Regulation of autophagy by Beclin 1 in the heart

被引:199
作者
Maejima, Yasuhiro [1 ,2 ]
Isobe, Mitsuaki [2 ]
Sadoshima, Junichi [1 ]
机构
[1] Rutgers New Jersey Med Sch, Dept Cell Biol & Mol Med, Cardiovasc Res Inst, 185 South Orange Ave,MSB G-609, Newark, NJ 07103 USA
[2] Tokyo Med & Dent Univ, Dept Cardiovasc Med, Tokyo, Japan
关键词
Autophagy; Beclin; 1; Bcl-2 family proteins; Phosphorylation; Apoptosis; ACTIVATED PROTEIN-KINASE; PHOSPHATIDYLINOSITOL 3-KINASE COMPLEXES; BCL-X-L; CELL-DEATH; PRESSURE-OVERLOAD; CARDIAC-HYPERTROPHY; INHIBITS AUTOPHAGY; BH4; DOMAIN; APOPTOSIS; PHOSPHORYLATION;
D O I
10.1016/j.yjmcc.2015.10.032
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dysregulation of autophagy in cardiomyocytes is implicated in various heart disease conditions. Beclin 1, a mammalian ortholog of yeast Atg6 and a core component of the autophagy machinery, plays a central role in the regulation of autophagy through activation of Vps34. Beclin l's ability to activate Vps34 is tightly regulated via transcriptional regulation, miRNA, post -translational modification, and interaction with Beclin 1 binding proteins. Of these mechanisms, binding of Beclin 1 with Bcl-2 family proteins (Bcl-2/X-L) that negatively regulate autophagy activity has been shown to be both positively and negatively regulated by various kinases, including DAPK, ROCK1, Mst1 and JNK1, in response to external stimuli. Beclin l's interaction with Bcl-2/X-L also secondarily affects apoptosis through regulation of pro-apoptotic BH3 domain containing proteins. Thus, modulation of Beclin 1 significantly influences both autophagy and apoptosis, thereby deeply affecting the survival and death of cardiomyocytes in the heart. In this review, we discuss the signaling mechanism of autophagy modulation through Beclin 1 and therapeutic potential of Beclin 1 in heart diseases. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:19 / 25
页数:7
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