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Reactive Oxygen Species Are Required for Human Mesenchymal Stem Cells to Initiate Proliferation after the Quiescence Exit

机译:人间充质干细胞在退出静止状态后开始增殖时需要活性氧

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The present study focuses on the involvement of reactive oxygen species (ROS) in the process of mesenchymal stem cells “waking up” and entering the cell cycle after the quiescence. Using human endometrial mesenchymal stem cells (eMSCs), we showed that intracellular basal ROS level is positively correlated with the proliferative status of the cell cultures. Our experiments with the eMSCs synchronized in the G0phase of the cell cycle revealed a transient increase in the ROS level upon the quiescence exit after stimulation of the cell proliferation. This increase was registered before the eMSC entry to the S-phase of the cell cycle, and elimination of this increase by antioxidants (N-acetyl-L-cysteine, Tempol, and Resveratrol) blocked G1–S-phase transition. Similarly, a cell cycle arrest which resulted from the antioxidant treatment was observed in the experiments with synchronized human mesenchymal stem cells derived from the adipose tissue. Thus, we showed that physiologically relevant level of ROS is required for the initiation of human mesenchymal stem cell proliferation and that low levels of ROS due to the antioxidant treatment can block the stem cell self-renewal.
机译:本研究的重点是活性氧(ROS)参与间充质干细胞“唤醒”并在静止后进入细胞周期的过程。使用人子宫内膜间充质干细胞(eMSCs),我们显示细胞内的基础ROS水平与细胞培养物的增殖状态正相关。我们在细胞周期的G0期同步化的eMSC的实验表明,刺激细胞增殖后,在静止退出时,ROS水平会瞬时升高。这种增加在eMSC进入细胞周期的S期之前就已经被记录下来,并且抗氧化剂(N-乙酰基-L-半胱氨酸,Tempol和白藜芦醇)消除了这种增加,从而阻止了G1-S期的转变。类似地,在实验中观察到由抗脂肪处理导致的细胞周期停滞,所述同步化的人间充质干细胞来源于脂肪组织。因此,我们表明启动人间充质干细胞增殖需要生理相关水平的ROS,并且由于抗氧化剂处理而导致的低水平ROS可以阻止干细胞的自我更新。

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