrix on inflammation. Nat Rev Immunol. 2010;10:712–23.
Afratis N, Gialeli C, Nikitovic D, Tsegenidis T, Karousou E, Theocharis AD, et al. Glycosaminoglycans: key players in cancer cell biology and treatment. FEBS J. 2012;279:1177–97.
Rozario T, DeSimone DW. The extracellular matrix in development and morphogenesis: a dynamic view. Dev Biol. 2010;341:126–40.
Nikitovic D, Aggelidakis J, Young MF, Iozzo RV, Karamanos NK, Tzanakakis GN. The biology of small leucine-rich proteoglycans in bone pathophysiology. J Biol Chem. 2012;287:33926–33.
Rowe RG, Weiss SJ. Breaching the basement membrane: who, when and how? Trends Cell Biol. 2008;18:560–74.
Lokmic Z, Lämmermann T, Sixt M, Cardell S, Hallmann R, Sorokin L. The extracellular matrix of the spleen as a potential organizer of immune cell compartments. Semin Immunol. 2008;20:4–13.
Zelenski NA, Leddy HA, Sanchez-Adams J, Zhang J, Bonaldo P, Liedtke W, et al. Type VI Collagen Regulates Pericellular Matrix Properties, Chondrocyte Swelling, and Mechanotransduction in Mouse Articular Cartilage. Arthritis Rheumatol Hoboken NJ. 2015;67:1286–94.
Paulsson M. Basement membrane proteins: structure, assembly, and cellular interactions. Crit Rev Biochem Mol Biol. 1992;27:93–127.
Yurchenco PD. Basement membranes: cell scaffoldings and signaling platforms. Cold Spring Harb Perspect Biol. 2011;3(2):a004911.
Martin GR, Timpl R. Laminin and other basement membrane components. Annu Rev Cell Biol. 1987;3:57–85.
Nikitovic D, Corsini E, Kouretas D, Tsatsakis A, Tzanakakis G. ROS-major mediators of extracellular matrix remodeling during tumor progression. Food Chem. Toxicol. Int. J. Publ. Br. Ind. Biol. Res. Assoc. 2013;61:178–86.
Nikitovic D, Juranek I, Wilks MF, Tzardi M, Tsatsakis A, Tzanakakis GN. Anthracycline-dependent cardiotoxicity and extracellular matrix remodeling. Chest. 2014;146:1123–30.
Nourshargh S, Hordijk PL, Sixt M. Breaching multiple barriers: leukocyte motility through venular walls and the interstitium. Nat Rev Mol Cell Biol. 2010;11:366–78.
Nikitovic D, Berdiaki A, Galbiati V, Kavasi R-M, Papale A, Tsatsakis A, et al. Hyaluronan regulates chemical allergen-induced IL-18 production in human keratinocytes. Toxicol Lett. 2015;232:89–97.
Nikitovic D, Papoutsidakis A, Karamanos NK, Tzanakakis GN. Lumican affects tumor cell functions, tumor-ECM interactions, angiogenesis and inflammatory response. Matrix Biol. J. Int. Soc. Matrix Biol. 2014;35:206–14.
Hansen U, Allen JM, White R, Moscibrocki C, Bruckner P, Bateman JF, et al. WARP interacts with collagen VI-containing microfibrils in the pericellular matrix of human chondrocytes. PLoS One. 2012;7:e52793.
Villone D, Fritsch A, Koch M, Bruckner-Tuderman L, Hansen U, Bruckner P. Supramolecular interactions in the dermo-epidermal junction zone: anchoring fibril-collagen VII tightly binds to banded collagen fibrils. J Biol Chem. 2008;283:24506–13.
Piperigkou Z, Karamanou K, Engin AB, Gialeli C, Docea AO, Vynios DH, et al. Emerging aspects of nanotoxicology in health and disease: From agriculture and food sector to cancer therapeutics. Food Chem Toxicol. 2016;91:42–57.
Stylianopoulos T, Poh M-Z, Insin N, Bawendi MG, Fukumura D, Munn LL, et al. Diffusion of particles in the extracellular matrix: the effect of repulsive electrostatic interactions. Biophys J. 2010;99:1342–9.
Kononenko V, Narat M, Drobne D. Nanoparticle interaction with the immune system. Arh Hig Rada Toksikol. 2015;66:97–108.
Maquieira Á, Brun EM, Garcés-García M, Puchades R. Aluminum oxide nanoparticles as carriers and adjuvants for eliciting antibodies from non-immunogenic haptens. Anal Chem. 2012;84:9340–8.
Mair LO, Superfine R. Single particle tracking reveals biphasic transport during nanorod magnetophoresis through extracellular matrix. Soft Matter. 2014;10:4118–25.
Shah C, Yang G, Lee I, Bielawski J, Hannun YA, Samad F. Protection from high fat diet-induced increase in ceramide in mice lacking plasminogen activator inhibitor 1. J Biol Chem. 2008;283:13538–48.
Pluen A, Boucher Y, Ramanujan S, McKee TD, Gohongi T, di Tomaso E, et al. Role of tumor-host interactions in interstitial diffusion of macromolecules: cranial vs. subcutaneous tumors. Proc Natl Acad Sci U S A. 2001;98:4628–33.
Scott JE, Dyne KM, Thomlinson AM, Ritchie M, Bateman J, Cetta G, et al. Human cells unable to express decoron produced disorganized extracellular matrix lacking “shape modules” (interfibrillar proteoglycan bridges). Exp Cell Res. 1998;243:59–66.
Vllasaliu D, Falcone FH, Stolnik S, Garnett M. Basement membrane influences intestinal epithelial cell growth and presents a barrier to the movement of macromolecules. Exp Cell Res. 2014;323:218–31.
Kharaziha M, Fathi MH, Edris H. Development of novel aligned nanofibrous composite membranes for guided bone regeneration. J Mech Behav Biomed Mater. 2013;24:9–20.
Walters R, Medintz IL, Delehanty JB, Stewart MH, Susumu K, Huston AL, et al. The Role of Negative Charge in the Delivery of Quantum Dots to Neurons. ASN Neuro. 2015;7(4):1759091415592389.
Schaufler V, Czichos-Medda H, Hirschfeld-Warnecken V, Neubauer S, Rechenmacher F, Medda R, et al. Selective binding and lateral clustering of α5β1 and αvβ3 integrins: Unraveling the spatial requirements for cell spreading and focal adhesion assembly. Cell Adhes Migr. 2016;10:505–15.
Wolfram T, Spatz JP, Burgess RW. Cell adhesion to agrin presented as a nanopatterned substrate is consistent with an interaction with the extracellular matrix and not transmembrane adhesion molecules. BMC Cell Biol. 2008;9:64.
Takagi A, Hirose A, Nishimura T, Fukumori N, Ogata A, Ohashi N, et al. Induction of mesothelioma in p53+/− mouse by intraperitoneal application of multi-wall carbon nanotube. J Toxicol Sci. 2008;33:105–16.
Neagu M, Piperigkou Z, Karamanou K, Engin AB, Docea AO, Constantin C, et al. Protein bio-corona: critical issue in immune nanotoxicology. Arch. Toxicol. 2017;91(3):1031–48.
Schaeublin NM, Braydich-Stolle LK, Schrand AM, Miller JM, Hutchison J, Schlager JJ, et al. Surface charge of gold nanoparticles mediates mechanism of toxicity. Nanoscale. 2011;3:410–20.
Baek M, Kim I-S, Yu J, Chung HE, Choy J-H, Choi S-J. Effect of different forms of anionic nanoclays on cytotoxicity. J Nanosci Nanotechnol. 2011;11:1803–6.
Yan M, Zhang Z, Cui S, Zhang X, Chu W, Lei M, et al. Preparation and evaluation of PEGylated phospholipid membrane coated layered double hydroxide nanoparticles. Asian J Pharm Sci. 2016;11:396–403.
Lausen M, Lynch N, Schlosser A, Tornoe I, Saekmose SG, Teisner B, et al. Microfibril-associated protein 4 is present in lung washings and binds to the collagen region of lung surfactant protein D. J Biol Chem. 1999;274:32234–40.
Kasper JY, Feiden L, Hermanns MI, Bantz C, Maskos M, Unger RE, et al. Pulmonary surfactant augments cytotoxicity of silica nanoparticles: Studies on an in vitro air-blood barrier model. Beilstein J. Nanotechnol. 2015;6:517–28.
Kumari A, Yadav SK. Cellular interactions of therapeutically delivered nanoparticles. Expert Opin Drug Deliv. 2011;8:141–51.
Hühn D, Kantner K, Geidel C, Brandholt S, De Cock I, Soenen SJH, et al. Polymer-coated nanoparticles interacting with proteins and cells: focusing on the sign of the net charge. ACS Nano. 2013;7:3253–63.
Dimitrov DS. Engineered CH2 domains (nanoantibodies). MAbs. 2009;1:26–8.
Zhang S, Moustafa Y, Huo Q. Different interaction modes of biomolecules with citrate-capped gold nanoparticles. ACS Appl Mater Interfaces. 2014;6:21184–92.
Ludwig A, Poller WC, Westphal K, Minkwitz S, Lättig-Tünnemann G, Metzkow S, et al. Rapid binding of electrostatically stabilized iron oxide nanoparticles to THP-1 monocytic cells via interaction with glycosaminoglycans. Basic Res Cardiol. 2013;108:328.
Fleischer CC, Payne CK. Nanoparticle surface charge mediates the cellular receptors used by protein-nanoparticle complexes. J Phys Chem B. 2012;116:8901–7.
Rath G, Hussain T, Chauhan G, Garg T, Goyal AK. Collagen nanofiber containing silver nanoparticles for improved wound-healing applications. J Drug Target. 2016;24:520–9.
Landriscina A, Musaev T, Rosen J, Ray A, Nacharaju P, Nosanchuk JD, et al. N-acetylcysteine S-nitrosothiol Nanoparticles Prevent Wound Expansion and Accelerate Wound Closure in a Murine Burn Model. J Drugs Dermatol JDD. 2015;14:726–32.
Li J, Liu Y, Xu H, Fu Q. Nanoparticle-Delivered IRF5 siRNA Facilitates M1 to M2 Transition, Reduces Demyelination and Neurofilament Loss, and Promotes Functional Recovery After Spinal Cord Injury in Mice. Inflammation. 2016;39:1704–17.
Han G, Nguyen LN, Macherla C, Chi Y, Friedman JM, Nosanchuk JD, et al. Nitric oxide-releasing nanoparticles accelerate wound healing by promoting fibroblast migration and collagen deposition. Am J Pathol. 2012;180:1465–73.
Head BP, Patel HH, Insel PA. Interaction of membrane/lipid rafts with the cytoskeleton: impact on signaling and function: membrane/lipid rafts, mediators of cytoskeletal arrangement and cell signaling. Biochim Biophys Acta. 1838;2014:532–45.
Tani M, Ito M, Igarashi Y. Ceramide/sphingosine/sphingosine 1-phosphate metabolism on the cell surface and in the extracellular space. Cell Signal. 2007;19:229–37.
Wilson MR, Lightbody JH, Donaldson K, Sales J, Stone V. Interactions between ultrafine particles and transition metals in vivo and in vitro. Toxicol Appl Pharmacol. 2002;184:172–9.
Demedts IK, Demoor T, Bracke KR, Joos GF, Brusselle GG. Role of apoptosis in the pathogenesis of COPD and pulmonary emphysema. Respir Res. 2006;7:53.
Peuschel H, Sydlik U, Grether-Beck S, Felsner I, Stöckmann D, Jakob S, et al. Carbon nanoparticles induce ceramide- and lipid raft-dependent signalling in lung epithelial cells: a target for a preventive strategy against environmentally-induced lung inflammation. Part Fibre Toxicol. 2012;9:48.
Guéguinou M, Gambade A, Félix R, Chantôme A, Fourbon Y, Bougnoux P, et al. Lipid rafts, KCa/ClCa/Ca2+ channel complexes and EGFR signaling: Novel targets to reduce tumor development by lipids? Biochim Biophys Acta. 1848;2015:2603–20.
Wagner EF, Nebreda AR. Signal integration by JNK and p38 MAPK pathways in cancer development. Nat Rev Cancer. 2009;9:537–49.
Lu M, Gursky O. Aggregation and fusion of low-density lipoproteins in vivo and in vitro. Biomol Concepts. 2013;4:501–18.
Tabas I, Li Y, Brocia RW, Xu SW, Swenson TL, Williams KJ. Lipoprotein lipase and sphingomyelinase synergistically enhance the association of atherogenic lipoproteins with smooth muscle cells and extracellular matrix. A possible mechanism for low density lipoprotein and lipoprotein(a) retention and macrophage foam cell formation. J Biol Chem. 1993;268:20419–32.
Adjei IM, Sharma B, Labhasetwar V. Nanoparticles: cellular uptake and cytotoxicity. Adv Exp Med Biol. 2014;811:73–91.
Vasir JK, Labhasetwar V. Quantification of the force of nanoparticle-cell membrane interactions and its influence on intracellular trafficking of nanoparticles. Biomaterials. 2008;29:4244–52.
Lin J, Zhang H, Chen Z, Zheng Y. Penetration of lipid membranes by gold nanoparticles: insights into cellular uptake, cytotoxicity, and their relationship. ACS Nano. 2010;4:5421–9.
El Ouahabi A, Thiry M, Pector V, Fuks R, Ruysschaert JM, Vandenbranden M. The role of endosome destabilizing activity in the gene transfer process mediated by cationic lipids. FEBS Lett. 1997;414:187–92.
Klotzsch E, Stiegler J, Ben-Ishay E, Gaus K. Do mechanical forces contribute to nanoscale membrane organisation in T cells? Biochim Biophys Acta. 1853;2015:822–9.
Brown DM, Hutchison L, Donaldson K, Stone V. The effects of PM10 particles and oxidative stress on macrophages and lung epithelial cells: modulating effects of calcium-signaling antagonists. Am. J. Physiol. Lung Cell. Mol. Physiol. 2007;292:L1444–51.
Di Cristo L, Movia D, Bianchi MG, Allegri M, Mohamed BM, Bell AP, et al. Proinflammatory Effects of Pyrogenic and Precipitated Amorphous Silica Nanoparticles in Innate Immunity Cells. Toxicol. Sci. Off. J. Soc. Toxicol. 2016;150:40–53.
Noël C, Simard J-C, Girard D. Gold nanoparticles induce apoptosis, endoplasmic reticulum stress events and cleavage of cytoskeletal proteins in human neutrophils. Toxicol. Vitro Int. J. Publ. Assoc. BIBRA. 2016;31:12–22.
Jones AL, Hulett MD, Parish CR. Histidine-rich glycoprotein: A novel adaptor protein in plasma that modulates the immune, vascular and coagulation systems. Immunol Cell Biol. 2005;83:106–18.
Jones AL, Hulett MD, Parish CR. Histidine-rich glycoprotein binds to cell-surface heparan sulfate via its N-terminal domain following Zn2+ chelation. J Biol Chem. 2004;279:30114–22.
Fedeli C, Segat D, Tavano R, Bubacco L, De Franceschi G, de Laureto PP, et al. The functional dissection of the plasma corona of SiO2-NPs spots histidine rich glycoprotein as a major player able to hamper nanoparticle capture by macrophages. Nanoscale. 2015;7:17710–28.
Ben-Arie N, Kedmi R, Peer D. Integrin-targeted nanoparticles for siRNA delivery. Methods Mol Biol Clifton NJ. 2012;757:497–507.
Sydlik U, Bierhals K, Soufi M, Abel J, Schins RPF, Unfried K. Ultrafine carbon particles induce apoptosis and proliferation in rat lung epithelial cells via specific signaling pathways both using EGF-R. Am. J. Physiol. Lung Cell. Mol. Physiol. 2006;291:L725–33.
Unfried K, Sydlik U, Bierhals K, Weissenberg A, Abel J. Carbon nanoparticle-induced lung epithelial cell proliferation is mediated by receptor-dependent Akt activation. Am J Physiol Lung Cell Mol Physiol. 2008;294:L358–67.
New DC, Wu K, Kwok AWS, Wong YH. G protein-coupled receptor-induced Akt activity in cellular proliferation and apoptosis. FEBS J. 2007;274:6025–36.
Singh RP, Ramarao P. Cellular uptake, intracellular trafficking and cytotoxicity of silver nanoparticles. Toxicol Lett. 2012;213:249–59.
Mustonen A-M, Nieminen P, Joukainen A, Jaroma A, Kääriäinen T, Kröger H, et al. First in vivo detection and characterization of hyaluronan-coated extracellular vesicles in human synovial fluid. J Orthop Res Off Publ Orthop Res Soc. 2016;34:1960–8.
Null NG, Gundogan B, Tan A, Farhatnia Y, Wu W, Rajadas J, et al. Exosomes as immunotheranostic nanoparticles. Clin Ther. 2014;36:820–9.
Zhu M, Tian X, Song X, Li Y, Tian Y, Zhao Y, et al. Nanoparticle-induced exosomes target antigen-presenting cells to initiate Th1-type immune activation. Small Weinh Bergstr Ger. 2012;8:2841–8.
Wang H, Wu L, Reinhard BM. Scavenger receptor mediated endocytosis of silver nanoparticles into J774A.1 macrophages is heterogeneous. ACS Nano. 2012;6:7122–32.
Hoppstädter J, Seif M, Dembek A, Cavelius C, Huwer H, Kraegeloh A, et al. M2 polarization enhances silica nanoparticle uptake by macrophages. Front Pharmacol. 2015;6:55.
Galili U. Acceleration of wound healing by α-gal nanoparticles interacting with the natural anti-Gal antibody. J Immunol Res. 2015;2015:589648.
Wigglesworth KM, Racki WJ, Mishra R, Szomolanyi-Tsuda E, Greiner DL, Galili U. Rapid recruitment and activation of macrophages by anti-Gal/α-Gal liposome interaction accelerates wound healing. J Immunol Baltim Md 1950. 2011;186:4422–32.
Kim M-S, Song HJ, Lee SH, Lee CK. Comparative study of various growth factors and cytokines on type I collagen and hyaluronan production in human dermal fibroblasts. J Cosmet Dermatol. 2014;13:44–51.
Vorstenbosch J, Gallant-Behm C, Trzeciak A, Roy S, Mustoe T, Philip A. Transgenic mice overexpressing CD109 in the epidermis display decreased inflammation and granulation tissue and improved collagen architecture during wound healing. Wound Repair Regen. Off. Publ. Wound Heal. Soc. Eur. Tissue Repair Soc. 2013;21:235–46.
Rangasamy S, Tak YK, Kim S, Paul A, Song JM. Bifunctional Therapeutic High-Valence Silver-Pyridoxine Nanoparticles with Proliferative and Antibacterial Wound-Healing Activities. J Biomed Nanotechnol. 2016;12:182–96.
Kwan KHL, Liu X, To MKT, Yeung KWK, Ho C, Wong KKY. Modulation of collagen alignment by silver nanoparticles results in better mechanical properties in wound healing. Nanomedicine Nanotechnol Biol Med. 2011;7:497–504.
Anderson DS, Patchin ES, Silva RM, Uyeminami DL, Sharmah A, Guo T, et al. Influence of particle size on persistence and clearance of aerosolized silver nanoparticles in the rat lung. Toxicol Sci Off J Soc Toxicol. 2015;144:366–81.
Lindroos PM, Coin PG, Badgett A, Morgan DL, Bonner JC. Alveolar macrophages stimulated with titanium dioxide, chrysotile asbestos, and residual oil fly ash upregulate the PDGF receptor-alpha on lung fibroblasts through an IL-1beta-dependent mechanism. Am J Respir Cell Mol Biol. 1997;16:283–92.
Richards CD. Innate Immune Cytokines, Fibroblast Phenotypes, and Regulation of Extracellular Matrix in Lung. J. Interferon Cytokine Res. Off. J. Int. Soc. Interferon Cytokine Res. 2017;37:52–61.
Brieland JK, Jones ML, Clarke SJ, Baker JB, Warren JS, Fantone JC. Effect of acute inflammatory lung injury on the expression of monocyte chemoattractant protein-1 (MCP-1) in rat pulmonary alveolar macrophages. Am J Respir Cell Mol Biol. 1992;7:134–9.
Liu H, Fang S, Wang W, Cheng Y, Zhang Y, Liao H, et al. Macrophage-derived MCPIP1 mediates silica-induced pulmonary fibrosis via autophagy. Part Fibre Toxicol. 2016;13:55.
Wan B, Wang Z-X, Lv Q-Y, Dong P-X, Zhao L-X, Yang Y, et al. Single-walled carbon nanotubes and graphene oxides induce autophagosome accumulation and lysosome impairment in primarily cultured murine peritoneal macrophages. Toxicol Lett. 2013;221:118–27.
Serra P, Bruczko M, Zapico JM, Puckowska A, Garcia MA, Martin-Santamaria S, et al. MMP-2 selectivity in hydroxamate-type inhibitors. Curr Med Chem. 2012;19:1036–64.
Supasorn O, Sringkarin N, Srimanote P, Angkasekwinai P. Matrix metalloproteinases contribute to the regulation of chemokine expression and pulmonary inflammation in Cryptococcus infection. Clin Exp Immunol. 2016;183:431–40.
Roulet A, Armand L, Dagouassat M, Rogerieux F, Simon-Deckers A, Belade E, et al. Intratracheally administered titanium dioxide or carbon black nanoparticles do not aggravate elastase-induced pulmonary emphysema in rats. BMC Pulm Med. 2012;12:38.
Bachoual R, Boczkowski J, Goven D, Amara N, Tabet L, On D, et al. Biological effects of particles from the paris subway system. Chem Res Toxicol. 2007;20:1426–33.
Hussain S, Boland S, Baeza-Squiban A, Hamel R, Thomassen LCJ, Martens JA, et al. Oxidative stress and proinflammatory effects of carbon black and titanium dioxide nanoparticles: role of particle surface area and internalized amount. Toxicology. 2009;260:142–9.
Lavigne MC, Eppihimer MJ. Cigarette smoke condensate induces MMP-12 gene expression in airway-like epithelia. Biochem Biophys Res Commun. 2005;330:194–203.
Fujita K, Horie M, Kato H, Endoh S, Suzuki M, Nakamura A, et al. Effects of ultrafine TiO2 particles on gene expression profile in human keratinocytes without illumination: involvement of extracellular matrix and cell adhesion. Toxicol Lett. 2009;191:109–17.
Poirier M, Simard J-C, Girard D. Silver nanoparticles of 70 nm and 20 nm affect differently the biology of human neutrophils. J Immunotoxicol. 2016;13:375–85.
Poirier M, Simard J-C, Antoine F, Girard D. Interaction between silver nanoparticles of 20 nm (AgNP20 ) and human neutrophils: induction of apoptosis and inhibition of de novo protein synthesis by AgNP20 aggregates. J Appl Toxicol JAT. 2014;34:404–12.
Bashur CA, Venkataraman L, Ramamurthi A. Tissue engineering and regenerative strategies to replicate biocomplexity of vascular elastic matrix assembly. Tissue Eng Part B Rev. 2012;18:203–17.
Armand L, Dagouassat M, Belade E, Simon-Deckers A, Le Gouvello S, Tharabat C, et al. Titanium dioxide nanoparticles induce matrix metalloprotease 1 in human pulmonary fibroblasts partly via an interleukin-1β-dependent mechanism. Am J Respir Cell Mol Biol. 2013;48:354–63.
Raymond L, Eck S, Mollmark J, Hays E, Tomek I, Kantor S, et al. Interleukin-1 beta induction of matrix metalloproteinase-1 transcription in chondrocytes requires ERK-dependent activation of CCAAT enhancer-binding protein-beta. J Cell Physiol. 2006;207:683–8.
Zhang X, Feng M, Liu X, Bai L, Kong M, Chen Y, et al. Persistence of cirrhosis is maintained by intrahepatic regulatory T cells that inhibit fibrosis resolution by regulating the balance of tissue inhibitors of metalloproteinases and matrix metalloproteinases. Transl Res J Lab Clin Med. 2016;169:67–79. e1-2
McHugh MD, Park J, Uhrich R, Gao W, Horwitz DA, Fahmy TM. Paracrine co-delivery of TGF-β and IL-2 using CD4-targeted nanoparticles for induction and maintenance of regulatory T cells. Biomaterials. 2015;59:172–81.
Kothapalli CR, Taylor PM, Smolenski RT, Yacoub MH, Ramamurthi A. Transforming growth factor beta 1 and hyaluronan oligomers synergistically enhance elastin matrix regeneration by vascular smooth muscle cells. Tissue Eng Part A. 2009;15:501–11.
Ma JY, Mercer RR, Barger M, Schwegler-Berry D, Scabilloni J, Ma JK, et al. Induction of pulmonary fibrosis by cerium oxide nanoparticles. Toxicol Appl Pharmacol. 2012;262:255–64.
Ma J, Mercer RR, Barger M, Schwegler-Berry D, Cohen JM, Demokritou P, et al. Effects of amorphous silica coating on cerium oxide nanoparticles induced pulmonary responses. Toxicol Appl Pharmacol. 2015;288:63–73.
Wight TN. Versican: a versatile extracellular matrix proteoglycan in cell biology. Curr Opin Cell Biol. 2002;14:617–23.
Brown-Augsburger P, Tisdale C, Broekelmann T, Sloan C, Mecham RP. Identification of an elastin cross-linking domain that joins three peptide chains. Possible role in nucleated assembly. J Biol Chem. 1995;270:17778–83.
Onoda M, Yoshimura K, Aoki H, Ikeda Y, Morikage N, Furutani A, et al. Lysyl oxidase resolves inflammation by reducing monocyte chemoattractant protein-1 in abdominal aortic aneurysm. Atherosclerosis. 2010;208:366–9.
Sylvester A, Sivaraman B, Deb P, Ramamurthi A. Nanoparticles for localized delivery of hyaluronan oligomers towards regenerative repair of elastic matrix. Acta Biomater. 2013;9:9292–302.
Joddar B, Ramamurthi A. Elastogenic effects of exogenous hyaluronan oligosaccharides on vascular smooth muscle cells. Biomaterials. 2006;27:5698–707.
Grossi C, Guccione C, Isacchi B, Bergonzi MC, Luccarini I, Casamenti F, Bilia AR. Development of Blood-Brain Barrier Permeable Nanoparticles as Potential Carriers for Salvianolic Acid B to CNS. Planta Med. 2017;83(5):382–391.
Bryant DM, Mostov KE. From cells to organs: building polarized tissue. Nat Rev Mol Cell Biol. 2008;9:887–901.
Bryant DM, Roignot J, Datta A, Overeem AW, Kim M, Yu W, et al. A molecular switch for the orientation of epithelial cell polarization. Dev Cell. 2014;31:171–87.
Strilić B, Kucera T, Eglinger J, Hughes MR, McNagny KM, Tsukita S, et al. The molecular basis of vascular lumen formation in the developing mouse aorta. Dev Cell. 2009;17:505–15.
Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P. Molecular Biology of the Cell. 4th ed. New York: Garland Science; 2002.
Kalluri R. Basement membranes: structure, assembly and role in tumour angiogenesis. Nat Rev Cancer. 2003;3:422–33.
Mehta D, Malik AB. Signaling mechanisms regulating endothelial permeability. Physiol Rev. 2006;86:279–367.
Li W, Szoka FC. Lipid-based nanoparticles for nucleic acid delivery. Pharm Res. 2007;24:438–49.
Landgraf L, Müller I, Ernst P, Schäfer M, Rosman C, Schick I, et al. Comparative evaluation of the impact on endothelial cells induced by different nanoparticle structures and functionalization. Beilstein J Nanotechnol. 2015;6:300–12.
Baldus S, Eiserich JP, Mani A, Castro L, Figueroa M, Chumley P, et al. Endothelial transcytosis of myeloperoxidase confers specificity to vascular ECM proteins as targets of tyrosine nitration. J Clin Invest. 2001;108:1759–70.
Nikitovic D, Holmgren A. S-nitrosoglutathione is cleaved by the thioredoxin system with liberation of glutathione and redox regulating nitric oxide. J Biol Chem. 1996;271:19180–5.
Lim SY, Raftery MJ, Goyette J, Geczy CL. S-glutathionylation regulates inflammatory activities of S100A9. J Biol Chem. 2010;285:14377–88.
Safar R, Ronzani C, Diab R, Chevrier J, Bensoussan D, Grandemange S, et al. Human monocyte response to S-nitrosoglutathione-loaded nanoparticles: uptake, viability, and transcriptome. Mol Pharm. 2015;12:554–61.
Treyer A, Müsch A. Hepatocyte polarity. Compr Physiol. 2013;3:243–87.
Prats-Mateu B, Ertl P, Toca-Herrera JL. Influence of HepG2 cell shape on nanoparticle uptake. Microsc Res Tech. 2014;77:560–5.
Jiménez Calvente C, Sehgal A, Popov Y, Kim YO, Zevallos V, Sahin U, et al. Specific hepatic delivery of procollagen α1(I) small interfering RNA in lipid-like nanoparticles resolves liver fibrosis. Hepatol Baltim Md. 2015;62:1285–97.
Medina SH, Tekumalla V, Chevliakov MV, Shewach DS, Ensminger WD, El-Sayed MEH. N-acetylgalactosamine-functionalized dendrimers as hepatic cancer cell-targeted carriers. Biomaterials. 2011;32:4118–29.
Availability of data and materials
This work is supported by the ERA.NET RUS Plus program (ID#169 - NABUCO), the Grant of Russian Science Foundation (15–14-20032) and COST Action TD1204 MODENA.
ABE; wrote the sections extracellular matrix – nanoparticles – aspects of immune interactions/considerations, membrane interactions and compiled the manuscript, DN; wrote the background and basic components of the extracellular matrix, MN; wrote the sections related to biological barriers, PHN; revised the manuscript, AOD; wrote the section related to nanoparticles-targeting, MIS; revised the manuscript, KG; revised the manuscript, AMT; designed the Project and edited the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Engin, A.B., Nikitovic, D., Neagu, M. et al. Mechanistic understanding of nanoparticles’ interactions with extracellular matrix: the cell and immune system. Part Fibre Toxicol 14, 22 (2017). https://doi.org/10.1186/s12989-017-0199-z
- Extracellular matrix
- Biological barriers