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牛膝甾酮在促进大鼠骨髓间充质干细胞成骨分化中的作用

孙祥燚 李敏 龙如超 杨志华 陈强 冯纯智

临床骨科杂志2025,Vol.28Issue(3):444-448,5.
临床骨科杂志2025,Vol.28Issue(3):444-448,5.DOI:10.3969/j.issn.1008-0287.2025.03.047

牛膝甾酮在促进大鼠骨髓间充质干细胞成骨分化中的作用

Role of inokosterone in promoting osteogenic differentiation of bone marrow mesenchymal stem cells

孙祥燚 1李敏 2龙如超 1杨志华 1陈强 1冯纯智1

作者信息

  • 1. 杭州师范大学附属萧山医院(浙江萧山医院)骨科,浙江 杭州 311200
  • 2. 杭州萧山区义桥卫生服务中心,浙江 杭州 311200
  • 折叠

摘要

Abstract

Objective To investigate the role of inokosteroneon in promoting the osteogenic differentiation of bone marrow mesenchymal stem cells(BMSCs).Methods BMSCs were managed with varying doses of inokosterone.Os-teogenic differentiation was assessed by alizarin red staining,while cell proliferation activity was measured using CCK-8 assay.Cytokine expression levels were determined by ELISA,and protein expression was analyzed via Western blot.The effects of BMP2 siRNA interference and overexpression on cell proliferation were evaluated through CCK-8 assay and Western blot analysis.Results Alizarin red staining demonstrated that inokosterone significantly enhanced osteogenic differentiation of BMSCs,with particularly pronounced effects at the high dose(200 mg/L).Compared with the blank control group,all tested doses of inokosterone increased BMSC proliferation activity(P<0.05),and promoted the expression of osteogenic markers including Collagen I,ALP,OC and related differentiation proteins(P<0.05).BMP2 siRNA+inokosterone group showed significantly higher proliferation activity than the BMP2 siR-NA-only group(P<0.01).Conclusions Inokosterone promotes proliferation and osteogenic differentiation of rat BMSCs,potentially through modulation of the BMP2/Smad signaling pathway by targeting BMP2.

关键词

牛膝甾酮/骨髓间充质干细胞/成骨分化/骨形态发生蛋白

Key words

achyranosterone/bone marrow mesenchymal stem cells/osteogenic differentiation/bone morphogenetic proteins

分类

医药卫生

引用本文复制引用

孙祥燚,李敏,龙如超,杨志华,陈强,冯纯智..牛膝甾酮在促进大鼠骨髓间充质干细胞成骨分化中的作用[J].临床骨科杂志,2025,28(3):444-448,5.

基金项目

浙江省杭州市科技局科技计划项目(编号:20201231Y120) (编号:20201231Y120)

临床骨科杂志

1008-0287

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