Heat shock protein 70 inhibits cardiomyocyte necroptosis through repressing autophagy in myocardial ischemia/reperfusion injury

Irreversible damage of cardiac function arisen from myocardial ischemia/reperfusion injury (MIRI) leads to an emerging challenge in the treatments of cardiac ischemic diseases. Molecular chaperone heat shock protein 70 (HSP70) attenuates heat-stimulated cell autophagy, apoptosis, and damage in the h...

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Veröffentlicht in:	In vitro cellular & developmental biology. Animal 2016-06, Vol.52 (6), p.690-698
Hauptverfasser:	Liu, Xiaojuan, Zhang, Chao, Zhang, Chi, Li, Jingjing, Guo, Wanwan, Yan, Daliang, Yang, Chen, Zhao, Jianhua, Xia, Tian, Wang, Yuqing, Xu, Rong, Wu, Xiang, Shi, Jiahai
Format:	Artikel
Sprache:	eng
Schlagworte:	Animal Genetics and Genomics Animals Autophagy - physiology Biomedical and Life Sciences CELL AND TISSUE MODELS Cell Biology Cell Culture Cell Hypoxia Developmental Biology Down-Regulation Gene Knockdown Techniques HSP70 Heat-Shock Proteins - antagonists & inhibitors HSP70 Heat-Shock Proteins - genetics HSP70 Heat-Shock Proteins - physiology Immunohistochemistry Life Sciences Microtubule-Associated Proteins - genetics Microtubule-Associated Proteins - metabolism Myocardial Reperfusion Injury - pathology Myocytes, Cardiac - metabolism Myocytes, Cardiac - pathology Necrosis - physiopathology Protein-Serine-Threonine Kinases Rats Rats, Sprague-Dawley Stem Cells
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