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Radiation Induces Apoptosis and Osteogenic Impairment through miR-22-Mediated Intracellular Oxidative Stress in Bone Marrow Mesenchymal Stem Cells

机译:通过MiR-22介导的骨髓间充质干细胞中介导的细胞内氧化应激诱导细胞凋亡和骨质发生损伤

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Bone marrow mesenchymal stem cells (BMSCs) were characterized by their multilineage potential and were involved in both bony and soft tissue repair. Exposure of cells to ionizing radiation (IR) triggers numerous biological reactions, including reactive oxygen species (ROS), cellular apoptosis, and impaired differentiation capacity, while the mechanisms of IR-induced BMSC apoptosis and osteogenic impairment are still unclear. Through a recent study, we found that 6 Gy IR significantly increased the apoptotic ratio and ROS generation, characterized by ROS staining and mean fluorescent intensity. Intervention with antioxidant (NAC) indicated that IR-induced cellular apoptosis was partly due to the accumulation of intracellular ROS. Furthermore, we found that the upregulation of miR-22 in rBMSCs following 6 Gy IR played an important role on the ROS generation and subsequent apoptosis. In addition, we firstly demonstrated that miR-22-mediated ROS accumulation and cell injury had an important regulated role on the osteogenic capacity of BMSCs both in vitro and in vivo. In conclusion, IR-induced overexpression of miR-22 regulated the cell viability and differentiation potential through targeting the intracellular ROS.
机译:骨髓间充质干细胞(BMSCs)的特征在于它们的多线粒潜力,并参与骨骼和软组织修复。暴露细胞以电离辐射(IR)触发许多生物反应,包括反应性氧物质(ROS),细胞凋亡和分化能力受损,而IR诱导的BMSC细胞凋亡和成骨损伤的机制仍不清楚。通过最近的研究,我们发现6 Gy IR显着增加了凋亡比和ROS产生,其特征在于ROS染色和平均荧光强度。用抗氧化剂(NAC)的干预表明,IR诱导的细胞凋亡部分是由于细胞内RO的积累。此外,我们发现,在6 Gy IR之后的RBMSC中MIR-22的上调在ROS生成和随后的细胞凋亡中起重要作用。此外,我们首先展示了MiR-22介导的ROS积累和细胞损伤对体外和体内BMSCs的成沸容量具有重要的规范作用。总之,MiR-22的IR诱导过表达通过靶向细胞内RO来调节细胞活力和分化电位。

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