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首页> 外文期刊>Stem cells and development >Additive effects of sonic hedgehog and nell-1 signaling in osteogenic versus adipogenic differentiation of human adipose-derived stromal cells
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Additive effects of sonic hedgehog and nell-1 signaling in osteogenic versus adipogenic differentiation of human adipose-derived stromal cells

机译:刺猬和nell-1信号传导在人类脂肪基质细胞成骨和成脂分化中的累加作用

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A theoretical inverse relationship exists between osteogenic (bone forming) and adipogenic (fat forming) mesenchymal stem cell (MSC) differentiation. This inverse relationship in theory partially underlies the clinical entity of osteoporosis, in which marrow MSCs have a preference for adipose differentiation that increases with age. Two pro-osteogenic cytokines have been recently studied that each also possesses antiadipogenic properties: Sonic Hedgehog (SHH) and NELL-1 proteins. In the present study, we assayed the potential additive effects of the biologically active N-terminus of SHH (SHH-N) and NELL-1 protein on osteogenic and adipogenic differentiation of human primary adipose-derived stromal cell (hASCs). We observed that both recombinant SHH-N and NELL-1 protein significantly enhanced osteogenic differentiation and reduced adipose differentiation across all markers examined (alkaline phosphatase, Alizarin red and Oil red O staining, and osteogenic gene expression). Moreover, SHH-N and NELL-1 directed signaling produced additive effects on the pro-osteogenic and antiadipogenic differentiation of hASCs. NELL-1 treatment increased Hedgehog signaling pathway expression; coapplication of the Smoothened antagonist Cyclopamine reversed the pro-osteogenic effect of NELL-1. In summary, Hedgehog and Nell-1 signaling exert additive effects on the pro-osteogenic and antiadipogenic differentiation of ASCs. These studies suggest that the combination cytokines SHH-N+NELL-1 may represent a viable future technique for inducing the osteogenic differentiation of MSCs.
机译:成骨(成骨)和成脂(成脂)间充质干细胞(MSC)分化之间存在理论上的逆向关系。从理论上说,这种反比关系部分地是骨质疏松症临床实体的基础,其中骨髓MSC倾向于随着年龄增长而脂肪分化。最近研究了两种促成骨细胞因子,每种还具有抗脂肪形成特性:声波刺猬(SHH)和NELL-1蛋白。在本研究中,我们分析了SHH(SHH-N)和NELL-1蛋白的生物活性N末端对人原发性脂肪基质细胞(hASCs)成骨和成脂分化的潜在累加作用。我们观察到,重组SHH-N和NELL-1蛋白在所有检查的标志物(碱性磷酸酶,茜素红和油红O染色以及成骨基因表达)上均显着增强了成骨分化并降低了脂肪分化。此外,SHH-N和NELL-1定向信号传导对hASC的促成骨和抗脂肪形成分化产生累加效应。 NELL-1处理可增加刺猬信号通路的表达;平滑拮抗剂拮抗剂环丙胺的共同应用逆转了NELL-1的促成骨作用。总之,Hedgehog和Nell-1信号传导对ASC的促成骨和抗脂肪形成分化产生附加作用。这些研究表明,细胞因子SHH-N + NELL-1的组合可能代表了诱导MSCs成骨分化的可行的未来技术。

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