Zhu Han-Hua, Wang Xian-Tao, Sun Yu-Han, He Wen-Kai, Liang Jia-Bao, Mo Bing-Hai, Li Lang
Cell Physiol Biochem. 2018;49(6):2138-2150. doi: 10.1159/000493817. Epub 2018 Sep 26.
BACKGROUND/AIMS: Microvascular obstruction (MVO), an undesirable complication of percutaneous coronary intervention, is independently associated with adverse left ventricle remodeling and poor prognosis after acute myocardial infarction. Hypoxia and oxidative stress major roles in the pathophysiology of MVO. Pim1 serves an important protective role in the ischemic myocardium, but the underlying mechanisms remain poorly defined. Autophagy in early hypoxia or during moderate oxidative stress has been demonstrated to protect the myocardium. In this study, we investigated the association between the protective effect of Pim1 and autophagy after hypoxia and oxidative stress.
Ventricular myocytes from neonatal rat heart (NRVMs) were isolated. NRVMs were exposed to hypoxia and H2O2. Rapamycin and 3-methyladenine (3-MA) were used as an activator and inhibitor of autophagy, respectively. pHBAd-Pim1 was transfected into NRVMs. We assessed cardiomyocyte apoptosis by Annexin V-FITC/PI flow cytometry. Autophagy was evaluated by mRFP-GFP-LC3 adenovirus infection by confocal microscopy. Western blotting was used to quantify apoptosis or autophagy protein (caspase-3, LC3, P62, AMPK, mTOR, ATG5) concentrations.
Autophagy and apoptosis in NRVMs significantly increased and peaked at 3 h and 6 h, respectively, after exposure to hypoxia and H2O2. The mTOR inhibitor rapamycin induced autophagy and decreased cardiomyocyte apoptosis, but the autophagy inhibitor 3-MA decreased autophagy and increased apoptosis at 3 h after exposure to hypoxia and H2O2. Pim1 levels in NRVMs increased at 3 h and decreased gradually after exposure to hypoxia and H2O2. Pim1 overexpression enhanced autophagy and decreased apoptosis. Pim1-induced promotion of autophagy is partly the result of activation of the AMPK/mTOR/ATG5 pathway after exposure to hypoxia and H2O2.
Our results revealed that Pim1 overexpression prevented NRVMs from apoptosis via upregulating autophagy after exposure to hypoxia and oxidative stress, partly through activation of the AMPK/mTOR/ATG5 autophagy pathway.
背景/目的:微血管阻塞(MVO)是经皮冠状动脉介入治疗的不良并发症,与急性心肌梗死后不良的左心室重构及预后独立相关。缺氧和氧化应激在MVO的病理生理学中起主要作用。Pim1在缺血心肌中发挥重要的保护作用,但其潜在机制仍不清楚。已证实早期缺氧或中度氧化应激期间的自噬可保护心肌。在本研究中,我们调查了缺氧和氧化应激后Pim1的保护作用与自噬之间的关联。
分离新生大鼠心脏(NRVMs)的心室肌细胞。将NRVMs暴露于缺氧和过氧化氢环境。雷帕霉素和3-甲基腺嘌呤(3-MA)分别用作自噬的激活剂和抑制剂。将pHBAd-Pim1转染到NRVMs中。通过Annexin V-FITC/PI流式细胞术评估心肌细胞凋亡。通过共聚焦显微镜用mRFP-GFP-LC3腺病毒感染评估自噬。蛋白质印迹法用于定量凋亡或自噬蛋白(半胱天冬酶-3、LC3、P62、AMPK、mTOR、ATG5)浓度。
暴露于缺氧和过氧化氢后,NRVMs中的自噬和凋亡显著增加,分别在3小时和6小时达到峰值。mTOR抑制剂雷帕霉素诱导自噬并减少心肌细胞凋亡,但自噬抑制剂3-MA在暴露于缺氧和过氧化氢3小时后减少自噬并增加凋亡。暴露于缺氧和过氧化氢后,NRVMs中的Pim1水平在3小时升高,随后逐渐下降。Pim1过表达增强自噬并减少凋亡。Pim1诱导的自噬促进部分是暴露于缺氧和过氧化氢后AMPK/mTOR/ATG5途径激活的结果。
我们的结果显示,Pim1过表达通过在暴露于缺氧和氧化应激后上调自噬来防止NRVMs凋亡,部分是通过激活AMPK/mTOR/ATG5自噬途径实现的。