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首页> 外文期刊>The Journal of biological chemistry >Control of Mesenchymal Lineage Progression by MicroRNAs Targeting Skeletal Gene Regulators Trps1 and Runx2
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Control of Mesenchymal Lineage Progression by MicroRNAs Targeting Skeletal Gene Regulators Trps1 and Runx2

机译:用Micrornas靶向骨骼基因调节器TRPS1和RUNX2的间充质谱系进展

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Multiple microRNAs (miRNAs) that target the osteogenic Runt-related transcription factor 2 (RUNX2) define an interrelated network of miRNAs that control osteoblastogenesis. We addressed whether these miRNAs have functional targets beyond RUNX2 that coregulate skeletal development. Here, we find that seven RUNX2-targeting miRNAs (miR-23a, miR-30c, miR-34c, miR-133a, miR-135a, miR-205, and miR-217) also regulate the chondrogenic GATA transcription factor tricho-rhino-phalangeal syndrome I (TRPS1). Although the efficacy of each miRNA to target RUNX2 or TRPS1 differs in osteoblasts and chondrocytes, each effectively blocks maturation of precommitted osteoblasts and chondrocytes. Furthermore, these miRNAs can redirect mesenchymal stem cells into adipogenic cell fate with concomitant up-regulation of key lineage-specific transcription factors. Thus, a program of multiple miRNAs controls mesenchymal lineage progression by selectively blocking differentiation of osteoblasts and chondrocytes to control skeletal development.
机译:靶向成骨的runt相关转录因子2(RUNX2)的多个microRNAs(miRNA)限定了控制骨菌细胞发生的密族的相互关联的网络。我们解决这些MIRNA是否具有超越Runx2的功能目标,该目标是Coregulate骨骼发育。在这里,我们发现七个runx2靶向miRNA(miR-23a,miR-30c,miR-34c,miR-133a,miR-135a,miR-205和miR-217)还调节软骨内的Gata转录因子Tricho-r​​hino -Phalangeal综合症I(TRPS1)。虽然每个miRNA对靶Runx2或TRPS1的疗效不同,但是骨细胞和软骨细胞的不同之处在于,各自有效地阻断了预切片的成骨细胞和软骨细胞的成熟。此外,这些miRNA可以通过伴随关键谱系特异性转录因子来将间充质干细胞重定向到adipogenic细胞命运中。因此,多种miRNA的程序通过选择性地阻断成骨细胞和软骨细胞的分化来控制间充质谱系进展,以控制骨骼发育。

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