The mitochondrial unfolded protein response and increased longevity: Cause, consequence, or correlation?

被引:45
作者
Bennett, Christopher F. [1 ,2 ]
Kaeberlein, Matt [1 ]
机构
[1] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
[2] Univ Washington, Mol & Cellular Biol Program, Seattle, WA 98195 USA
关键词
Mitochondrial unfolded protein response; C; elegans; ATFS-1; Prohibitins; HSP-6; REPLICATIVE LIFE-SPAN; CAENORHABDITIS-ELEGANS; ELECTRON-TRANSPORT; CATALASE; OVEREXPRESSION; PROHIBITINS; RESPIRATION; INHIBITION; COMPLEX; EXPRESSION;
D O I
10.1016/j.exger.2014.02.002
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The mitochondrial unfolded protein response is a conserved pathway that allows mitochondrial chaperones and other factors to be induced in response to mitochondrial dysfunction. Activation of this pathway has been proposed to underlie lifespan extension from knockdown or mutation of several nuclear encoded mitochondrial genes in Caenorhabditis elegans. In some cases, however, induction of the mitochondrial unfolded protein response is associated with a reduction of lifespan in both yeast and C elegans. It also has yet to be demonstrated that induction of the mitochondrial unfolded protein response is sufficient to increase lifespan in the absence of overt mitochondrial dysfunction. In this perspective, we briefly review the evidence for and against a direct pro-longevity role of the mitochondrial unfolded protein response and suggest important areas of investigation for experimentally addressing this question. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:142 / 146
页数:5
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