自噬
ATG5型
SH-SY5Y型
吗啡
基因敲除
程序性细胞死亡
生物
细胞生物学
药理学
神经毒性
神经母细胞瘤
海马体
细胞凋亡
细胞培养
内分泌学
内科学
医学
生物化学
毒性
遗传学
作者
Lixia Zhao,Yushan Zhu,Dongmei Wang,Ming Chen,Ping Gao,Weiming Xiao,Guanhua Rao,Xiaohui Wang,Haijing Jin,Lin Xu,Nan Sui,Quan Chen
出处
期刊:Autophagy
[Taylor & Francis]
日期:2010-04-01
卷期号:6 (3): 386-394
被引量:76
标识
DOI:10.4161/auto.6.3.11289
摘要
Chronic exposure to morphine can induce drug addiction and neural injury, but the exact mechanism is not fully understood. Here we show that morphine induces autophagy in neuroblastoma SH-SY5Y cells and in the rat hippocampus. Pharmacological approach shows that this effect appears to be mediated by PTX-sensitive G protein-coupled receptors signaling cascade. Morphine increases Beclin 1 expression and reduces the interaction between Beclin 1 and Bcl-2, thus releasing Beclin 1 for its pro-autophagic activity. Bcl-2 overexpression inhibits morphine-induced autophagy, whereas knockdown of Beclin 1 or knockout of ATG5 prevents morphine-induced autophagy. In addition, chronic treatment with morphine induces cell death, which is increased by autophagy inhibition through Beclin 1 RNAi. Our data are the first to reveal that Beclin 1 and ATG5 play key roles in morphine-induced autophagy, which may contribute to morphine-induced neuronal injury.
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