C-reactive protein upregulates complement-inhibitory factors in endothelial cells.

Abstract:

BACKGROUND:Because complement-mediated vascular injury participates in atherosclerosis and C-reactive protein (CRP) can activate the complement cascade, we sought to determine whether CRP affects the expression of the protective complement-inhibitory factors on the cell surface of endothelial cells (ECs). METHODS AND RESULTS:Human coronary artery or human saphenous vein ECs were incubated with CRP (0 to 100 microg/mL, 0 to 72 hours), and the expression of the complement-inhibitory proteins decay-accelerating factor (DAF), membrane cofactor protein (CD46), and CD59 were measured by flow cytometry. Incubation with CRP resulted in a significant increase in the expression of all 3 proteins. CRP-induced upregulation of DAF required increased steady-state mRNA and de novo protein synthesis. The increased expression of complement-inhibitory proteins was functionally effective, resulting in significant reduction of complement-mediated lysis of antibody-coated human saphenous vein ECs. CONCLUSIONS:These observations provide evidence for a possible protective role for CRP in atherogenesis.

journal_name

Circulation

journal_title

Circulation

authors

Li SH,Szmitko PE,Weisel RD,Wang CH,Fedak PW,Li RK,Mickle DA,Verma S

doi

10.1161/01.CIR.0000117087.27524.0E

subject

Has Abstract

pub_date

2004-02-24 00:00:00

pages

833-6

issue

7

eissn

0009-7322

issn

1524-4539

pii

01.CIR.0000117087.27524.0E

journal_volume

109

pub_type

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