Inhibition of mitochondrial genome expression triggers the activation of CHOP-10 by a cell signaling dependent on the integrated stress response but not the mitochondrial unfolded protein response

被引:69
|
作者
Michel, Sebastien [1 ]
Canonne, Morgane [1 ]
Arnould, Thierry [1 ]
Renard, Patricia [1 ]
机构
[1] Univ Namur, NARILIS, Lab Biochem & Cell Biol URBC, B-5000 Namur, Belgium
关键词
Mitochondrial dysfunction; Mitochondria unfolded protein response (mtUPR); Integrated stress response (ISR); C/EBP homologous protein 10 (CHOP-10); mtDNA depletion; Doxycycline; RAT PRIMARY HEPATOCYTES; OXIDATIVE STRESS; GENE-EXPRESSION; KINASE GCN2; INDUCTION; PHOSPHORYLATION; TRANSCRIPTION; TRANSLATION; PATHWAY; MELAS;
D O I
10.1016/j.mito.2015.01.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondria-to-nucleus communication, known as retrograde signaling, is important to adjust the nuclear gene expression in response to organelle dysfunction. Among the transcription factors described to respond to mito-chondrial stress, CHOP-10 is activated by respiratory chain inhibition, mitochondrial accumulation of unfolded proteins and mtDNA mutations. In this study, we show that altered/impaired expression of mtDNA induces CHOP-10 expression in a signaling pathway that depends on the eIF2 alpha/ATF4 axis of the integrated stress response rather than on the mitochondrial unfolded protein response. (C) 2015 Elsevier B.V. and Mitochondria Research Society. All rights reserved.
引用
收藏
页码:58 / 68
页数:11
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