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sonic hedgehog 和 Nell-1 信号在人脂肪来源基质细胞成骨分化与成脂分化中的相加效应。

Additive effects of sonic hedgehog and Nell-1 signaling in osteogenic versus adipogenic differentiation of human adipose-derived stromal cells.

机构信息

Section of Orthodontics, Dental and Craniofacial Research Institute, School of Dentistry, University of California, Los Angeles, California, USA.

出版信息

Stem Cells Dev. 2012 Aug 10;21(12):2170-8. doi: 10.1089/scd.2011.0461. Epub 2012 Feb 22.

Abstract

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.

摘要

成骨(骨形成)和脂肪形成(脂肪形成)间充质干细胞(MSC)分化之间存在理论上的反比关系。这种理论上的反比关系部分构成了骨质疏松症的临床实体,其中骨髓间充质干细胞对脂肪分化具有偏好,且这种偏好会随着年龄的增长而增加。最近研究了两种促成骨细胞的细胞因子,它们都具有抗脂肪形成的特性:Sonic Hedgehog(SHH)和 NELL-1 蛋白。在本研究中,我们检测了 SHH 的生物活性 N 端(SHH-N)和 NELL-1 蛋白对人原代脂肪来源基质细胞(hASCs)成骨和脂肪分化的潜在相加作用。我们观察到,重组 SHH-N 和 NELL-1 蛋白均显著增强了所有检测标记物(碱性磷酸酶、茜素红和油红 O 染色和成骨基因表达)的成骨分化并减少了脂肪分化。此外,SHH-N 和 NELL-1 指导的信号通路对 hASCs 的促成骨和抗脂肪分化产生了相加作用。NELL-1 处理增加了 Hedgehog 信号通路的表达;施用 Smoothened 拮抗剂 Cyclopamine 逆转了 NELL-1 的促成骨作用。总之,Hedgehog 和 Nell-1 信号通路对 ASCs 的促成骨和抗脂肪分化具有相加作用。这些研究表明,SHH-N+NELL-1 组合细胞因子可能代表诱导 MSC 成骨分化的可行未来技术。

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