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MiR-637 maintains the balance between adipocytes and osteoblasts by directly targeting Osterix

机译:MiR-637通过直接靶向Osterix来维持脂肪细胞和成骨细胞之间的平衡

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摘要

Bone development is dynamically regulated by homeostasis, in which a balance between adipocytes and osteoblasts is maintained. Disruption of this differentiation balance leads to various bone-related metabolic diseases, including osteoporosis. In the present study, a primate-specific microRNA (miR-637) was found to be involved in the differentiation of human mesenchymal stem cells (hMSCs). Our preliminary data indicated that miR-637 suppressed the growth of hMSCs and induced S-phase arrest. Expression of miR-637 was increased during adipocyte differentiation (AD), whereas it was decreased during osteoblast differentiation (OS), which suggests miR-637 could act as a mediator of adipoosteogenic differentiation. Osterix (Osx), a significant transcription factor of osteoblasts, was shown to be a direct target of miR-637, which significantly enhanced AD and suppressed OS in hMSCs through direct suppression of Osx expression. Furthermore, miR-637 also significantly enhanced de novo adipogenesis in nude mice. In conclusion, our data indicated that the expression of miR-637 was indispensable for maintaining the balance of adipocytes and osteoblasts. Disruption of miR-637 expression patterns leads to irreversible damage to the balance of differentiation in bone marrow.
机译:体内平衡动态调节骨骼的发育,其中脂肪细胞和成骨细胞之间的平衡得以维持。这种分化平衡的破坏导致各种与骨有关的代谢疾病,包括骨质疏松症。在本研究中,发现灵长类特异性microRNA(miR-637)参与人间充质干细胞(hMSCs)的分化。我们的初步数据表明,miR-637抑制hMSC的生长并诱导S期阻滞。 miR-637的表达在脂肪细胞分化(AD)的过程中增加,而在成骨细胞分化(OS)的过程中降低,这表明miR-637可以作为脂肪成骨分化的媒介。 Osterix(Osx)是成骨细胞的重要转录因子,被证明是miR-637的直接靶标,它可以通过直接抑制Osx表达来显着增强hMSC中的AD并抑制OS。此外,miR-637还显着增强了裸鼠的新生脂肪形成。总之,我们的数据表明,miR-637的表达对于维持脂肪细胞和成骨细胞的平衡是必不可少的。 miR-637表达模式的破坏导致骨髓分化平衡不可逆转的破坏。

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