Expression of CD40 in vascular smooth muscle cells and macrophages is associated with early development of human atherosclerotic lesions

被引:71
作者
Bruemmer, D
Riggers, U
Holzmeister, J
Grill, M
Lippek, F
Settmacher, U
Regitz-Zagrosek, V
Fleck, E
Graf, K
机构
[1] Deutsch Herzzentrum Berlin, D-13353 Berlin, Germany
[2] Dept Med Cardiol, Berlin, Germany
[3] Dept Pathol, Berlin, Germany
[4] Dept Surg, Charite, Berlin, Germany
关键词
D O I
10.1016/S0002-9149(00)01266-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CD40-CD154-mediated signaling has recently been described as playing a role in cellular functions involved in atherosclerotic processes. CD40 is expressed in macrophages, lymphocytes, endothelial cells, and vascular smooth muscle cells. However, cross-sectional studies investigating the expression of CD40 in atherosclerotic lesions are lacking. In the present study the expression of CD40 was studied in atherosclerotic lesions from 43 patients classified according to the World Health Organization criteria. Serial immunohistologic stainings of human iliac arteries from 43 patients were performed using monoclonal antibodies. Lesions were classified according to World Health Organization criteria, and CD40 expression was analyzed with regard to cell morphology and cellular markers by 2 independent observers. Human atherosclerotic lesions revealed a significant increase in intimal thickness, number of inflammatory infiltrates, and CD40-positive macrophages and vascular smooth muscle cells with progression of the lesions. This increase was most prominent from stage 0 to stage 1. A significant correlation between intimal thickness and CD40-positive macrophages (r = 0.75, p <0.0005) and CD40-positive vascular smooth muscle cells (r = 0.81, p <0.0005) was observed. Ligation of the cellular CD40 receptor contributes to inflammatory cellular events in human vascular smooth muscle cells. These data suggest a direct association of CD40 expression in atherosclerotic lesions with early plaque development. (C) 2001 by Excerpta Medico, Inc.
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页码:21 / 27
页数:7
相关论文
共 22 条
[1]   Enhanced levels of soluble and membrane-bound CD40 ligand in patients with unstable angina -: Possible reflection of T lymphocyte and platelet involvement in the pathogenesis of acute coronary syndromes [J].
Aukrust, P ;
Müller, F ;
Ueland, T ;
Berget, T ;
Aaser, E ;
Brunsvig, A ;
Solum, NO ;
Forfang, K ;
Froland, SS ;
Gullestad, L .
CIRCULATION, 1999, 100 (06) :614-620
[2]   Leucocyte recruitment in rupture prone regions of lipid-rich plaques: a prominent role for neovascularization? [J].
de Boer, OJ ;
van der Wal, AC ;
Teeling, P ;
Becker, AE .
CARDIOVASCULAR RESEARCH, 1999, 41 (02) :443-449
[3]   CD40 ligand on activated platelets triggers an inflammatory reaction of endothelial cells [J].
Henn, V ;
Slupsky, JR ;
Gräfe, M ;
Anagnostopoulos, I ;
Förster, R ;
Müller-Berghaus, G ;
Kroczek, RA .
NATURE, 1998, 391 (6667) :591-594
[4]   EXPRESSION OF FUNCTIONAL CD40 BY VASCULAR ENDOTHELIAL-CELLS [J].
HOLLENBAUGH, D ;
MISCHELPETTY, N ;
EDWARDS, CP ;
SIMON, JC ;
DENFELD, RW ;
KEINER, PA ;
ARUFFO, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (01) :33-40
[5]   CD40 ON HUMAN ENDOTHELIAL-CELLS - INDUCIBILITY BY CYTOKINES AND FUNCTIONAL REGULATION OF ADHESION MOLECULE EXPRESSION [J].
KARMANN, K ;
HUGHES, CCW ;
SCHECHNER, J ;
FANSLOW, WC ;
POBER, JS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (10) :4342-4346
[6]  
KIENER PA, 1995, J IMMUNOL, V155, P4917
[7]   Cytokine-inducible CD40 gene expression in vascular smooth muscle cells is mediated by nuclear factor κB and signal transducer and activate of transcription-1 [J].
Krzesz, R ;
Wagner, AH ;
Cattaruzza, M ;
Hecker, M .
FEBS LETTERS, 1999, 453 (1-2) :191-196
[8]   CD40-CD40L interactions in atherosclerosis [J].
Laman, JD ;
deSmet, BJGL ;
Schoneveld, A ;
vanMeurs, M .
IMMUNOLOGY TODAY, 1997, 18 (06) :272-277
[9]  
LAUTSCH EV, 1953, LAB INVEST, V2, P397
[10]   CD40L activation in circulating platelets in patients with acute coronary syndrome [J].
Lee, Y ;
Lee, WH ;
Lee, SC ;
Ahn, KJ ;
Choi, YH ;
Park, SW ;
Lee, SH ;
Seo, JD ;
Park, JE .
CARDIOLOGY, 1999, 92 (01) :11-16