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ATF6 在 Cr(VI)诱导的 DF-1 细胞凋亡中的作用。

The role of ATF6 in Cr(VI)-induced apoptosis in DF-1 cells.

机构信息

College of Veterinary Medicine, Shandong Agricultural University, Tai'an, Shandong 271018, China.

Research Center for Animal Disease Control Engineering, Shandong Agricultural University, Tai'an, Shandong 271018, China.

出版信息

J Hazard Mater. 2021 May 15;410:124607. doi: 10.1016/j.jhazmat.2020.124607. Epub 2020 Nov 19.

Abstract

Hexavalent chromium (Cr(VI)) is a common heavy metal pollutant in environment and has been proved possessing the cytotoxicity. In this study, we aimed to investigate the role of activating transcription factor 6 (ATF-6) in apoptosis of chicken embryo fibroblasts cell line (DF-1) induced by Cr(VI). Firstly, DF-1 cells were exposed to Cr(VI) to establish the cytotoxicity model, then the cell apoptosis and ATF-6 protein level were analyzed. By silencing ATF-6 gene, changes of the apoptosis rate and apoptotic proteins were examined. To further explore the regulatory mechanism of ATF-6, endoplasmic reticulum (ER) stress, mitochondrial function, reactive oxygen species (ROS) level, as well as the related pathway were evaluated. Results showed that Cr(VI) can result in DF-1 cell apoptosis, along with mitochondrial membrane potential (MMP) reducing and ER stress. Meanwhile, ATF-6 silencing lowered the apoptosis rate and ER stress level, showing with the decrease of XBP-1, PERK, GRP78, Caspase-12, Cleaved Caspase-3 and the increase of Bcl-2. Further analysis found that ATF-6 silencing down-regulated ROS and caused MMP loss, suggesting that ATF-6 silencing inhibited Cr(VI)-induced mitochondrial damage. In conclusion, this study indicate that ATF-6 plays an important regulatory role in Cr(VI)-induced DF-1 cell apoptosis through the ER stress and mitochondrial pathway.

摘要

六价铬(Cr(VI))是环境中常见的重金属污染物,已被证明具有细胞毒性。在这项研究中,我们旨在研究激活转录因子 6(ATF-6)在 Cr(VI)诱导的鸡胚成纤维细胞系(DF-1)细胞凋亡中的作用。首先,将 DF-1 细胞暴露于 Cr(VI)中以建立细胞毒性模型,然后分析细胞凋亡和 ATF-6 蛋白水平。通过沉默 ATF-6 基因,检测细胞凋亡率和凋亡蛋白的变化。为了进一步探讨 ATF-6 的调控机制,评估内质网(ER)应激、线粒体功能、活性氧(ROS)水平以及相关通路。结果表明,Cr(VI)可导致 DF-1 细胞凋亡,同时伴有线粒体膜电位(MMP)降低和 ER 应激。同时,沉默 ATF-6 降低了细胞凋亡率和 ER 应激水平,表现为 XBP-1、PERK、GRP78、Caspase-12、Cleaved Caspase-3 的减少和 Bcl-2 的增加。进一步分析发现,沉默 ATF-6 下调了 ROS 并导致 MMP 丢失,表明沉默 ATF-6 抑制了 Cr(VI)诱导的线粒体损伤。综上所述,本研究表明 ATF-6 通过 ER 应激和线粒体途径在 Cr(VI)诱导的 DF-1 细胞凋亡中发挥重要的调节作用。

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