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.
J Musculoskelet Neuronal Interact. 2020 Dec 1;20(4):591-599.
To investigate the effect of neurotrophin-3 (NT-3) on osteogenic/adipogenic differentiation of bone marrow mesenchymal stem cells (BMSCs).
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.
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.
NT-3 could promote the differentiation of mouse BMSCs into osteoblasts and inhibit their differentiation into adipogenesis.
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。
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。
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。
NT-3 可促进小鼠 BMSCs 向成骨细胞分化,抑制向脂肪生成分化。