一个依赖于的氧化还原静态调节了上皮干细胞的命运
Xi Chen1, Krishnan Raghunathan1, Bin Bao1
1Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital; Harvard Medical School, Boston, MA, USA.
Nature communications
|November 28, 2025
概括
细胞氧化还原平衡整合了利基信号来控制肠干细胞 (ISC) 的命运. 缺氧和Wnt信号调节NADPH氧化酶1 (NOX1),影响ISC代谢和细胞循环进入.
科学领域:
- 细胞生物学 细胞生物学
- 干细胞生物学 干细胞生物学
- 胃肠病学 胃肠病学
背景情况:
- 肠道干细胞 (ISC) 受到微小环境的调节.
- 利基线索,ISC代谢和细胞命运之间的相互作用尚未完全理解.
研究的目的:
- 为了研究细胞氧化还原平衡如何将利基因素与代谢状态相结合,以控制ISC命运.
- 阐明缺氧和Wnt信号影响ISC细胞周期调节的机制.
主要方法:
- 研究了NADPH氧化酶1 (NOX1) 在ISC的作用.
- 分析了缺氧和Wnt信号对NOX1表达和活性的影响.
- 研究了细胞氧化还原状态,缺氧诱导因子1α (HIF-1α) 和异酸盐脱酶1 (IDH1) 活性之间的联系.
主要成果:
- 缺氧和Wnt信号协同地将NOX1限制在密码基础上.
- NOX1保持氧化状态,促进ISC细胞循环的进入.
- 涉及HIF-1α和IDH1的自强化电路调节ISC代谢和氧化还原平衡.
结论:
- 细胞的氧化还原平衡作为一个关键的静态控制ISC代谢和细胞循环.
- 这种机制将环境线索与代谢状态相结合,以控制ISC的自我更新和差异化.
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