黑色素通过NOTCH1-NRF2-FOXO1-GSH通路†调节子宫内膜分泌
Shan Jin1,2, Ting-Ting Wang1, Ji-Cheng Huang1
1College of Veterinary Medicine, Jilin University, Changchun, P. R. China.
Biology of reproduction
|June 19, 2023
概括
黑色素通过抑制通过MTNR1B受体的树皮细胞分化,损害了人类子宫内膜的分离. 这涉及NOTCH1-NRF2-FOXO1-GSH通路,导致氧化应激和降低谷氨水平.
科学领域:
- 生殖生物学 生殖生物学
- 细胞和分子内分泌学细胞和分子内分泌学.
背景情况:
- 黑色素对于早期的生殖活动至关重要.
- 它在子宫内膜脱细胞化中的作用在很大程度上仍未被探索.
研究的目的:
- 为了研究黑激素对人类子宫内膜层细胞 (ESC) 不同化的作用.
- 阐明黑色素在决定化中的作用背后的分子机制.
主要方法:
- 人类ESCs被用黑激素治疗.
- 评估了关键蛋白质 (NOTCH1,RBPJ,NRF2,FOXO1) 和细胞分化标记物的表达.
- 使用了复合NOTCH1蛋白和途径抑制剂 (DAPT).
- 测量了氧化应激标志物 (ROS,GSH) 和酶活性.
主要成果:
- 黑色素抑制ESC分化和细胞周期进展,但不影响增殖.
- 黑色素降低了NOTCH1,RBPJ,NRF2和FOXO1的表达.
- 黑色素诱导氧化应激,降低谷氨水平和相关的酶活动.
- NOTCH1补充剂抵消了黑激素的抑制作用,而NRF2和FOXO1阻塞加剧了它们.
- 补充GSH可以挽救差异化缺陷.
结论:
- 黑色素通过抑制ESC通过MTNR1B受体的分化,损害子宫内膜分泌.
- 该机制涉及NOTCH1-NRF2-FOXO1-GSH通路,导致氧化应激.
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