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NT-3 通过调节 Akt 通路促进小鼠骨髓间充质干细胞的成骨分化。

NT-3 promotes osteogenic differentiation of mouse bone marrow mesenchymal stem cells by regulating the Akt pathway.

机构信息

Medical Research Center, Yue Bei People's Hospital Affiliated to Shantou University Medical College, P.R. China.

Department of Anatomy, Qiqihar Medical University, P.R. China.

出版信息

J Musculoskelet Neuronal Interact. 2020 Dec 1;20(4):591-599.

Abstract

OBJECTIVES

To investigate the effect of neurotrophin-3 (NT-3) on osteogenic/adipogenic differentiation of bone marrow mesenchymal stem cells (BMSCs).

METHODS

Osteogenic differentiation was detected by alkaline phosphatase (ALP) staining and alizarin red staining (ARS). Adipogenic differentiation was detected by oil red O (ORO) staining. The expression of bone-related genes (Runx2, Osterix, OCN, ALP) and lipogenic genes (FABP4, PPAR, CEBP, LPL) was detected by real-time quantitative polymerase chain reaction (real-time qPCR). The expression of p-Akt and Akt protein was detected by Western blot assay.

RESULTS

ALP staining and ARS staining showed that the overexpression of NT-3 could promote the differentiation into osteoblasts, while knockdown of NT-3 could inhibit that. Real-time qPCR showed that the overexpression of NT-3 could increase the expression of osteoblast genes, while knockdown of NT-3 could inhibit that. ORO staining showed that the overexpression of NT-3 could inhibit the differentiation into adipogenesis, while knockdown of NT-3 can promote that. Real-time qPCR showed that the overexpression of NT-3 could reduce the expression of lipogenic genes. while knockdown NT-3 could increase that. In addition, the overexpression of NT-3 increased p-Akt/Akt levels significantly, while knockdown NT-3 reduced that significantly.

CONCLUSION

NT-3 could promote the differentiation of mouse BMSCs into osteoblasts and inhibit their differentiation into adipogenesis.

摘要

目的

研究神经营养因子-3(NT-3)对骨髓间充质干细胞(BMSCs)成骨/成脂分化的影响。

方法

碱性磷酸酶(ALP)染色和茜素红染色(ARS)检测成骨分化。油红 O(ORO)染色检测成脂分化。实时定量聚合酶链反应(real-time qPCR)检测骨相关基因(Runx2、Osterix、OCN、ALP)和脂肪生成基因(FABP4、PPAR、CEBP、LPL)的表达。Western blot 检测 p-Akt 和 Akt 蛋白的表达。

结果

ALP 染色和 ARS 染色表明,NT-3 的过表达可以促进向成骨细胞分化,而 NT-3 的敲低则抑制了这种分化。实时 qPCR 显示,NT-3 的过表达可以增加成骨基因的表达,而 NT-3 的敲低则抑制了这种表达。ORO 染色表明,NT-3 的过表达可以抑制向脂肪生成分化,而 NT-3 的敲低可以促进这种分化。实时 qPCR 显示,NT-3 的过表达可以降低脂肪生成基因的表达,而敲低 NT-3 则可以增加这些基因的表达。此外,NT-3 的过表达显著增加了 p-Akt/Akt 水平,而敲低 NT-3 则显著降低了该水平。

结论

NT-3 可促进小鼠 BMSCs 向成骨细胞分化,抑制向脂肪生成分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccd2/7716693/f3c4e4356653/JMNI-20-591-g001.jpg

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