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首页> 外文期刊>Bone >Administration of tauroursodeoxycholic acid enhances osteogenic differentiation of bone marrow-derived mesenchymal stem cells and bone regeneration
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Administration of tauroursodeoxycholic acid enhances osteogenic differentiation of bone marrow-derived mesenchymal stem cells and bone regeneration

机译:TaursoSoxicholic酸的施用增强了骨髓衍生的间充质干细胞和骨再生的成骨分化

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It is known that osteogenic differentiation of mesenchymal stem cells (MSCs) can be promoted by suppression of adipogenesis of MSCs. We have recently found that the chemical chaperone tauroursodeoxycholic acid (TUDCA) significantly reduces adipogenesis of MSCs. In the present study, we examined whether TUDCA can promote osteogenic differentiation of bone marrow-derived mesenchymal stem cells (BMMSCs) by regulating Integrin 5 (ITGA5) associated with activation of ERK1/2 signal pathway and thereby enhance bone tissue regeneration by reducing apoptosis and the inflammatory response. TUDCA treatment promoted in vitro osteogenic differentiation of BMMSCs and in vivo bone tissue regeneration in a calvarial defect model, as confirmed by micro computed tomography, histological staining, and immunohistochemistry for osteocalcin. In addition, TUDCA treatment significantly decreased apoptosis and the inflammatory response in vivo and in vitro, which is important to enhance bone tissue regeneration. These results indicate that TUDCA plays a critical role in enhancing osteogenesis of BMMSCs, and is therefore a potential alternative drug for bone tissue regeneration. (c) 2015 Elsevier Inc. All rights reserved.
机译:众所周知,通过抑制MSCs的脂肪发生,可以促进间充质干细胞(MSCs)的成骨分化。我们最近发现化学伴侣Tauroursodoxycholic酸(Tudca)显着降低了MSCs的脂肪生成。在本研究中,我们检查了TUDCA是否可以通过调节与激活ERK1 / 2信号途径的激活相关的整联蛋白5(ITGA5)来促进骨髓衍生的间充质干细胞(BMMSC)的骨质分化,从而通过减少细胞凋亡和增强骨组织再生炎症反应。 Tudca治疗促进了BMMSCs的体外骨质发生分化,并在颅骨缺陷模型中进行了体内骨组织再生,如微型计算机断层扫描,组织学染色和骨癌免疫组织化学证实。此外,Tudca治疗显着降低了体内和体外炎症反应,这对于增强骨组织再生是重要的。这些结果表明,TUDCA在增强BMMSC的成骨方面发挥着关键作用,因此是骨组织再生的潜在替代药物。 (c)2015 Elsevier Inc.保留所有权利。

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