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Bcl-2对线粒体能量代谢的调控。

Bcl-2 regulation of mitochondrial energetics.

作者信息

Murphy Elizabeth, Imahashi Ken-ichi, Steenbergen Charles

机构信息

Laboratory of Signal Transduction, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709, USA.

出版信息

Trends Cardiovasc Med. 2005 Nov;15(8):283-90. doi: 10.1016/j.tcm.2005.09.002.

Abstract

Recent data suggest that in addition to regulating apoptosis, Bcl-2 (an anti-apoptotic protein overexpressed in B-cell lymphoma) and Bcl-2 family members also regulate mitochondrial and cell physiology. t-Bid, a Bcl-2 family member, has been shown to modulate reorganization of mitochondrial cristae. Bcl-2 appears to regulate voltage-dependent anion channel permeability, which has important consequences for mitochondrial transport of adenine nucleotides, Ca(2+), and other metabolites. BAD, a pro-apoptotic Bcl-2 family member, is required for the binding of glucokinase to a mitochondrial complex, and BAD null mice have altered glucose homeostasis. It has been suggested that Bcl-2 family members may regulate important mitochondrial/cell functions and serve as sentinels to detect abnormalities in these pathways and, when the abnormalities are severe enough, to initiate or facilitate cell death. Understanding the physiologic processes controlled by Bcl-2 will be important in understanding cell regulation, and it may also provide new insights into the regulation of apoptosis.

摘要

最近的数据表明,除了调节细胞凋亡外,Bcl-2(一种在B细胞淋巴瘤中过表达的抗凋亡蛋白)和Bcl-2家族成员还调节线粒体和细胞生理。t-Bid是一种Bcl-2家族成员,已被证明可调节线粒体嵴的重组。Bcl-2似乎调节电压依赖性阴离子通道通透性,这对腺嘌呤核苷酸、Ca(2+)和其他代谢物的线粒体转运具有重要影响。BAD是一种促凋亡的Bcl-2家族成员,是葡萄糖激酶与线粒体复合物结合所必需的,BAD基因敲除小鼠的葡萄糖稳态发生了改变。有人提出,Bcl-2家族成员可能调节重要的线粒体/细胞功能,并作为哨兵来检测这些途径中的异常情况,当异常情况严重到一定程度时,启动或促进细胞死亡。了解Bcl-2所控制的生理过程对于理解细胞调节很重要,它也可能为细胞凋亡的调节提供新的见解。

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