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设计性死亡:细胞凋亡、坏死与自噬

Death by design: apoptosis, necrosis and autophagy.

作者信息

Edinger Aimee L, Thompson Craig B

机构信息

University of Pennsylvania, Abramson Family Cancer Research Institute, 450 BRB II/III, 421 Curie Blvd, Philadelphia, Pennsylvania 19104, USA.

出版信息

Curr Opin Cell Biol. 2004 Dec;16(6):663-9. doi: 10.1016/j.ceb.2004.09.011.

Abstract

Apoptosis is the principal mechanism by which cells are physiologically eliminated in metazoan organisms. During apoptotic death, cells are neatly carved up by caspases and packaged into apoptotic bodies as a mechanism to avoid immune activation. Recently, necrosis, once thought of as simply a passive, unorganized way to die, has emerged as an alternate form of programmed cell death whose activation might have important biological consequences, including the induction of an inflammatory response. Autophagy has also been suggested as a possible mechanism for non-apoptotic death despite evidence from many species that autophagy represents a survival strategy in times of stress. Recent advances have helped to define the function of and mechanism for programmed necrosis and the role of autophagy in cell survival and suicide.

摘要

细胞凋亡是后生动物体内细胞进行生理性清除的主要机制。在凋亡性死亡过程中,细胞被半胱天冬酶精确切割,并包装成凋亡小体,以此作为避免免疫激活的一种机制。最近,坏死,曾被认为仅仅是一种被动、无组织的死亡方式,现已成为程序性细胞死亡的另一种形式,其激活可能会产生重要的生物学后果,包括引发炎症反应。尽管许多物种的证据表明自噬是应激状态下的一种生存策略,但自噬也被认为是一种可能的非凋亡性死亡机制。最近的进展有助于明确程序性坏死的功能和机制,以及自噬在细胞存活和自杀中的作用。

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