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Identification of MicroRNAs Involved in Hypoxia- and Serum Deprivation-Induced Apoptosis in Mesenchymal Stem Cells

机译:参与缺氧和血清剥夺诱导的间充质干细胞凋亡的microRNA的鉴定。

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The use of bone marrow mesenchymal stem cell- (MSC) transplantation therapy for cardiac diseases is limited due to poor survival of implanted cells. MicroRNAs (miRNAs) have been reported to be involved in regulating almost all cellular processes, including apoptosis. In this study, we found that the miRNA profile was altered during apoptosis induced by hypoxia and serum deprivation (hypoxia/SD). We further revealed that over-expression of miR-21, miR-23a and miR-210 could promote the survival of MSCs exposed to hypoxia/SD. In contrast, down-regulation of miR-21, miR-23a and miR-503 aggravated apoptosis of MSCs. It was indicated that these miRNAs may play important roles during MSC apoptosis induced by hypoxia/SD.
机译:骨髓间充质干细胞(MSC)移植疗法在心脏病方面的应用受到限制,原因是植入的细胞存活率低。据报道,MicroRNA(miRNA)参与调节几乎所有细胞过程,包括细胞凋亡。在这项研究中,我们发现在低氧和血清剥夺(低氧/ SD)诱导的凋亡过程中,miRNA谱发生了改变。我们进一步揭示,miR-21,miR-23a和miR-210的过度表达可以促进暴露于低氧/ SD的MSC的存活。相反,miR-21,miR-23a和miR-503的下调加重了MSC的凋亡。提示这些miRNA在缺氧/ SD诱导的MSC凋亡中可能起重要作用。

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