BH3-only proteins: Orchestrators of apoptosis

被引:266
作者
Shamas-Din, Aisha [1 ]
Brahmbhatt, Hetal [1 ]
Leber, Brian [1 ,2 ]
Andrews, David W. [1 ]
机构
[1] Dept Biochem & Biomed Sci, Hamilton, ON, Canada
[2] McMaster Univ, Dept Med, Hamilton, ON, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2011年 / 1813卷 / 04期
关键词
Apoptosis; Bcl-2 family protein; BH3-only protein; Conformational change; Autophagy; BH3; mimetic; CYTOCHROME-C RELEASE; MITOCHONDRIAL-MEMBRANE PERMEABILIZATION; BCL-2; FAMILY-MEMBERS; ENDOPLASMIC-RETICULUM; BH3; DOMAIN; BAX ACTIVATION; CELL-SURVIVAL; CONFORMATIONAL-CHANGES; ANTAGONIZES MCL-1; CRYSTAL-STRUCTURE;
D O I
10.1016/j.bbamcr.2010.11.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The BH3-only proteins of Bcl-2 family are essential initiators of apoptosis that propagate extrinsic and intrinsic cell death signals. The interaction of BH3-only proteins with other Bcl-2 family members is critical for understanding the core machinery that controls commitment to apoptosis by permeabilizing the mitochondrial outer membrane. BH3-only proteins promote apoptosis by both directly activating Bax and Bak and by suppressing the anti-apoptotic proteins at the mitochondria and the endoplasmic reticulum. To prevent constitutive cell death, BH3-only proteins are regulated by a variety of mechanisms including transcription and post-translational modifications that govern specific protein-protein interactions. Furthermore, BH3-only proteins also control the initiation of autophagy, another important pathway regulating cell survival and death. Emerging evidence indicates that the interaction of BH3-only proteins with membranes regulates binding to other Bcl-2 family members, thereby specifying function. Due to the important role of BH3-only proteins in the regulation of cell death, several promising BH3-mimetic drugs that are active in pre-clinical models are currently being tested as anti-cancer agents. This article is part of a Special Issue entitled Mitochondria: the deadly organelle. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:508 / 520
页数:13
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