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

机译:六价铬(VI)诱导的自噬通过ROS-AKT-mTOR途径保护L-02肝细胞免于凋亡。

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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 dichloro-dihydrofluorescein 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.
机译:背景/目的六价铬[Cr(VI)]污染已成为全球生态系统和人类健康关注的问题。我们先前的研究表明Cr(VI)可以诱导L-02肝细胞凋亡和自噬。在这里,我们试图探索Cr(VI)诱导自噬的潜在机制及其在细胞死亡中的确切作用。方法在透射电镜(TEM)下观察自噬的超微结构,用双标签的mCherry绿色荧光蛋白(GFP)-微管相关蛋白1轻链3(LC3),长寿蛋白降解法测定自噬通量,溶酶体抑制剂bafilomycin A1(BafA1)存在下进行LC3II表达测定。使用荧光探针二氯二氢荧光素二乙酸酯(DCFH-DA)测定活性氧(ROS)的水平。使用实时检测Beclin-1,LC3,p62 / SQSTM1和雷帕霉素(mTOR)途径相关分子的AKT哺乳动物靶标的表达水平,包括磷酸化(p)-AKT,AKT,p-mTOR和mTOR聚合酶链反应(RT-PCR)和蛋白质印迹。使用膜联蛋白V-异硫氰酸荧光素(FITC)/碘化丙啶(PI)染色确定细胞凋亡。结果我们的结果表明,L-02肝细胞中的Cr(VI)暴露激活了自噬,这由自噬体的积累,LC3-II的增加和p62 / SQSTM1的降解以及蛋白质总体降解的增强所证明。我们还证实了Cr(VI)诱导的LC3-II升高主要来自自噬诱导而不是溶酶体降解损伤。 ROS-AKT-mTOR途径与Cr(VI)诱导的自噬相关,ROS清除剂N-乙酰半胱氨酸(NAC)预处理通过减轻AKT-mTOR途径的抑制作用来抑制Cr(VI)诱导的自噬。自噬抑制剂3-甲基腺嘌呤(3-MA)和氯喹二磷酸(CDP)促进Cr(VI)诱导的细胞凋亡死亡。结论这些发现表明Cr(VI)诱导的自噬可通过ROS-AKT-mTOR通路保护L-02肝细胞免于凋亡。

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