自噬
氧化应激
缺氧(环境)
细胞凋亡
细胞生物学
活性氧
化学
生物
生物化学
氧气
有机化学
作者
Qing-Min Feng,Yang Shao,Rong Jiao,Hongwei Wei,Dai Ming-qiang,Huixing Xie,Caixia Xu,Ji-Ke Li
出处
期刊:Advances in Biological Chemistry
[Scientific Research Publishing, Inc.]
日期:2019-01-01
卷期号:09 (02): 54-67
被引量:3
标识
DOI:10.4236/abc.2019.92005
摘要
Coronary heart disease (CHD) is a hypoxia related disease. However, the relationship of the hypoxia-induced oxidative stress, autophagy and apoptosis in cardiomyocyte remains unclear. In this study, we used CoCl2 to mimic hypoxic conditions in H9c2 cardiomyocytes and study the effects of CoCl2-induced hypoxia on oxidative stress, apoptosis and autophagy, as well as the relationships among these processes. Cell viability and levels of ROS, LC3-II, p62, caspase-3 and PARP were assessed. The viability and morphology of cardiomyocytes were affected by hypoxia, and hypoxia enhanced levels of ROS and the levels of the LC3-II, p62, caspase-3 and PARP proteins in H9c2 cells in a dose-dependent manner. ROS levels rise gradually in the presence of hypoxia; however, it shrinks when hypoxia reaches a certain level. Caspase-3 and PARP levels were raised with the increasing of hypoxia level. Enhanced level of LC3 and decreased levels of p62 in hypoxic cells indicate that autophagy levels are in accord with hypoxia. Based on these results, hypoxia induces oxidative stress, apoptosis and autophagy in cardiomyocytes. Autophagy is a double-edged sword. At a low level, autophagy can resist oxidative stress and protect cardiomyocytes from oxidative stress, while high level autophagy can promote apoptosis of cardiomyocytes.
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