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Dynamic changes in intracellular ROS levels regulate airway basal stem cell homeostasis through Nrf2-dependent notch signaling

机译:细胞内ROS水平的动态变化通过依赖于Nrf2的Notch信号调节气道基底干细胞稳态

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摘要

Airways are exposed to myriad environmental and damaging agents such as reactive oxygen species (ROS), which also have physiological roles as signaling molecules that regulate stem cell function. However, the functional significance of both steady and dynamically changing ROS levels in different stem cell populations, as well as downstream mechanisms that integrate ROS sensing into decisions regarding stem cell homeostasis, are unclear. Here, we show in mouse and human airway basal stem cells (ABSCs) that intracellular flux from low to moderate ROS levels is required for stem cell self-renewal and proliferation. Changing ROS levels activate Nrf2, which activates the Notch pathway to stimulate ABSC self-renewal and an antioxidant program that scavenges intracellular ROS, returning overall ROS levels to a low state to maintain homeostatic balance. This redox-mediated regulation of lung stem cell function has significant implications for stem cell biology, repair of lung injuries, and diseases such as cancer.
机译:气道暴露于多种环境和破坏性物质,例如活性氧(ROS),它们也具有生理作用,作为调节干细胞功能的信号分子。然而,尚不清楚在不同干细胞群体中稳定且动态变化的ROS水平的功能意义,以及将ROS传感整合到有关干细胞稳态决策中的下游机制。在这里,我们在小鼠和人气道基底干细胞(ABSCs)中显示,从低到中等ROS水平的细胞内通量对于干细胞自我更新和增殖是必需的。不断变化的ROS水平激活Nrf2,后者激活Notch途径以刺激ABSC自我更新,并产生抗氧化剂程序,清除细胞内ROS,使总ROS水平恢复至低水平以保持体内平衡。氧化还原介导的肺干细胞功能调节对干细胞生物学,肺损伤修复和癌症等疾病具有重要意义。

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