Age-dependent myocardial reinduction of apoptosis inhibitors under VAD in heart failure

被引:3
作者
Scheubel, RJ
Bartling, B
Stein, S
Darmer, D
Holtz, J
Pregla, R
Hetzer, R
Koerfer, R
Zerkowski, HR
Silber, RE
机构
[1] Univ Halle Wittenberg, Cardiovasc Surg Clin, D-06097 Halle Saale, Germany
[2] Univ Halle Wittenberg, Inst Pathophysiol, D-06097 Halle Saale, Germany
[3] Deutsch Herzzentrum, Berlin, Germany
[4] Ruhr Univ Bochum, Dept Thorac & Cardiovasc Surg, Heart & Diabet Ctr NRW, Bad Oeynhausen, Germany
[5] Univ Basel, Kantonsspital, Div Cardiothorac Surg, CH-4031 Basel, Switzerland
关键词
apoptosis; heart failure; ventricular assist device; gene expression; age dependence;
D O I
10.1055/s-2001-17798
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hemodynamic unloading using the ventricular assist device [VAD] results in partial functional recovery of failing hearts that show increased susceptibility to cardiomyocyte apoptosis. The caspase cascade is the central element of the apoptotic process in cells. We therefore tested expression shifts of left ventricular mRNA of caspases and their endogenous inhibitors from 15 patients with VAD support and successful bridging to transplantation using semiquantitative RT-PCR. Cardiac unloading was shown by the reduction in ventricular Pro-ANP mRNA under VAD. No alteration of mRNA expression under VAD could be observed for initiator caspases, for their selective inhibitors or for apoptotic signal molecules from the mitochondrial intermembrane space. Only two unselective cardiac IAPs (inhibitor of apoptosis protein) were increased under VAD with better recovery in younger patients. In conclusion, our findings indicate that successful hemodynamic unloading by VAD support causes only minor, age-dependent recovery in the expression of IAPs, while presumed alterations in antiapoptotic modulator systems upstream of the caspase cascade still remain to be identified.
引用
收藏
页码:268 / 272
页数:5
相关论文
共 21 条
[1]   Age-dependent expression of fibrosis-related genes and collagen deposition in the rat myocardium [J].
Annoni, G ;
Luvarà, G ;
Arosio, B ;
Gagliano, N ;
Fiordaliso, F ;
Santambrogio, D ;
Jeremic, G ;
Mircoli, L ;
Latini, R ;
Vergani, C ;
Masson, S .
MECHANISMS OF AGEING AND DEVELOPMENT, 1998, 101 (1-2) :57-72
[2]  
Bartling B, 1999, CIRCULATION, V100, P216
[3]   HYPOTHESIS - APOPTOSIS MAY BE A MECHANISM FOR THE TRANSITION TO HEART-FAILURE WITH CHRONIC PRESSURE-OVERLOAD [J].
BING, OHL .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1994, 26 (08) :943-948
[4]   Biochemical pathways of caspase activation during apoptosis [J].
Budihardjo, I ;
Oliver, H ;
Lutter, M ;
Luo, X ;
Wang, XD .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1999, 15 :269-290
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]   Left ventricular assist system support is associated with persistent inflammation and temporary immunosuppression [J].
Deng, MC ;
Erren, M ;
Tjan, TDT ;
Tamminga, N ;
Werntze, B ;
Zimmermann, P ;
Weyand, M ;
Hammel, D ;
Schmidt, C ;
Scheld, HH .
THORACIC AND CARDIOVASCULAR SURGEON, 1999, 47 :326-331
[7]   Mitochondria as the central control point of apoptosis [J].
Desagher, S ;
Martinou, JC .
TRENDS IN CELL BIOLOGY, 2000, 10 (09) :369-377
[8]   IAP family proteins - suppressors of apoptosis [J].
Deveraux, QL ;
Reed, TC .
GENES & DEVELOPMENT, 1999, 13 (03) :239-252
[9]   IMPROVED MORTALITY AND REHABILITATION OF TRANSPLANT CANDIDATES TREATED WITH A LONG-TERM IMPLANTABLE LEFT-VENTRICULAR ASSIST SYSTEM [J].
FRAZIER, OH ;
ROSE, EA ;
MCCARTHY, P ;
BURTON, NA ;
TECTOR, A ;
LEVIN, H ;
KAYNE, HL ;
POIRIER, VL ;
DASSE, KA .
ANNALS OF SURGERY, 1995, 222 (03) :327-338
[10]   Inhibition of death receptor signals by cellular FLIP [J].
Irmler, M ;
Thome, M ;
Hahne, M ;
Schneider, P ;
Hofmann, B ;
Steiner, V ;
Bodmer, JL ;
Schroter, M ;
Burns, K ;
Mattmann, C ;
Rimoldi, D ;
French, LE ;
Tschopp, J .
NATURE, 1997, 388 (6638) :190-195