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生死平衡——自噬与细胞凋亡相互作用的机制观点。

Life in the balance - a mechanistic view of the crosstalk between autophagy and apoptosis.

机构信息

Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, 76100 Israel.

出版信息

J Cell Sci. 2012 Nov 15;125(Pt 22):5259-68. doi: 10.1242/jcs.115865.

Abstract

Cellular stress triggers a fascinating decision-making process in cells; they can either attempt to survive until the stress is resolved through the activation of cytoprotective pathways, such as autophagy, or can commit suicide by apoptosis in order to prevent further damage to surrounding healthy cells. Although autophagy and apoptosis constitute distinct cellular processes with often opposing outcomes, their signalling pathways are extensively interconnected through various mechanisms of crosstalk. The physiological relevance of the autophagy-apoptosis crosstalk is not well understood, but it is presumed to facilitate a controlled and well-balanced cellular response to a given stress signal. In this Commentary, we explore the various mechanisms by which autophagy and apoptosis regulate each other, and define general paradigms of crosstalk on the basis of mechanistic features. One paradigm relates to physical and functional interactions between pairs of specific apoptotic and autophagic proteins. In a second mechanistic paradigm, the apoptosis or autophagy processes (as opposed to individual proteins) regulate each other through induced caspase and autolysosomal activity, respectively. In a third paradigm unique to autophagy, caspases are recruited and activated on autophagosomal membranes. These mechanistic paradigms are discernible experimentally, and can therefore be used as a practical guide for the interpretation of experimental data.

摘要

细胞应激会触发细胞内一个引人入胜的决策过程;它们可以通过激活细胞保护途径(如自噬)来尝试在应激得到解决之前存活下来,或者通过细胞凋亡来自杀,以防止周围健康细胞受到进一步的损伤。尽管自噬和细胞凋亡构成了具有相反结果的不同细胞过程,但它们的信号通路通过各种串扰机制广泛相互关联。自噬-细胞凋亡串扰的生理相关性尚不清楚,但据推测,它有助于对特定应激信号进行受控和平衡的细胞反应。在这篇评论中,我们探讨了自噬和细胞凋亡相互调节的各种机制,并根据机制特征定义了串扰的一般范例。一个范例涉及特定凋亡和自噬蛋白对之间的物理和功能相互作用。在第二个机制范例中,凋亡或自噬过程(而不是单个蛋白)通过诱导的半胱天冬酶和自噬溶酶体活性分别调节彼此。在自噬特有的第三个范例中,半胱天冬酶被募集并在自噬小体膜上激活。这些机制范例在实验中是可辨别的,因此可以作为解释实验数据的实用指南。

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