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Mitochondrial turnover in the heart

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出版社

ELSEVIER
DOI: 10.1016/j.bbamcr.2010.11.017

关键词

Mitochondria; Mitophagy; Autophagy; Mitochondrial turnover; Cardioprotection

资金

  1. NIH [R01 HL060590, R01 AG033283, R01 HL092136, R01 HL034579, P01 HL085577, R01 HL087023, R01 HL101217]

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Mitochondrial quality control is increasingly recognized as an essential element in maintaining optimally functioning tissues. Mitochondrial quality control depends upon a balance between biogenesis and autophagic destruction. Mitochondrial dynamics (fusion and fission) allows for the redistribution of mitochondrial components. We speculate that this permits sorting of highly functional components into one end of a mitochondrion, while damaged components are segregated at the other end, to be jettisoned by asymmetric fission followed by selective mitophagy. Ischemic preconditioning requires autophagy/mitophagy, resulting in selective elimination of damaged mitochondria, leaving behind a population of robust mitochondria with a higher threshold for opening of the mitochondrial permeability transition pore. In this review we will consider the factors that regulate mitochondrial biogenesis and destruction, the machinery involved in both processes, and the biomedical consequences associated with altered mitochondrial turnover. This article is part of a Special Issue entitled: Mitochondria and Cardioprotection. (C) 2010 Elsevier B.V. All rights reserved.

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