Selective mitochondrial autophagy during erythroid maturation

被引:45
作者
Chen, Min [1 ]
Sandoval, Hector [1 ]
Wang, Jin [1 ]
机构
[1] Baylor Coll Med, Dept Immunol, Houston, TX 77030 USA
关键词
Nix; autophagy; erythroid maturation; Bcl-2; BH3; mitochondrial membrane potential; mitochondrial quality control;
D O I
10.4161/auto.6716
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Accumulating evidence suggests that autophagy can be selective in the clearance of organelles in yeast and in mammalian cells. We have observed that the sequestration of mitochondria by autophagosomes was defective in reticulocytes in the absence of Nix. Nix is required for the dissipation of mitochondrial membrane potential (Delta Psi m) during erythroid maturation. Moreover, pharmacological agents that induce the loss of Delta Psi m can restore the sequestration of mitochondria by autophagosomes and promote mitochondrial clearance in Nix(-/-) erythroid cells. Our data suggest that mitochondrial depolarization induces recognition and sequestration of mitochondria by autophagosomes. Elucidating the mechanisms underlying selective mitochondrial autophagy not only will help us to understand the mechanisms for erythroid maturation, but also may provide insights into mitochondrial quality control by autophagy in the protection against aging, cancer and neurodegenerative diseases.
引用
收藏
页码:926 / 928
页数:3
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