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Bcl-2 蛋白对非典型细胞命运的调控。

Noncanonical Cell Fate Regulation by Bcl-2 Proteins.

机构信息

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

Department of Clinical and Molecular Sciences, Marche Polytechnic University, Ancona, Italy.

出版信息

Trends Cell Biol. 2020 Jul;30(7):537-555. doi: 10.1016/j.tcb.2020.03.004. Epub 2020 Apr 16.

Abstract

Bcl-2 proteins are widely known as key controllers of mitochondrial outer membrane permeabilization, arguably the most important step of intrinsic apoptosis. Accumulating evidence indicate that most, if not all, members of the Bcl-2 protein family also mediate a number of apoptosis-unrelated functions. Intriguingly, many of these functions ultimately impinge on cell fate decisions via apoptosis-dependent or -independent mechanisms, delineating a complex network through which Bcl-2 family members regulate cell survival and death. Here, we critically discuss the mechanisms through which Bcl-2 proteins influence cell fate as they regulate autophagy, cellular senescence, inflammation, bioenergetic metabolism, Ca fluxes, and redox homeostasis.

摘要

Bcl-2 蛋白被广泛认为是线粒体外膜通透性的关键控制器,这可以说是细胞凋亡的最重要步骤。越来越多的证据表明,Bcl-2 蛋白家族的大多数(如果不是全部)成员还介导了许多与细胞凋亡无关的功能。有趣的是,这些功能中的许多最终通过细胞凋亡依赖或非依赖机制影响细胞命运决定,描绘了一个复杂的网络,通过该网络,Bcl-2 家族成员调节细胞存活和死亡。在这里,我们批判性地讨论了 Bcl-2 蛋白通过调节自噬、细胞衰老、炎症、生物能代谢、Ca 流和氧化还原平衡来影响细胞命运的机制。

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