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首页> 外文期刊>Frontiers in Molecular Biosciences >ZEB1 Mediates Bone Marrow Mesenchymal Stem Cell Osteogenic Differentiation Partly via Wnt/β-Catenin Signaling
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ZEB1 Mediates Bone Marrow Mesenchymal Stem Cell Osteogenic Differentiation Partly via Wnt/β-Catenin Signaling

机译:Zeb1部分通过Wnt /β-catenin信号传导介导骨髓间充质干细胞骨质骨质分化

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Abstract ZEB1 is zinc-finger transcription factors best known for its role in promoting epithelial-mesenchymal transition, which is also related to osteogenesis. In present study, ZEB1 was investigated for its involvement in osteoblasts commitment of BMSCs. ZEB1 was confirmed its expression decreased following osteogenic differentiation. In vitro, Silencing of ZEB1 in BMSCs promoted osteogenic activity and mineralization, vice versa. The increase of osteogenic differentiation induced by si-ZEB1 could be partly rescued by inhibitor of Wnt/β-catenin (si-β-catenin). In vivo, knockdown of ZEB1 in BMSCs inhibited the rapid bone loss of OVX mice. It was also proven that the expression of ZEB1 negatively associated with bone mass and bone formation in postmenopausal patients. In conclusion, ZEB1 was an essential transcription factor in BMSCs differentiation and may serve as a potential anabolic strategy for treatment and prevention of postmenopausal osteoporosis.
机译:摘要Zeb1是锌指转录因子,其作用在促进上皮 - 间充质转化中,这也与骨发生有关。 在目前的研究中,研究了Zeb1的参与BMSCs的成骨细胞承诺。 Zeb1被证实了其表达后骨质发生分化后的表达降低。 体外,BMSCS中Zeb1的沉默促进了成骨活性和矿化,反之亦然。 通过Wnt /β-catenin(Si-β-catenin)的抑制剂可以部分地抵抗Si-Zeb1诱导的骨质发生分化的增加。 在体内,BMSCS中Zeb1的敲低抑制了OVX小鼠的快速骨质损失。 还证实,绝经后患者在绝经后患者中与骨质和骨骼形成负相关的Zeb1的表达。 总之,Zeb1是BMSCS分化中的基本转录因子,可以作为治疗和预防绝经后骨质疏松症的潜在合成代谢策略。

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