Cr(VI)-Induced Autophagy Protects L-02 Hepatocytes from Apoptosis Through the ROS-AKT-mTOR Pathway

被引:34
|
作者
Liang, Qi [1 ]
Xiao, Yuanyuan [2 ]
Liu, Kaihua [2 ]
Zhong, Caigao [2 ]
Zeng, Ming [2 ]
Xiao, Fang [2 ]
机构
[1] Cent South Univ, Xiangya Hosp 3, Dept Radiol, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Sch Publ Hlth, Dept Hlth Toxicol, 238 Shangmayuanling Rd, Changsha 410078, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Cr(VI); Autophagy; L-02; hepatocytes; Apoptosis; ROS; AKT-mTOR; CELL-DEATH; HEXAVALENT CHROMIUM; INHIBITION; DEGRADATION; DYSFUNCTION; ACTIVATION;
D O I
10.1159/000495713
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background/Aims: Hexavalent chromium [Cr(VI)] pollution has become a global concern for both ecosystems and human health. Our previous study revealed Cr(VI) could induce both apoptosis and autophagy in L-02 hepatocytes. Here, we sought to explore the underlying mechanism of Cr(VI)-induced autophagy and its exact role in cell death. Methods: Autophagy ultrastructure was observed under transmission electron microscope (TEM), autophagy flux was measured with double-tagged mCherry-green fluorescent protein (GFP)-microtubule-associated protein 1 light chain 3 (LC3) assay, long-lived protein degradation assay, and LC3II expression assay in the presence of lysosomal inhibitor, bafilomycin A1 (BafA1). Reactive oxygen species (ROS) level was determined using fluorescent probe dichlorodihydrofluorescein diacetate (DCFH-DA). The expression levels of Beclin-1, LC3, p62/SQSTM1, and AKT-mammalian target of rapamycin (mTOR) pathway-related molecules including phosphorylation (p)-AKT, AKT, p-mTOR, and mTOR were examined using real-time polymerase chain reaction (RT-PCR) and western blotting. Apoptosis was determined using Annexin V-fluorescein isothiocyanate (FITC)/propidium iodide (PI) staining. Results: Our results demonstrated Cr(VI) exposure activated autophagy in L-02 hepatocytes, as evidenced by the accumulation of autophagosomes, the increase of LC3-II and degradation of p62/ SQSTM1, and the enhanced overall degradation of proteins. We also confirmed Cr(VI)-induced LC3-II elevation mainly came from autophagy induction rather than lysosomal degradation impairment. ROS-AKT-mTOR pathway was associated with Cr(VI)-induced autophagy, and ROS scavenger N-acetylcysteine (NAC) pretreatment inhibited Cr(VI)-induced autophagy by alleviating the inhibition of the AKT-mTOR pathway. Autophagy inhibitors 3-methyladenine (3-MA) and chloroquine diphosphate (CDP) promoted Cr(VI)-induced apoptotic death. Conclusion: These findings indicated Cr(VI)-induced autophagy protected L-02 hepatocytes from apoptosis through the ROS-AKT-mTOR pathway. (C) 2018 The Author(s) Published by S. Karger AG, Basel.
引用
收藏
页码:1863 / 1878
页数:16
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