器官移植中受调控的细胞死亡:最新进展和机制综述。

IF 5.9 2区 生物学 Q2 CELL BIOLOGY
Qian Chen, Jiashi Sun, Shifan Zhu, Minghui Wu, Hakjun Lee, Azeem Alam, Moradi Kimia, Enqiang Chang, Hailin Zhao, Yue Jin, Daqing Ma
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引用次数: 0

摘要

器官移植是终末期器官功能障碍和衰竭患者的最终治疗选择。缺血再灌注(IR)损伤是移植物利用率低的主要原因之一,因为它显著增加了移植物原发性功能障碍和移植后急性排斥反应的风险。与脑死亡(DBD)供者相比,从循环死亡(DCD)供者获得的器官的这种风险尤其高。IR损伤通过多种机制加剧组织损伤,包括诱导受调节的细胞死亡。受调控的细胞死亡及其后果在决定移植物存活和功能方面起着关键作用,从而影响移植的整体成功。了解IR损伤中受调控细胞死亡的机制对于制定治疗策略以减少组织损伤和改善器官移植的临床结果至关重要。本文主要讨论了临床前DBD和DCD器官移植中不同类型的受调控细胞死亡以及预防细胞死亡策略的潜在机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulated cell death in organ transplantation: Recent developments and mechanistic overview.

Organ transplantation is a definitive therapeutic option for patients with end-stage organ dysfunction and failure. Ischaemia-reperfusion (IR) injury is one of the leading causes of low graft utilisation as it significantly increases the risk of primary graft dysfunction and acute rejection following transplantation. This risk is particularly high for organs obtained from donors after circulatory death (DCD) when compared with the donors from brain death (DBD). IR injury exacerbates tissue damage via various mechanisms including the induction of regulated cell death. Regulated cell death and its consequences play critical roles in determining graft survival and function, thereby influencing the overall success of the transplant. Understanding the mechanisms underlying regulated cell death in IR injury is essential for developing therapeutic strategies to minimise tissue damage and improve clinical outcomes in organ transplantation. This review mainly discussed different types of regulated cell death and underlying mechanisms towards preventive cell death strategies in DBD and DCD organ transplantation in preclinical settings.

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来源期刊
CiteScore
9.60
自引率
1.80%
发文量
1383
期刊介绍: The Journal of Molecular Cell Biology ( JMCB ) is a full open access, peer-reviewed online journal interested in inter-disciplinary studies at the cross-sections between molecular and cell biology as well as other disciplines of life sciences. The broad scope of JMCB reflects the merging of these life science disciplines such as stem cell research, signaling, genetics, epigenetics, genomics, development, immunology, cancer biology, molecular pathogenesis, neuroscience, and systems biology. The journal will publish primary research papers with findings of unusual significance and broad scientific interest. Review articles, letters and commentary on timely issues are also welcome. JMCB features an outstanding Editorial Board, which will serve as scientific advisors to the journal and provide strategic guidance for the development of the journal. By selecting only the best papers for publication, JMCB will provide a first rate publishing forum for scientists all over the world.
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