Cardiomyocyte death in patients with end-stage heart failure before and after support with a left ventricular assist device: Low incidence of apoptosis despite ubiquitous mediators

被引:28
作者
de Jonge, N
van Wichen, DF
van Kuik, J
Kirkels, H
Lahpor, JR
Gmelig-Meyling, FHJ
van den Tweel, JG
de Weger, RA
机构
[1] Univ Utrecht, Med Ctr, Heart Failure & Heart Transplantat Unit, Heart Lung Ctr Utrecht, NL-3508 GA Utrecht, Netherlands
[2] Univ Utrecht, Med Ctr, Dept Pathol, Utrecht, Netherlands
[3] Univ Utrecht, Med Ctr, Dept Immunol, Utrecht, Netherlands
关键词
D O I
10.1016/S1053-2498(02)01160-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Left ventricular assist device (LVAD) implantation in patients with end-stage heart failure results in impressive hemodynamic improvement. The effects on myocardial apoptosis and its mediators are unknown. Methods: Myocardial biopsies from 17 patients at the time of LVAD implantation and after explantation, at the time of heart transplantation (HTx), were examined by terminal deoxynucleotidyltransferase-mediated dUTP nick-end labeling (TUNEL) reaction and with antibodies against Fas ligand (FasL), Fas, tumor necrosis factor (TNF)-alpha receptor 1 (TNF-R1), TNF-alpha receptor 2 (TNF-R2), TNF-alpha, TNF-alpha-converting enzyme (TACE), poly(ADP-ribose) polymerase (PARP), poly(ADPribose) (PAR), caspase-3 and FLICE inhibitory protein (FLIP). Results: Apoptosis incidence was low: 0.8% (range 0% to. 3%) positive cardiomyocytes nuclei before support, and 0.1% (range 0% to 0.6%) after support (p < 0.01). This was accompanied by low expression of caspase-3 and high expression of the. DNA repair enzyme, PARP. Its product, PAR, increased after support. Mediators and receptors inducing apoptosis as well as FLIP were widely present before and after support. Conclusions: Despite the abundant presence of mediators and receptors inducing apoptosis, the incidence of apoptosis itself was low before and after mechanical support. The abundant expression of FLIP may suggest an important role for this protein in the inhibition of cardiomyocyte death.
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页码:1028 / 1036
页数:9
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