Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
Sir William Dunn School of Pathology, University of Oxford, UK.
FEBS J. 2021 Apr;288(7):2166-2183. doi: 10.1111/febs.15547. Epub 2020 Sep 21.
Apoptosis is a major form of programmed cell death (PCD) that eliminates unnecessary and potentially dangerous cells in all metazoan organisms, thus ensuring tissue homeostasis and many developmental processes. Accordingly, defects in the activation of the apoptotic pathway often pave the way to disease. After several decades of intensive research, the molecular details controlling the apoptosis program have largely been unraveled, as well as the regulatory mechanisms of caspase activation during apoptosis. Nevertheless, an ever-growing list of studies is suggesting the essential role of caspases and other apoptotic proteins in ensuring nonlethal cellular functions during normal development, tissue repair, and regeneration. Moreover, if deregulated, these novel nonapoptotic functions can also instigate diseases. The difficulty of identifying and manipulating the caspase-dependent nonlethal cellular processes (CDPs), as well as the nonlethal functions of other cell death proteins (NLF-CDPs), meant that CDPs and NLF-CDPs have been only curiosities within the apoptotic field; however, the recent technical advancements and the latest biological findings are assigning an unanticipated biological significance to these nonapoptotic functions. Here, we summarize the various talks presented in the first international conference fully dedicated to discuss CDPs and NFL-CDPs and named 'The Batsheva de Rothschild Seminar on Non-Apoptotic Roles of Apoptotic Proteins'. The conference was organized between September 22, 2019, and 25, 2019, by Eli Arama (Weizmann Institute of Science), Luis Alberto Baena-Lopez (University of Oxford), and Howard O. Fearnhead (NUI Galway) at the Weizmann Institute of Science in Israel, and hosted a large international group of researchers.
细胞凋亡是一种主要的程序性细胞死亡(PCD)形式,它可以消除所有后生动物组织中不必要和潜在危险的细胞,从而确保组织的内稳态和许多发育过程。因此,凋亡途径激活缺陷常常导致疾病的发生。经过几十年的深入研究,控制凋亡程序的分子细节以及凋亡过程中半胱天冬酶激活的调节机制已经被很大程度地揭示出来。然而,越来越多的研究表明,半胱天冬酶和其他凋亡蛋白在确保正常发育、组织修复和再生过程中非致死性细胞功能中的重要作用。此外,如果这些蛋白的功能失调,它们的这些新的非凋亡性功能也可以引发疾病。由于难以识别和操纵依赖半胱天冬酶的非致死性细胞过程(CDPs)以及其他细胞死亡蛋白的非致死性功能(NLF-CDPs),这些 CDPs 和 NLF-CDPs 一直是凋亡领域的研究热点;然而,最近的技术进步和最新的生物学发现赋予了这些非凋亡性功能意想不到的生物学意义。在这里,我们总结了第一届专门讨论 CDPs 和 NFL-CDPs 的国际会议上的各种报告,该会议被命名为“巴氏德罗斯柴尔德关于凋亡蛋白非凋亡作用研讨会”。该会议于 2019 年 9 月 22 日至 25 日在以色列魏茨曼科学研究所由 Eli Arama(魏茨曼科学研究所)、Luis Alberto Baena-Lopez(牛津大学)和 Howard O. Fearnhead(戈尔韦国立大学)组织,会议邀请了一大批国际研究人员参加。