TNF-related apoptosis-inducing ligand and its decoy receptor osteoprotegerin in nonischemic dilated cardiomyopathy

被引:27
作者
Schoppet, M [1 ]
Ruppert, V
Hofbauer, LC
Henser, S
Al-Fakhri, N
Christ, M
Pankuweit, S
Maisch, B
机构
[1] Univ Marburg, Dept Internal Med & Cardiol, D-35033 Marburg, Germany
[2] Univ Marburg, Dept Internal Med & Gastroenterol & Endocrinol, D-35033 Marburg, Germany
[3] Univ Marburg, Dept Clin Chem, D-35033 Marburg, Germany
关键词
apoptosis; dilated cardiomyopathy; heart failure; osteoprotegerin; TRAIL;
D O I
10.1016/j.bbrc.2005.10.136
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptosis has been attributed an essential role in dilated cardiomyopathy (DCM) recently. We assessed expression of TNF-related apoptosis-inducing ligand (TRAIL) and its decoy receptor osteoprotegerin (OPG) in men with nonischemic DCM, who underwent coronary angiography and endomyocardial biopsy (EMB) after exclusion of coronary artery disease compared to control patients. TRAIL plasma concentrations were elevated in DCM (p = 0.02 vs. controls), and were positively correlated with left ventricular enddiastolic diameter (r = 0.15, p = 0.04), whereas OPG plasma levels did not differ between both groups (p = 0.96). In EMB of DCM patients, TRAIL and OPG protein were detected by immunohistochemistry but not in controls. Furthermore, gene expression in EMB or peripheral blood leukocytes (PBL) of DCM patients assessed by real-time PCR showed an increase of TRAIL mRNA in PBL (p = 0.01 vs. controls), whereas OPG mRNA was upregulated in endomyocardial specimens (p < 0.001 vs. controls). In conclusion, myocardial overexpression of antiapoptotic OPG in DCM patients may represent a compensatory mechanism to limit systemic activation of TRAIL in patients with congestive heart disease. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1745 / 1750
页数:6
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