1. Academic Validation
  2. Regulation of autophagy by Beclin 1 in the heart

Regulation of autophagy by Beclin 1 in the heart

  • J Mol Cell Cardiol. 2016 Jun:95:19-25. doi: 10.1016/j.yjmcc.2015.10.032.
Yasuhiro Maejima 1 Mitsuaki Isobe 2 Junichi Sadoshima 3
Affiliations

Affiliations

  • 1 Department of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers-New Jersey Medical School, Newark, NJ, USA; Department of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.
  • 2 Department of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.
  • 3 Department of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers-New Jersey Medical School, Newark, NJ, USA. Electronic address: [email protected].
Abstract

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 1'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/XL) 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 1's interaction with Bcl-2/XL 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.

Keywords

Apoptosis; Autophagy; Bcl-2 family proteins; Beclin 1; Phosphorylation.

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