实用医学杂志 ›› 2022, Vol. 38 ›› Issue (22): 2774-2779.doi: doi:10.3969/j.issn.1006⁃5725.2022.22.003

• 基础研究 • 上一篇    下一篇

锁阳多糖通过激活PI3K/Akt/GSK3β/β-catenin信号通路促进MC3T3-E1细胞成骨分化

胡俊1 谈荣珍1 袁忠1 杨盼盼1 张楚焌1 张斌1 沈云峰2    

  1. 1 南昌市洪都中医院骨伤七科(南昌 330008);2 南昌大学第二附属医院内分泌代谢科(南昌 330006)

  • 出版日期:2022-11-25 发布日期:2022-11-25
  • 通讯作者: 沈云峰 E⁃mail:594946095@qq.com
  • 基金资助:
    江西省重点研发计划(编号:20192BBG70027)

Cynomorium songaricum polysaccharide promotes osteogenic differentiation of MC3T3⁃E1 cells by activat⁃ ing PI3K/Akt/GSK3β/β⁃catenin signaling pathway

HU Jun*,TAN Rongzhen,YUAN Zhong,YANG Panpan, ZHANG Chujun,ZHANG Bin,SHEN Yunfeng.   

  1. Seventh Department of Orthopaedics,Nanchang Hongdu Hospital of TCM,Nanchang 330008,China

  • Online:2022-11-25 Published:2022-11-25
  • Contact: SHEN Yunfeng E⁃mail:594946095@qq.com

摘要:

目的 MC3T3⁃E1 小鼠前成骨细胞中 PI3K/Akt/GSK3β/β⁃catenin 信号通路的角度,揭示锁 阳多糖(cynomorium songaricum polysaccharide,CSP)的促成骨分化机制。方法 使用含有不同浓度 CSP 成骨诱导液培养 MC3T3⁃E1 细胞,在第 1、3、5、7 天采用 MTT 法检测细胞活力。随后分为 Con 组(0 μg/mL CSP)、CSP 组(100 μg/mL CSP)及 CSP +BEZ 组(100 μg/mL CSP 50 μmol/L BEZ(PI3K 特异性抑制剂)); 干预 14 d 后采用茜素红染色观察比较 MC3T3⁃E1 的成骨分化情况、Real⁃time PCR 定量分析相关成骨分 mRNA,如 Runt 相关转录因子 2(Runx2)、β⁃连环蛋白(β⁃catenin)、骨钙素(Osteocalcin)、Ⅰ型胶原蛋白 CollagenⅠ)的表达水平;并使用 Western blot 法检测 Runx2、CollagenⅠ、Osteocalcin 成骨相关蛋白;PI3K/ Akt/GSK3β/β⁃catenin 通路蛋白的表达情况,以及免疫荧光检测 β⁃catenin 的核易位情况。结果 Con 0 μg/mL)相比,CSP 干预均可有效促进 MC3T3⁃E1 增殖,100 μg/mL 的效果更加明显。与 Con 组比较,CSP 可有效促进 MC3T3⁃E1 细胞茜素红染色的阳性率,以及成骨相关的 mRNA、蛋白表达水平(P < 0.05),以及 PI3K、p⁃PI3K、Akt、p⁃Akt、GSK3β、p⁃GSK3β、β⁃catenin 蛋白表达(P < 0.05),同时还可促进 β⁃catenin 入核; 但是这些促进作用均可被 BEZ 逆转。结论 CSP 可能通过激活 PI3K/AKT/GSK3β/β⁃catenin 通路,诱导 MC3T3⁃E1细胞成骨分化。

关键词:

Abstract:

Objective To study the effect of Cynomorium songaricum polysaccharide(CSP)on the osteo⁃ genic differentiation of MC3T3 ⁃ E1 mouse osteoblast cell line through PI3K/Akt/GSK3β/β ⁃ catenin pathway. Methods MC3T3⁃E1 was cultured in osteogenic induction fluid with different concentrations of CSP. The cell viability was detected by MTT method on the 1st,3rd,5th,and 7th day. And then the cells were divided into Con group(0 μg/mL CSP),CSP group(100 μg/mL CSP)and CSP + BEZ group(100 μg/mL CSP and 50 μmol/L BEZ (PI3K specific inhibitor)). After 14 days of intervention,the cells in each group were stained with Alizarin Red to observe the osteogenic differentiation. Real⁃time quantitative PCR was utilized to analyze quantitatively the mRNA levels of osteogenic differentiation⁃related markers ,including Runt⁃related transcription factor 2 (Runx2), β⁃catenin,osteocalcin,collagen I;and western blotting was used to detect the protein expression of osteogenic differentiation⁃related proteins ,including Runx2 ,collagen I ,osteocalcin ,and proteins of PI3K/Akt/GSK3 β / β ⁃catenin pathway. And the immunofluorescence was applied to detect the nuclear translocation of β ⁃catenin. Results Compared with that in the Con group,the proliferation of MC3T3⁃E1 was effectively promoted in the CSP group and CSP + BEZ group,and the effect of 100 μg/mL CSP was more significant. CSP(100 μg/mL)could effectively promote the positive rate of Alizarin Red staining in MC3T3⁃E1 cells,as well as the expression levels of osteogenic differentiation⁃related proteins and mRNA(P < 0.05),and PI3K,p⁃PI3K,Akt,P⁃Akt,GSK3β,p⁃ GSK3β,and β⁃catenin protein expression(P < 0.05). CSP can also promote β⁃catenin into the nucleus;but this promotion effects can be reversed by BEZ. Conclusion CSP may induce osteogenic differentiation of MC3T3⁃E1cells by activating the PI3K/AKT/GSK3β/β⁃catenin pathway.

Key words:

osteoporosis Cynomorium songaricum polysaccharide PI3K/AKT/GSK3β/β ? catenin pathway osteogenic differentiation ,