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IGF1 potentiates BMP9-induced osteogenic differentiation in mesenchymal stem cells through the enhancement of BMP/Smad signaling

机译:IGF1通过增强BMP / SMAD信号传导,增强BMP9诱导的间充质干细胞的骨质发生分化

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Engineered bone tissue is thought to be the ideal alternative for bone grafts in the treatment of related bone diseases. BMP9 has been demonstrated as one of the most osteogenic factors, and enhancement of BMP9-induced osteogenesis will greatly accelerate the development of bone tissue engineering. Here, we investigated the effect of insulin-like growth factor 1 (IGF1) on BMP9-induced osteogenic differentiation, and unveiled a possible molecular mechanism underling this process. We found that IGF1 and BMP9 are both detectable in mesenchymal stem cells (MSCs). Exogenous expression of IGF1 potentiates BMP9-induced alkaline phosphatase (ALP), matrix mineralization, and ectopic bone formation. Similarly, IGF1 enhances BMP9-induced endochondral ossification. Mechanistically, we found that IGF1 increases BMP9-induced activation of BMP/Smad signaling in MSCs. Our findings demonstrate that IGF1 can enhance BMP9-induced osteogenic differentiation in MSCs, and that this effect may be mediated by the enhancement of the BMP/Smad signaling transduction triggered by BMP9.
机译:被设计成型骨组织是骨移植治疗相关骨病的理想选择。 BMP9已被证明是最易造成的因素之一,BMP9诱导的成骨的增强将极大地加速骨组织工程的发展。在这里,我们研究了胰岛素样生长因子1(IGF1)对BMP9诱导的骨质发生分化的影响,并推出了该方法的可能分子机制。我们发现IGF1和BMP9在间充质干细胞(MSC)中均可检测。 IGF1促高素质的外源表达BMP9诱导碱性磷酸酶(ALP),基质矿化和异位骨形成。同样,IGF1增强了BMP9诱导的endochondrall骨化。机械地,我们发现IGF1增加了MSCS中BMP9诱导的BMP / Smad信号的激活。我们的研究结果表明,IGF1可以增强BMP9诱导的MSC中的骨质分化,并且这种效果可以通过BMP9触发的BMP / Smad信号转导的增强来介导。

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