Mechanism of Astragaloside IV in Promoting Osteogenic Differentiation

PTEN公司 张力素 PI3K/AKT/mTOR通路 蛋白激酶B 碱性磷酸酶 化学 磷酸酶 免疫印迹 细胞分化 细胞生物学 信号转导 分子生物学 磷酸化 生物 生物化学 基因
作者
Yao Zhu,Cheng‐Yu Lin,Xudong Zhang,Zuyun Qiu,Lei Shi,Jianmin Li
出处
期刊:Current Molecular Medicine [Bentham Science Publishers]
卷期号:25
标识
DOI:10.2174/0115665240333454241203050356
摘要

This study focuses on exploring the impact of Astragaloside IV [AS-IV] on osteogenic differentiation. Osteogenic differentiation was induced in rat osteoblasts, following which treatment with AS-IV at varied doses was performed. Using Alizarin red staining and alkaline phosphatase [ALP] detection assay, the osteogenic differentiation of the cells was investigated. The expressions of osteogenic differentiation-related genes were determined by quantitative real-time polymerase chain reaction [qRT-PCR]. The phosphatidylinositol 3-kinase [PI3K]/protein kinase B [Akt] signaling pathwayassociated protein expressions were examined using Western blot. After osteoblasts were transfected with protein tyrosine phosphatase non-receptor type 2 [PTPN2] overexpression plasmid, the impact of PTPN2 on osteoblasts treated with AS-IV was examined. AS-IV treatment enhanced osteogenic differentiation and up-regulated the expression of osteogenic differentiation-related genes, as well as the levels of p- PI3K/PI3K and p-AKT/AKT, while reducing PTEN protein production in osteoblasts. Overexpression of phosphatase and tensin homolog [PTEN] inhibited osteogenic differentiation, and PTPN2 overexpression counteracted the effects of AS-IV on osteogenic differentiation. AS-IV contributing to osteogenic differentiation may be related to the PTPN2-mediated PTEN/PI3K/Akt pathway.

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