Molecular markers of programmed cell death in donor hearts before transplantation

被引:15
作者
Marasco, Silvana F. [1 ,2 ]
Sheeran, Freya L. [3 ,4 ]
Chaudhuri, Krishanu [1 ,2 ]
Vale, Matthew [1 ]
Bailey, Michael [5 ]
Pepe, Salvatore [2 ,3 ,4 ]
机构
[1] Alfred Hosp, Cardiothorac Surg Unit, Melbourne, Vic, Australia
[2] Monash Univ, Dept Surg, Melbourne, Vic 3004, Australia
[3] Univ Melbourne, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[4] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
[5] Monash Univ, Dept Epidemiol & Prevent Med, Melbourne, Vic 3004, Australia
关键词
heart transplantation; donor heart; donation after circulatory death; apoptosis; primary graft failure; HYPOXIA-INDUCED APOPTOSIS; MYOCARDIAL-ISCHEMIA; DNA-DAMAGE; HIF-1-ALPHA; DYSFUNCTION; ACTIVATION; FAILURE; SURGERY; PROTEIN; IMPACT;
D O I
10.1016/j.healun.2013.10.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: In this study we investigate whether pro-apoptotic, pro-inflammatory and other early signaling markers indicative of increased propensity for cell death processes were evident in human donor heart allografts immediately before transplantation, and whether there is an association with primary graft failure. METHODS: A prospective study was performed utilizing donor left atrial myocardium collected at the time of implantation of hearts from brain-dead donors (BDD, n = 29). In addition, to explore the potential of donor hearts from donation after circulatory death (DCD), myocardial samples were obtained during transplantation of lungs from DCD donors (n = 6). A comparator reference group (n = 7) consisted of left atrial specimens from patients undergoing mitral valve surgery. RESULTS: Significantly raised levels of caspase-3 specific activity, activated hypoxia inducible factor-1 (HIP-1 alpha) and 8-hydroxy-2'-deoxyguanosine were evident in the transplanted hearts (from BDD) that developed primary graft failure (n = 11). DCD hearts did not differ from BDD with regard to mRNA expression levels of FAS, Box, IL-6 and caspase-3. Although DCD hearts exhibited lower caspase-3 specific activity and activated hypoxia-inducible factor-1 protein, they had higher levels of mRNA for NF-kappa B, Bnip3 and caspase-1 mRNA. Increased 8-hydroxy-2'-deoxyguanosine levels reflected greater oxidative stress and reactive oxygen species-related DNA fragmentation. CONCLUSIONS: Our data indicate a significant role of pro-apoptotic and pro-inflammatory activity in allografts that subsequently exhibit primary graft failure. The relatively lower levels of apoptotic and inflammatory activity in DCD hearts suggest they may represent a potentially usable donor cardiac allograft pool. This possibility requires further detailed molecular and clinical research. Crown Copyright (C) 2014 Published by Elsevier Inc. on behalf of International Society for Heart and Lung Transplantation. All rights reserved.
引用
收藏
页码:185 / 193
页数:9
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