Mechanisms, pathophysiological roles and methods for analyzing mitophagy - recent insights

被引:77
|
作者
Williams, Jessica A. [1 ]
Ding, Wen-Xing [1 ]
机构
[1] Univ Kansas, Med Ctr, Dept Pharmacol Toxicol & Therapeut, 3901 Rainbow Blvd, Kansas City, KS 66160 USA
关键词
autophagy; mitophagy; Mito-QC; mitoTimer; mt-Keima; Parkin; MITOCHONDRIAL QUALITY-CONTROL; ETHANOL-INDUCED AUTOPHAGY; TUMOR-SUPPRESSOR GENE; INDUCED LIVER-INJURY; REGULATES MITOPHAGY; ENDOPLASMIC-RETICULUM; SELECTIVE AUTOPHAGY; PINK1/PARKIN-MEDIATED MITOPHAGY; JUVENILE PARKINSONISM; MEDIATES MITOPHAGY;
D O I
10.1515/hsz-2017-0228
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In 2012, we briefly summarized the mechanisms, pathophysiological roles and methods for analyzing mitophagy. As then, the mitophagy field has continued to grow rapidly, and many new molecular mechanisms regulating mitophagy and molecular tools for monitoring mitophagy have been discovered and developed. Therefore, the purpose of this review is to update information regarding these advances in mitophagy while focusing on basic molecular mechanisms of mitophagy in different organisms and its pathophysiological roles. We also discuss the advantage and limitations of current methods to monitor and quantify mitophagy in cultured cells and in vivo mouse tissues.
引用
收藏
页码:147 / 178
页数:32
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