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首页> 外文期刊>Experimental Biology and Medicine: Journal of the Society for Experimental Biology and Medicine >MiR-145 regulates osteogenic differentiation of human adipose-derived mesenchymal stem cells through targeting FoxO1
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MiR-145 regulates osteogenic differentiation of human adipose-derived mesenchymal stem cells through targeting FoxO1

机译:MiR-145通过靶向FoxO1调节人脂肪衍生的间充质干细胞的成骨分化

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摘要

In this study, we aimed to investigate the expression of miR-145 before and after hASCs osteogenic differentiation. We also intended to explore the influence of the target relationship between miR-145 and FoxO1 on osteogenic differentiation. Dual-luciferase reporter gene assay and real-time PCR were used to confirm the target relationship between miR-145 and FoxO1. Furthermore, the modulatory effects of miR-145 and FoxO1 on hASCs osteoinductive differentiation were measured by real-time PCR , Western blot, ALP staining, ARS staining, and cell immunofluorescence assay. After osteogenic differentiation, miR-145 was gradually down-regulated, while FoxO1 was up-regulated in hASCs. MiR-145 could directly target FoxO1 3UTR. FoxO1 was negatively regulated by miR-145. After osteoinductive differentiation, BSP, Ocn, and OPN expression was lowered with the overexpression of miR-145 or the knockdown of FoxO1. Furthermore, ALP and ARS staining assay results showed weakened ALP activity and extracellular matrix calcification. When overexpressing miR-145 and FoxO1 simultaneously, no obvious change in ALP activity and extracellular matrix calcification was seen. MiR-145 could suppress hASCs osteoinductive differentiation by suppressing FoxO1 directly.
机译:在这项研究中,我们旨在探讨Hascs oSteogenic分化前后miR-145的表达。我们还旨在探讨MIR-145和FOXO1对成骨分化的目标关系的影响。双荧光素酶报告基因测定和实时PCR用于确认miR-145和FoxO1之间的靶标关系。此外,通过实时PCR,Western印迹,ALP染色,ARS染色和细胞免疫荧光测定,测量miR-145和FoxO1对HASCS骨诱导分化的调节效果。在成骨分化后,miR-145逐渐下调,而FOXO1在HASC中上调。 MiR-145可以直接针对FoxO1 3UTR。 FOXO1受MIR-145负调节。骨诱导分化后,用MiR-145的过表达或FoxO1的敲低降低BSP,OCN和OPN表达。此外,ALP和ARS染色测定结果显示出弱化ALP活性和细胞外基质钙化。同时过度表达MIR-145和FOXO1时,没有看到ALP活性和细胞外基质钙化的明显变化。 MiR-145可以通过直接抑制FoxO1来抑制Hascs骨诱导性分化。

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