PPARα感知双S触发EP300介导的自阻塞和肝硬化症
Jingjia Liang1,2, Cheng Xu1,2, Jin Xu1,2,3
1State Key Laboratory of Reproductive Medicine and Offspring Health, School of Public Health, Nanjing Medical University, Nanjing 211166, China.
Environmental science & technology
|December 12, 2023
概括
双S (BPS) 暴露与非酒精性肝病 (NAFLD) 风险增加有关. 通过影响EP300,BPS破坏肝脏自,导致脂质积累和NAFLD的发展.
科学领域:
- 环境健康 环境健康
- 毒理学 毒理学 毒理学
- 肝病学 肝病学是一种肝病学.
背景情况:
- 双S (BPS) 越来越多地被用作BPA的替代品,引发了人们对其健康影响的担忧.
- BPS暴露与非酒精性肝病 (NAFLD) 和其潜在机制之间的关联尚未得到充分理解.
研究的目的:
- 研究人类群体中BPS暴露和NAFLD之间的相关性.
- 阐明BPS导致NAFLD的分子机制,重点关注肝脏自.
主要方法:
- 在中国和美国队列中分析了BPS水平 (血清和尿液) 和NAFLD患病率.
- 利用小鼠模型研究BPS暴露对肝脂积累和自的影响.
- 研究了EP300,PPARα和mTORC1信号在BPS诱导的NAFLD中的作用.
主要成果:
- 血清和尿液中BPS水平的升高与这两种人群中NAFLD风险的增加显著相关.
- 在小鼠中,BPS暴露导致肝脏脂质积累和自功能受损.
- BPS通过PPARα激活EP300表达,促进EP300转位和Raptor乙化,从而抑制自和脂质降解.
结论:
- 暴露于BPS是NAFLD的一个危险因素.
- 通过阻断肝脏自,EP300是BPS诱导的NAFLD发展的关键调解者.
- 这项研究为BPS对肝脏健康的毒性机制提供了新的见解.
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