自噬
基因敲除
肌肉肥大
细胞生物学
细胞凋亡
苯肾上腺素
PI3K/AKT/mTOR通路
内科学
化学
医学
内分泌学
心肌肥大
生物
信号转导
生物化学
血压
作者
Chen Liu,Ruicong Xue,Dexi Wu,Lingling Wu,Cong Chen,Weiping Tan,Yili Chen,Yugang Dong
标识
DOI:10.1016/j.bbrc.2014.10.079
摘要
Cardiac hypertrophy is a major risk factor of cardiovascular morbidity and mortality. Autophagy is established to be involved in regulating cardiac hypertrophy. REDD1, a stress-responsive protein, is proved to contribute in autophagy induction. However, the role of REDD1 in cardiac hypertrophy remains unknown. Our study demonstrated that REDD1 knockdown by RNAi exacerbated phenylephrine (PE)-induced cardiac hypertrophy, manifested by increased hypertrophic markers such as ANP and cell surface area. In addition, we discovered that ERK1/2 signaling pathway was involved in the effect of REDD1 on hypertrophy. Moreover, our study showed that REDD1 knockdown impaired autophagy in hypertrophied cardiomyocytes. mTOR, a signaling molecule governing autophagy induction, was activated by the knockdown of REDD1 under PE stress. Importantly, the pro-hypertrophic effect of REDD1 knockdown was significantly reversed by the autophagy enhancer rapamycin. Taken together, we firstly prove that REDD1 is essential for inhibiting cardiac hypertrophy by enhancing autophagy.
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