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Table 1 Comparative summary of data from experiments using I.T. instillation (in vivo), I.V. injection (in vivo) and cultured endothelial cells (in vitro)

From: Platelet activation independent of pulmonary inflammation contributes to diesel exhaust particulate-induced promotion of arterial thrombosis

   

Particulate

  

Time (hours)

DEP

CB

DQ12

I.T. instillation

Pulmonary cells

2

NSD

------

------

(In vivo)

 

6

↑

↑↑

↑↑

  

24

NSD

------

------

 

Pulmonary IL-6

6

↑

↑

NSD

 

Pulmonary TNFα

6

NSD

NSD

NSD

 

Pulmonary CRP

6

NSD

↑↑

↑↑

 

Plasma IL-6

6

NSD

NSD

NSD

 

Plasma TNFα

6

NSD

NSD

NSD

 

Plasma CRP

6

NSD

↑↑

↑↑

 

Thrombosis

2

NSD

------

------

  

6

↑

NSD

NSD

  

24

NSD

------

------

 

tPA:PAI-1

6

↓↓

↓↓

↓↓

 

PMA

 

↑↑

NSD

NSD

I.V. injection

Pulmonary cells

2

NSD

------

------

(In vivo)

 

6

NSD

NSD

------

  

24

NSD

------

------

 

Pulmonary IL-6

2

L.O.D

L.O.D.

------

 

Pulmonary TNFα

2

NSD

NSD

------

 

Pulmonary CRP

2

NSD

NSD

------

 

Plasma IL-6

2

NSD

NSD

------

 

Plasma TNFα

2

NSD

NSD

------

 

Plasma CRP

2

NSD

↑↑

------

 

Thrombosis

2

↑

------

------

  

6

NSD

NSD

------

  

24

NSD

------

------

 

tPA:PAI-1

6

↓↓

↓↓

------

 

PMA

24

↑

NSD

------

Cultured HUVECs

tPA transcripts

Basal

↓

------

------

In vitro

 

Stimulated

NSD

------

------

 

PAI-1 transcripts

Basal

NSD

------

------

  

Stimulated

↓

------

------

 

tPA antigen

6

NSD

------

------

  

24

↓↓

------

------

 

PAI-1 activity

6

↓↓

------

------

  

24

↓↓

------

------

  1. CB carbon black, CRP C-reactive protein, DEP diesel exhaust particles, DQ12 quartz particles, HUVEC human umbilical vein endothelial cells, IL-6 interleukin 6, PAI-1 plasminogen activator inhibitor, PMA platelet monocyte aggregation, TNFα tumour necrosis factor-α, tPA tissue plasminogen activator
  2. NSD = no significant difference. ----- = not tested (note, DQ12 was not tested by iv injection or cultured endothelial cells as this particle is unlikely to cross from the lungs into the circulation due to its micrometre size)