Role of BNIP3 and NIX in cell death, autophagy, and mitophagy

被引:771
作者
Zhang, J. [1 ,2 ]
Ney, P. A. [1 ]
机构
[1] St Jude Childrens Hosp, Dept Biochem, Memphis, TN 38117 USA
[2] Univ Tennessee, Hlth Sci Ctr, Integrated Program Biomed Sci, Memphis, TN 38126 USA
基金
美国国家卫生研究院;
关键词
BNIP3; NIX; autophagy; mitophagy; MITOCHONDRIAL PERMEABILITY TRANSITION; BH3-ONLY PROTEIN BNIP3; MALIGNANT GLIOMA-CELLS; BCL-2; PROTEINS; BH3; DOMAIN; RETICULOCYTE MATURATION; TRANSMEMBRANE DOMAIN; TUMOR-SUPPRESSOR; ERYTHROID-DIFFERENTIATION; ENDOPLASMIC-RETICULUM;
D O I
10.1038/cdd.2009.16
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
BNIP3 and NIX are proteins related to the BH3-only family, which induce both cell death and autophagy. Consistent with their ability to induce cell death, BNIP3 and NIX are implicated in the pathogenesis of cancer and heart disease. In tumor cells, BNIP3 and NIX are regulated by hypoxia, and the deregulation of BNIP3 or NIX expression is associated with tumor growth. In heart muscle, BNIP3 and NIX are regulated by hypoxia and G alpha q-dependent signaling, respectively, and their expression is associated with decreased myocardial function. Apart from their role in cell death, BNIP3 and NIX are also implicated in the induction of autophagy. In erythroid cells, NIX is required for a specialized type of autophagy that targets mitochondria for elimination (mitophagy). Similarly, BNIP3 regulates mitophagy in response to hypoxia. In this review, we will discuss possible mechanisms by which BNIP3 and NIX induce cell death and mitophagy. We will also consider the potential relationship between cell death pathways and autophagy in development and homeostasis. Cell Death and Differentiation (2009) 16, 939-946; doi: 10.1038/cdd.2009.16; published online 20 February 2009
引用
收藏
页码:939 / 946
页数:8
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