通过通过Trim25/Keap1/Nrf2轴抑制内质网膜应激,EETs可以缓解膜上皮细胞衰老
Chen-Yu Zhang1, Wen-Jing Zhong1, Yu-Biao Liu1
1Department of Physiology, School of Basic Medicine Science, Central South University, Changsha, Hunan, 410078, China.
环氧乙酸 (EETs) 可以缓解膜上皮细胞 (AEC) 衰老,这是慢性肺部疾病的关键因素. 增加EETs水平为肺部疾病治疗提供了新的治疗目标.
科学领域:
- 细胞衰老 细胞衰老
- 慢性肺部疾病 慢性肺部疾病
- 老龄化的分子机制.
背景情况:
- 膜上皮细胞 (AEC) 衰老驱动慢性肺部疾病.
- 需要有效的策略来缓解AEC衰老.
- 环氧乙酸 (EETs) 是细胞衰老的潜在调节者.
研究的目的:
- 调查EETs在缓解AEC衰老中的作用.
- 阐明EETs影响AEC衰老的分子机制.
- 评估EETs在早衰老小鼠模型中的治疗潜力.
主要方法:
- 使用衰老的AEC进行体外研究.
- 补充外源EETs,过度表达CYP2J2和抑制可溶性环氧化酶 (sEH).
- 在体内研究使用D-银糖诱导过早衰老的小鼠模型,用sEH抑制剂 (TPPU) 治疗.
主要成果:
- 14,15-EET水平在老化的AEC下降.
- 服用ET补充剂,过度表达CYP2J2和抑制SEH可以缓解AEC衰老.
- 14,15-EET促进了Trim25的表达,导致Keap1降解和Nrf2核转位以产生抗氧化作用.
- 在老年小鼠中,TPPU治疗减少了衰老标志物 (p16,p21,γH2AX) 和肺纤维化.
结论:
- EETs是AECs的新型抗衰老物质.
- 准EETs代谢为慢性肺部疾病提供了一个新的治疗策略.
- EETs-Nrf2通路对于抑制内质网膜应激和AEC衰老至关重要.
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