通过ROS介导的PERK-CHOP通路在诱导的HepG2细胞亡中起着重要作用
Cao Zhaohui1,2, Tang Cifei1,2, Huang Di1,2
1Department of Biochemistry and Molecular Biology, School of Basic Medicine, Hengyang Medical School, University of South China, Hengyang, China.
Environmental toxicology
|June 10, 2023
概括
暴露于会通过诱导氧化和内细胞网膜应激引起肝细胞死亡,从而激活特定的亡途径. 针对这些压力可能为引起的肝损伤提供新的治疗策略.
科学领域:
- 肝病学 肝病学是一种肝病学.
- 毒理学 毒理学 毒理学
- 细胞生物学 细胞生物学
背景情况:
- (Cd) 是一种有毒的重金属,已知有肝毒性.
- 由于Cd诱导的肝毒性和亡的确切机制仍然不完全理解.
研究的目的:
- 阐明Cd在HepG2肝细胞中诱导亡的分子机制.
- 调查氧化应激和内细胞网膜 (ER) 应激在Cd诱导的肝毒性中的作用.
主要方法:
- 肝炎G2细胞暴露于.
- 评估了细胞活力,细胞亡,活性氧物种 (ROS) 水平和ER压力标志物 (PERK,CHOP,Ca2+释放).
- 使用N-乙-l-氨酸 (NAC) 作为ROS清理剂.
主要成果:
- 暴露于Cd显著降低了HepG2细胞活力,并增加了细胞亡.
- 通过PERK-CHOP通路增加ROS水平和ER压力,Cd诱导了氧化应激.
- NAC预处理减轻了ER压力并保护了ER功能,表明氧化和ER压力之间存在联系.
结论:
- Cd通过涉及ER应激 (PERK-CHOP轴) 的ROS介导的亡途径诱导HepG2细胞死亡.
- 这项研究揭示了Cd诱导的肝毒性的一种新机制.
- 氧化和ER压力的抑制剂可能代表Cd诱导的肝损伤的治疗方法.
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