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The role of autophagic and lysosomal pathways in ischemic brain injury
by
Zhaohua Gu Yinyi Sun Kangyong Liu Fen Wang Ting Zhang Qiang Li Liwei Shen Ling Zhou Liang Dong Nan Shi Qian zhang Wei Zhang Meizhen Zhao Xiaojiang Sun
in
Apoptosis
/ Autophagy
/ Autophagy (Cytology)
/ Brain
/ Cellular signal transduction
/ Cytoplasm
/ Hypoxia
/ Injuries
/ Ischemia
/ Light
/ Lysosomes
/ Mammals
/ Microscopy
/ Physiological aspects
/ Proteins
/ Research and Report : Ischemic Brain Injury and Neural Regeneration
/ Surgery
/ Traumatic brain injury
/ Western印迹
/ 共聚焦显微镜
/ 溶酶体
/ 神经细胞死亡
/ 组织蛋白酶B
/ 缺血性脑损伤
/ 自噬
/ 透射电子显微镜
2013
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The role of autophagic and lysosomal pathways in ischemic brain injury
by
Zhaohua Gu Yinyi Sun Kangyong Liu Fen Wang Ting Zhang Qiang Li Liwei Shen Ling Zhou Liang Dong Nan Shi Qian zhang Wei Zhang Meizhen Zhao Xiaojiang Sun
in
Apoptosis
/ Autophagy
/ Autophagy (Cytology)
/ Brain
/ Cellular signal transduction
/ Cytoplasm
/ Hypoxia
/ Injuries
/ Ischemia
/ Light
/ Lysosomes
/ Mammals
/ Microscopy
/ Physiological aspects
/ Proteins
/ Research and Report : Ischemic Brain Injury and Neural Regeneration
/ Surgery
/ Traumatic brain injury
/ Western印迹
/ 共聚焦显微镜
/ 溶酶体
/ 神经细胞死亡
/ 组织蛋白酶B
/ 缺血性脑损伤
/ 自噬
/ 透射电子显微镜
2013
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The role of autophagic and lysosomal pathways in ischemic brain injury
by
Zhaohua Gu Yinyi Sun Kangyong Liu Fen Wang Ting Zhang Qiang Li Liwei Shen Ling Zhou Liang Dong Nan Shi Qian zhang Wei Zhang Meizhen Zhao Xiaojiang Sun
in
Apoptosis
/ Autophagy
/ Autophagy (Cytology)
/ Brain
/ Cellular signal transduction
/ Cytoplasm
/ Hypoxia
/ Injuries
/ Ischemia
/ Light
/ Lysosomes
/ Mammals
/ Microscopy
/ Physiological aspects
/ Proteins
/ Research and Report : Ischemic Brain Injury and Neural Regeneration
/ Surgery
/ Traumatic brain injury
/ Western印迹
/ 共聚焦显微镜
/ 溶酶体
/ 神经细胞死亡
/ 组织蛋白酶B
/ 缺血性脑损伤
/ 自噬
/ 透射电子显微镜
2013
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The role of autophagic and lysosomal pathways in ischemic brain injury
Journal Article
The role of autophagic and lysosomal pathways in ischemic brain injury
2013
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Overview
Autophagy is involved in neural cell death after cerebral ischemia. Our previous studies showed that rapamycin-induced autophagy decreased the rate of apoptosis, but the rate of apoptosis was in- creased after the autophagy inhibitor, 3-methyladenine, was used. In this study, a suture-occluded method was performed to generate a rat model of brain ischemia. Under a transmission electron microscope, autophagic bodies and autophagy lysosomes were markedly accumulated in neurons at 4 hours post brain ischemic injury, with their numbers gradually reducing over time. Western blotting demonstrated that protein levels of light chain 3-11 and cathepsin B were significantly in- creased within 4 hours of ischemic injury, but these levels were not persistently upregulated over time. Confocal microscopy showed that autophagy was mainly found in neurons with positive light chain 3 signal. Injection of rapamycin via tail vein promoted the occurrence of autophagy in rat brain tissue after cerebral ischemia and elevated light chain 3 and cathepsin B expression. However, in- jection of 3-methyladenine significantly diminished light chain 3-11 and cathepsin B expression. Results verified that autophagic and lysosomal activity is increased in ischemic neurons. Abnormal components in cells can be eliminated through upregulating cell autophagy or inhibiting autophagy after ischemic brain injury, resulting in a dynamic balance of substances in cells. Moreover, drugs that interfere with autophagy may be potential therapies for the treatment of brain injury.
Publisher
Medknow Publications and Media Pvt. Ltd,Medknow Publications & Media Pvt. Ltd,Department of Neurology, Shanghai Pudong New Area Zhoupu Hospital, Shanghai 234318, China%Department of Neurology, the Sixth People’s Hospital of Shanghai, Shanghai Jiao Tong University, Shanghai 200233, China%Department of Neurobiology, Suzhou University School of Medicine, Suzhou 215123, Jiangsu Province, China%Department of Neurology, the Fifth People’s Hospital of Shanghai, Fudan University, Shanghai 200240, China,Medknow Publications & Media Pvt Ltd
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