生死边缘的细胞:自噬与凋亡的串扰。

Daniela Kasprowska-Liśkiewicz
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引用次数: 60

摘要

近年来,自噬与细胞凋亡之间的相互作用引起了广泛的关注。基础自噬有助于维持细胞稳态,而这一过程的上调是应激反应的一个要素,使细胞能够在不利条件下生存。自噬也可能通过与细胞死亡途径的相互作用决定细胞的命运。控制这两个过程的起始和执行阶段的蛋白质网络是高度互联的。关于自噬和细胞凋亡之间的相互作用存在几种可能的解释。在大多数情况下,自噬的激活代表了细胞应对应激的一种尝试,并保护细胞免于凋亡或延迟其启动。一般来说,促生存和促死亡途径的同时激活被自噬和凋亡之间的相互抑制串扰所阻止。但在某些情况下,自噬或核心自噬机制的蛋白质可能通过过度的自我消化(所谓的“自噬细胞死亡”)或通过刺激其他细胞死亡途径的激活来促进细胞死亡。细胞是否真的通过自噬死亡是有争议的,这就是为什么“自噬细胞死亡”这一术语最近引起了激烈的争论。本文综述了近年来自噬与细胞凋亡之间的多水平串扰,从共同调控因子、相互抑制、自噬或自噬蛋白对细胞凋亡的刺激以及自噬在死亡-执行机制中的作用等方面进行了综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The cell on the edge of life and death: Crosstalk between autophagy and apoptosis.

Recently, the crosstalk between autophagy and apoptosis has attracted broader attention. Basal autophagy serves to maintain cell homeostasis, while the upregulation of this process is an element of stress response that enables the cell to survive under adverse conditions. Autophagy may also determine the fate of the cell through its interactions with cell death pathways. The protein networks that control the initiation and the execution phase of these two processes are highly interconnected. Several scenarios for the crosstalk between autophagy and apoptosis exist. In most cases, the activation of autophagy represents an attempt of the cell to cope with stress, and protects the cell from apoptosis or delays its initiation. Generally, the simultaneous activation of pro-survival and pro-death pathways is prevented by the mutual inhibitory crosstalk between autophagy and apoptosis. But in some circumstances, autophagy or the proteins of the core autophagic machinery may promote cellular demise through excessive self-digestion (so-called "autophagic cell death") or by stimulating the activation of other cell death pathways. It is controversial whether cells actually die via autophagy, which is why the term "autophagic cell death" has been under intense debate lately. This review summarizes the recent findings on the multilevel crosstalk between autophagy and apoptosis in aspects of common regulators, mutual inhibition of these processes, the stimulation of apoptosis by autophagy or autophagic proteins and finally the role of autophagy as a death-execution mechanism.

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