CD40-CD154 expression in calcified and non-calcified coronary lesions of patients with chronic renal failure

被引:27
作者
Campean, Valentina
Neureiter, Daniel
Nonnast-Daniel, Barbara
Garlichs, Christoph
Gross, Marie-Luise
Amann, Kerstin
机构
[1] Univ Erlangen Nurnberg, Dept Pathol, D-91054 Erlangen, Germany
[2] Dept Pathol, Heidelberg, Germany
关键词
atherosclerosis; chronic kidney disease; CD40; CD154; inflammation;
D O I
10.1016/j.atherosclerosis.2006.01.014
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
The high incidence of cardiovascular complications in patients with chronic renal failure (CRF) is partly explained by more aggressive atherosclerosis, i.e. increased incidence and severity of lesions with higher tendency to calcification. The pathogenesis of this accelerated atherosclerosis, however, is not completely understood. Among other risk factors, chronic micro-inflammation may be involved. Activation of cells and adhesion molecules in atherosclerosis is governed by CD40-CD154 (CD40 ligand) interaction. Therefore, we investigated the expression and distribution of CD40-CD154 in different coronary atherosclerotic lesions of CRF patients and non-renal control patients. Coronary plaques of 57 patients with and without CRF were categorized according to the Stary classification and analysed for in situ protein expression of CD40, CD154 and CRP using immunohistochemistry and a semiquantitative scoring system. The nature, number and distribution of infiltrating cells was analysed and correlated to the types of coronary lesions and in particular to the presence of calcification. CD40 was over expressed in media myocytes of coronary plaques of both uremic and control patients. Inside the plaques, CD40 was expressed on endothelial cells, T lymphocytes, macrophages, fibroblasts, and smooth muscle cells. CD 154 expression was seen on T cells in areas densely infiltrated by CD40 positive macrophages. In uremic and control patients higher in situ expression of CD40, CD154 and CRP was seen in calcified compared to non-calcified lesions. Inside the plaques, there were significant differences in the expression pattern of CD40 and CD154 between uremic and control patients. In addition, in uremic patients coronary plaques showed higher CRP protein expression compared to control patients. The data indicate a higher inflammatory status of coronary lesions as well as involvement of the CD40-CD154 signaling cascade in CRF patients, especially in cases of calcified atherosclerotic lesions. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:156 / 166
页数:11
相关论文
共 51 条
[1]
Induction of tissue factor expression in human endothelial cells by CD40 ligand is mediated via activator protein 1, nuclear factor κB, and Egr-1 [J].
Bavendiek, U ;
Libby, P ;
Kilbride, M ;
Reynolds, R ;
Mackman, N ;
Schönbeck, U .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (28) :25032-25039
[2]
Influence of age and end-stage renal disease on the stiffness of carotid wall material in hypertension [J].
Blacher, J ;
London, GM ;
Safar, ME ;
Mourad, JJ .
JOURNAL OF HYPERTENSION, 1999, 17 (02) :237-244
[3]
Association of serum phosphorus and calcium x phosphate product with mortality risk in chronic hemodialysis patients: A national study [J].
Block, GA ;
Hulbert-Shearon, TE ;
Levin, NW ;
Port, FK .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 31 (04) :607-617
[4]
Electron beam computed tomography in the evaluation of cardiac calcifications in chronic dialysis patients [J].
Braun, J ;
Oldendorf, M ;
Moshage, W ;
Heidler, R ;
Zeitler, E ;
Luft, FC .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1996, 27 (03) :394-401
[5]
Expression of CD40 in vascular smooth muscle cells and macrophages is associated with early development of human atherosclerotic lesions [J].
Bruemmer, D ;
Riggers, U ;
Holzmeister, J ;
Grill, M ;
Lippek, F ;
Settmacher, U ;
Regitz-Zagrosek, V ;
Fleck, E ;
Graf, K .
AMERICAN JOURNAL OF CARDIOLOGY, 2001, 87 (01) :21-27
[6]
CD40 ligand is selectively expressed on CD4+ T cells and platelets:: implications for CD40-CD40L signalling in atherosclerosis [J].
Büchner, K ;
Henn, V ;
Gräfe, M ;
de Boer, OJ ;
Becker, AE ;
Kroczek, RA .
JOURNAL OF PATHOLOGY, 2003, 201 (02) :288-295
[7]
The apolipoprotein E knockout mouse:: A model documenting accelerated atherogenesis in uremia [J].
Buzello, M ;
Törnig, J ;
Faulhaber, J ;
Ehmke, H ;
Ritz, E ;
Amann, K .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (02) :311-316
[8]
Determinants of progressive vascular calcification in haemodialysis patients [J].
Chertow, GM ;
Raggi, P ;
Chasan-Taber, S ;
Bommer, J ;
Holzer, H ;
Burke, SK .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2004, 19 (06) :1489-1496
[9]
NF-κB:: pivotal mediator or innocent bystander in atherogenesis? [J].
Collins, T ;
Cybulsky, MI .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (03) :255-264
[10]
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