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Dysregulation of the miR-146a-Smad4 axis impairs osteogenesis of bone mesenchymal stem cells under inflammation

机译:miR-146a-Smad4轴失调损害炎症下骨间充质干细胞的成骨作用

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摘要

Osteoporosis is a common disease that affects patient quality of life, especially among the elderly population. Although inflammation contributes significantly to osteoporosis, the underlying mechanism is unclear. In this study, we found that tumor necrosis factor (TNF)-α, an inflammatory environment mimic, inhibits osteogenesis of bone mesenchymal stem cells (BMSCs), induces miR-146a and decreases Smad4. Moreover, overexpression of miR-146a inhibited the osteogenic ability of BMSCs, whereas blocking miR-146a partially rescued the osteogenesis deficiency under TNF-α treatment. Molecularly, miR-146a decreased Smad4 expression at the protein level by binding to an element located in the Smad4 3′-untranslated region, and restoration of Smad4 reversed the inhibitory effects of miR-146a on osteogenesis. Together, our results showed that the inflammatory environment mimic TNF-α inhibits osteogenesis via upregulation of miR-146a and subsequent downregulation of Smad4, thus suggesting that therapeutic manipulation of miR-146a maybe a potential strategy to improve osteogenesis in the context of osteoporosis.
机译:骨质疏松症是一种常见的疾病,会影响患者的生活质量,尤其是在老年人口中。尽管炎症是导致骨质疏松的重要原因,但其潜在机制尚不清楚。在这项研究中,我们发现肿瘤坏死因子(TNF)-α,一种炎性环境模拟物,抑制骨间充质干细胞(BMSCs)的成骨作用,诱导miR-146a并降低Smad4。此外,miR-146a的过表达抑制了骨髓间充质干细胞的成骨能力,而阻断miR-146a在TNF-α处理下部分挽救了成骨缺陷。在分子上,miR-146a通过与位于Smad4 3'-非翻译区的元件结合而在蛋白质水平上降低Smad4表达,并且Smad4的还​​原逆转了miR-146a对成骨的抑制作用。总之,我们的研究结果表明,模仿TNF-α的炎性环境通过miR-146a的上调和随后Smad4的下调来抑制成骨作用,因此表明miR-146a的治疗性操作可能是改善骨质疏松情况下成骨作用的潜在策略。

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