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AMP-activated protein kinase-dependent autophagy mediated the protective effect of sonic hedgehog pathway on oxygen glucose deprivation-induced injury of cardiomyocytes

机译:AMP激活的蛋白激酶依赖性自噬介导声波刺猬通路对氧葡萄糖剥夺所致心肌细胞损伤的保护作用

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摘要

Sonic hedgehog (Shh) pathway has been reported to protect cardiomyocytes in myocardial infarction (MI), but the underlying mechanism is not clear. Here, we provide evidence that Shh pathway induces cardiomyocytes survival through AMP-activated protein kinase-dependent autophagy. Shh pathway agonist SAG increased the expression of LC3-II, and induced the formation of autophagosomes in cultured H9c2 cardiomyocytes under oxygen glucose deprivation (OGD) 1 h and 4 h. Moreover, SAG induced a profound AMP-activated protein kinase (AMPK) activation, and then directly phosphorylated and activated the downstream autophagy initiator Ulk1, independent of the autophagy suppressor mammalian target of rapamycin (mTOR) complex 1. Taken together, our results have shown that Shh activates AMPK-dependent autophagy in cardiomyocytes under OGD, suggesting a role of autophagy in Shh-induced cellular protection. (C) 2015 Elsevier Inc. All rights reserved.
机译:据报道,声波刺猬(Shh)途径可保护心肌梗死(MI)中的心肌细胞,但其潜在机制尚不清楚。在这里,我们提供证据表明Shh途径通过AMP激活的蛋白激酶依赖性自噬诱导心肌细胞存活。 Shh通路激动剂SAG在氧葡萄糖剥夺(OGD)1 h和4 h下增加了培养的H9c2心肌细胞中LC3-II的表达,并诱导了自噬体的形成。此外,SAG诱导了深刻的AMP激活的蛋白激酶(AMPK)激活,然后直接磷酸化并激活了下游自噬引发剂Ulk1,而与雷帕霉素(mTOR)复合物1的自噬抑制剂哺乳动物靶标无关。综上所述,我们的结果表明Shh在OGD下激活心肌细胞中AMPK依赖性自噬,提示自噬在Shh诱导的细胞保护中的作用。 (C)2015 Elsevier Inc.保留所有权利。

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