TY - JOUR
T1 - Hypoxia induces autophagic cell death through hypoxia-inducible factor 1α in microglia
AU - Yang, Zhao
AU - Zhao, Tian Zhi
AU - Zou, Yong Jie
AU - Zhang, John H.
AU - Feng, Hua
N1 - Ischemic stroke, the most common acute cerebrovascular disease with high morbidity and mortality, is one of the leading causes of human deaths[1], [2], [3]. The pathogenesis of this disease has not been elucidated yet. Ischemic/hypoxic injury of brain tissues and subsequent necrosis and inflammation of nerve cells had long been considered the principal pathophysiological mechanism of cerebral infarction[4].
PY - 2014/5/12
Y1 - 2014/5/12
N2 - 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-1α 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-1α 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-1α, and provide novel therapeutic interventions for cerebral hypoxic diseases associated with microglia activation.
AB - 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-1α 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-1α 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-1α, and provide novel therapeutic interventions for cerebral hypoxic diseases associated with microglia activation.
KW - Cell Line
KW - Microscopy, Electron, Transmission
KW - Enzyme-Linked Immunosorbent Assay
KW - Humans
KW - Autophagy/drug effects
KW - Cell Hypoxia/physiology
KW - Hypoxia-Inducible Factor 1, alpha Subunit/metabolism
KW - Microglia/cytology
KW - Adenine/analogs & derivatives
UR - http://www.scopus.com/inward/record.url?scp=84901250589&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84901250589&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/cc0e5ec7-63b9-36f9-97e6-2dd15c966d2e/
U2 - 10.1371/journal.pone.0096509
DO - 10.1371/journal.pone.0096509
M3 - Article
C2 - 24818601
SN - 1932-6203
VL - 9
JO - PLoS ONE
JF - PLoS ONE
IS - 5
M1 - e96509
ER -