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神经上皮细胞样分子1(Nell1)受骨形态发生蛋白9(BMP9)调控,并在间充质干细胞中以牺牲脂肪生成的代价增强BMP9诱导的成骨分化。

NEL-Like Molecule-1 (Nell1) Is Regulated by Bone Morphogenetic Protein 9 (BMP9) and Potentiates BMP9-Induced Osteogenic Differentiation at the Expense of Adipogenesis in Mesenchymal Stem Cells.

作者信息

Wang Jing, Liao Junyi, Zhang Fugui, Song Dongzhe, Lu Minpeng, Liu Jianxiang, Wei Qiang, Tang Shengli, Liu Hao, Fan Jiaming, Zou Yulong, Guo Dan, Huang Jiayi, Liu Feng, Ma Chao, Hu Xue, Li Li, Qu Xiangyang, Chen Liqun, Weng Yaguang, Lee Michael J, He Tong-Chuan, Reid Russell R, Zhang Jiye

出版信息

Cell Physiol Biochem. 2017;41(2):484-500. doi: 10.1159/000456885. Epub 2017 Jan 30.

Abstract

BACKGROUND

BMP9 induces both osteogenic and adipogenic differentiation of mesenchymal stem cells (MSCs). Nell1 is a secretory glycoprotein with osteoinductive and anti-adipogenic activities. We investigated the role of Nell1 in BMP9-induced osteogenesis and adipogenesis in MSCs.

METHODS

Previously characterized MSCs iMEFs were used. Overexpression of BMP9 and NELL1 or silencing of mouse Nell1 was mediated by adenoviral vectors. Early and late osteogenic and adipogenic markers were assessed by staining techniques and qPCR analysis. In vivo activity was assessed in an ectopic bone formation model of athymic mice.

RESULTS

We demonstrate that Nell1 expression was up-regulated by BMP9. Exogenous Nell1 potentiated BMP9-induced late stage osteogenic differentiation while inhibiting the early osteogenic marker. Forced Nell1 expression enhanced BMP9-induced osteogenic regulators/markers and inhibited BMP9-upregulated expression of adipogenic regulators/markers in MSCs. In vivo ectopic bone formation assay showed that exogenous Nell1 expression enhanced mineralization and maturity of BMP9-induced bone formation, while inhibiting BMP9-induced adipogenesis. Conversely, silencing Nell1 expression in BMP9-stimulated MSCs led to forming immature chondroid-like matrix.

CONCLUSION

Our findings indicate that Nell1 can be up-regulated by BMP9, which in turn accelerates and augments BMP9-induced osteogenesis. Exogenous Nell1 may be exploited to enhance BMP9-induced bone formation while overcoming BMP9-induced adipogenesis in regenerative medicine.

摘要

背景

骨形态发生蛋白9(BMP9)可诱导间充质干细胞(MSC)向成骨细胞和脂肪细胞分化。Nell1是一种具有骨诱导和抗脂肪生成活性的分泌性糖蛋白。我们研究了Nell1在BMP9诱导的MSC成骨和脂肪生成中的作用。

方法

使用先前鉴定的MSC iMEF。通过腺病毒载体介导BMP9和NELL1的过表达或小鼠Nell1的沉默。通过染色技术和qPCR分析评估早期和晚期成骨和脂肪生成标志物。在无胸腺小鼠的异位骨形成模型中评估体内活性。

结果

我们证明Nell1表达受BMP9上调。外源性Nell1增强了BMP9诱导的晚期成骨分化,同时抑制了早期成骨标志物。强制表达Nell1增强了BMP9诱导的成骨调节因子/标志物,并抑制了BMP9上调的MSC中脂肪生成调节因子/标志物的表达。体内异位骨形成试验表明,外源性Nell1表达增强了BMP9诱导的骨形成的矿化和成熟,同时抑制了BMP9诱导的脂肪生成。相反,在BMP9刺激的MSC中沉默Nell1表达导致形成不成熟的类软骨样基质。

结论

我们的研究结果表明,Nell1可被BMP9上调,进而加速和增强BMP9诱导的成骨作用。在再生医学中,外源性Nell1可用于增强BMP9诱导的骨形成,同时克服BMP9诱导的脂肪生成。

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