Mitochondrial Proteolysis and Metabolic Control

被引:23
作者
Ahola, Sofia [1 ]
Langer, Thomas [1 ]
MacVicar, Thomas [1 ]
机构
[1] Max Planck Inst Biol Ageing, Dept Mitochondria Proteostasis, D-50931 Cologne, Germany
关键词
RESPIRATORY-CHAIN COMPLEXES; UNFOLDED PROTEIN RESPONSE; TRANSFER-RNA SYNTHETASE; LON PROTEASE; TRANSCRIPTION FACTOR; HEARING-LOSS; PHOSPHATIDYLSERINE DECARBOXYLASE; DEPENDENT DEGRADATION; PROCESSING PEPTIDASE; SPASTIC PARAPLEGIA;
D O I
10.1101/cshperspect.a033936
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondria are metabolic hubs that use multiple proteases to maintain proteostasis and to preserve their overall quality. A decline of mitochondrial proteolysis promotes cellular stress and may contribute to the aging process. Mitochondrial proteases have also emerged as tightly regulated enzymes required to support the remarkable mitochondrial plasticity necessary for metabolic adaptation in a number of physiological scenarios. Indeed, the mutation and dysfunction of several mitochondrial proteases can cause specific human diseases with severe metabolic phenotypes. Here, we present an overview of the proteolytic regulation of key mitochondrial functions such as respiration, lipid biosynthesis, and mitochondrial dynamics, all of which are required for metabolic control. We also pay attention to how mitochondrial proteases are acutely regulated in response to cellular stressors or changes in growth conditions, a greater understanding of which may one day uncover their therapeutic potential.
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页数:19
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