A-769662 protects osteoblasts from hydrogen dioxide-induced apoptosis through activating of AMP-activated protein kinase (AMPK)

A-769662 通过激活 AMP 活化蛋白激酶 (AMPK) 保护成骨细胞免受过氧化氢诱导的细胞凋亡

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作者:Yalong Zhu, Jianhua Zhou, Rongguang Ao, Baoqing Yu

Abstract

Here we report that 5'-monophosphate (AMP)-activated protein kinase (AMPK) agonist A-769662 inhibited hydrogen peroxide (H&sub2;O&sub2;)-induced viability loss and apoptosis of human and mouse osteoblast cells. H&sub2;O&sub2;-induced moderate AMPK activation in osteoblast cells, which was enhanced by A-769662. Inactivation of AMPK by its inhibitor compound C, or by target shRNA-mediated silencing and kinase dead (KD) mutation exacerbated H&sub2;O&sub2;-induced cytotoxicity in osteoblast cells. A-769662-mediated protective effect against H&sub2;O&sub2; was also blocked by AMPK inhibition or depletion. A-769662 inhibited reactive oxygen species (ROS) accumulation by H&sub2;O&sub2; in osteoblast cells. Meanwhile, H&sub2;O&sub2;-induced ATP depletion was inhibited by A-769662, but was aggravated by compound C. Further, H&sub2;O&sub2; induced AMPK-dependent and pro-survival autophagy in cultured osteoblast cells, which was enhanced by A-769662. Our results suggested that activation of AMPK by H&sub2;O&sub2; is anti-apoptosis and pro-survival in osteoblast cells, probably due to its anti-oxidant, pro-autophagy and ATP preservation abilities, and A-769662-mediated cell-protective effect in osteoblast cells requires AMPK activation. Our study suggests that A-769662 might be further investigated as a novel anti-osteonecrosis agent.

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