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Role of microRNA-129-5p in osteoblast differentiation from bone marrow mesenchymal stem cells

机译:microRNA-129-5p在骨髓间充质干细胞向成骨细胞分化中的作用

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摘要

Mesenchymal stem cells derived from bone marrow have the capacity to differentiate into osteoblast, chondrocyte, nerve cell and myocardial cell in vitro, which are an ideal engraft in tissue-engineered repair. Osteoblast differentiation is a vital process in maintaining bone homeostasis in which various transcriptional factors, including signaling molecules, and microRNAs (miRNAs). In this research, human bone marrow mesenchymal stem cells (hBMSCs) were induced differentiation into osteoblast in vitro after over-expression of miR-129-5p. The results showed that the hBMSCs could induce differentiation into osteoblast under the special condition medium, but when the miR-129-5p was over-expressed in hBMSCs, the differentiated efficiency and induced time of osteoblast from hBMSCs could be promoted. This reason was demonstrated that signal transducer and activator of transcription 1 (STAT1) was a transcriptional repressor of osteoblast gene (Runx 2) expression during osteoblast differentiation, miR-129-5p reduced STAT1 levels, leading to the accumulation of correctly spliced Runx 2 mRNA and a dramatic increase in Runx 2 protein.
机译:源自骨髓的间充质干细胞具有体外分化为成骨细胞,软骨细胞,神经细胞和心肌细胞的能力,是组织工程修复的理想植入物。成骨细胞的分化是维持骨骼稳态的重要过程,在该过程中,各种转录因子(包括信号分子和microRNA(miRNA))得以保持。在这项研究中,人类骨髓间充质干细胞(hBMSCs)在miR-129-5p过度表达后体外诱导分化为成骨细胞。结果表明,在特殊条件下,hBMSCs可以诱导成骨细胞分化,但是当miR-129-5p在hBMSCs中过表达时,可以促进hBMSCs向成骨细胞的分化效率和诱导时间。此原因表明,信号转导和转录激活因子1(STAT1)是成骨细胞分化过程中成骨细胞基因(Runx 2)表达的转录抑制因子,miR-129-5p降低STAT1水平,导致正确剪接的Runx 2 mRNA积累以及Runx 2蛋白的急剧增加。

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