| Literature DB >> 25086229 |
Cheng Shen1, Cong Wang1, Fan Fan1, Zhiyin Yang2, Quan Cao1, Xiangwei Liu1, Xiaolei Sun1, Xiaona Zhao1, Peng Wang1, Xin Ma1, Hong Zhu1, Zhen Dong1, Yunzeng Zou3, Kai Hu1, Aijun Sun4, Junbo Ge3.
Abstract
Mitochondrial aldehyde dehydrogenase 2 (ALDH2) was demonstrated to play cardioprotective roles in cardiovascular diseases. Nonetheless, little is known about the roles and mechanisms of ALDH2 in pressure overload-induced cardiac damages. In this study, we revealed that ALDH2 deficiency overtly exacerbated transverse aortic constriction (TAC)-induced cardiac dysfunction. Cardiomyocyte enlargement was observed in both WT and ALDH2-/- mice in HE-stained myocardial tissue samples at 8 weeks post TAC surgery. Mitochondrial morphology and structure were also significantly damaged post TAC surgery and the changes were aggravated in ALDH2-/- TAC hearts. ALDH2 deficiency also depressed myocardial autophagy in hearts at 8 weeks post TAC surgery with a potential mechanism of repressing the expression of Beclin-1 and promoting the interaction between Bcl-2 and Beclin-1. These data indicate that ALDH2 deficiency exacerbates the pressure overload induced cardiac dysfunction partly by inhibiting Beclin-1 dependent autophagy pathway. This article is part of a Special Issue entitled: Autophagy and protein quality control in cardiometabolic diseases.Entities:
Keywords: ALDH2; Autophagy; Beclin-1; Heart failure; Pressure overload
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Year: 2014 PMID: 25086229 DOI: 10.1016/j.bbadis.2014.07.014
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002