Hypoxia Induces Autophagic Cell Death through Hypoxia-Inducible Factor 1α in Microglia

被引:73
|
作者
Yang, Zhao [1 ]
Zhao, Tian-zhi [2 ]
Zou, Yong-jie [1 ]
Zhang, John H. [1 ]
Feng, Hua [1 ]
机构
[1] Third Mil Med Univ, Southwest Hosp, Dept Neurosurg, Chongqing, Peoples R China
[2] Fourth Mil Med Univ, Tangdu Hosp, Dept Neurosurg, Xian, Shaanxi Provinc, Peoples R China
来源
PLOS ONE | 2014年 / 9卷 / 05期
基金
中国国家自然科学基金;
关键词
IN-VIVO; CEREBRAL-ISCHEMIA; STROKE; ACTIVATION; INJURY; BRAIN; METABOLISM; EXPRESSION; TARGET; GROWTH;
D O I
10.1371/journal.pone.0096509
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
As phagocytic cells of central nervous system, excessive activation or cell death of microglia is involved in a lot of nervous system injury and degenerative disease, such as stroke, epilepsy, Parkinson's disease, Alzheimer's disease. Accumulating evidence indicates that hypoxia upregulates HIF-1 alpha expression leading to cell death of microglia. However, the exact mechanism of cell death induced by hypoxia in microglia is not clear. In the current study, we showed that hypoxia induced cell death and autophagy in microglia. The suppression of autophagy using either pharmacologic inhibitors (3-methyladenine, bafilomycin A1) or RNA interference in essential autophagy genes (BECN1 and ATG5) decreased the cell death induced by hypoxia in microglia cells. Moreover, the suppression of HIF-1 alpha using either pharmacologic inhibitors 3-MA, Baf A1) or RNA interference decreased the microglia death and autophagy in vitro. Taken together, these data indicate that hypoxia contributes to autophagic cell death of microglia through HIF-1 alpha, and provide novel therapeutic interventions for cerebral hypoxic diseases associated with microglia activation.
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页数:9
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