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[GLIS家族锌指蛋白2(GLIS2)负向调节Wnt/β-连环蛋白通路以抑制人骨髓间充质干细胞的成骨分化]

[GLIS family zinc finger protein 2 (GLIS2) negatively regulates the Wnt/β-catenin pathway to inhibit the osteogenic differentiation of human bone marrow mesenchymal stem cells].

作者信息

Zhao Yanli, Kang Zhiqiang, Mao Yu, Luo Fang, Huo Yajie

机构信息

Department of Endocrine, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, China.

Department of Endocrine, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, China. *Corresponding author, E-mail:

出版信息

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2023 Feb;39(2):159-164.

Abstract

Objective To investigate how the human GLIS family zinc finger protein 2 (GLIS2) regulate the Wnt/β-catenin pathway and its influence on the differentiation of human bone marrow mesenchymal stem cells (BMMSCs). Methods Human BMMSCs were randomly divided into blank group, osteogenic induction group, GLIS2 gene overexpression (ad-GLIS2) group, ad-GLIS2 negative control group, gene knockdown (si-GLIS2) group, and si-GLIS2 negative control (si-NC) group. The expression of GLIS2 mRNA in each group was detected by reverse transcription-PCR to determine the transfection status; alkaline phosphatase (ALP) activity was detected by phenyl-p-nitrophenyl phosphate (PNPP), and calcified nodule formation was tested by alizarin red staining to determine its osteogenic properties; the activation of intracellular Wnt/β-catenin pathway was detected by T cell factor/lymphoid enhancer factor (TCF/LEF) reporter kit; the expression of GLIS2, Runt-related transcription factor 2 (Runx2), osteopontin (OPN), and osterix was detected by Western blot analysis. The interaction between GLIS2 and β-catenin was verified by GST-pulldown. Results Compared with the blank group, the ALP activity and calcified nodule formation of BMMSCs in the osteogenic induction group increased, and the Wnt/β-catenin pathway activity and the expression of osteogenic differentiation-related proteins increased, the osteogenic ability increased, while the expression of GLIS2 decreased. Up-regulating the expression of GLIS2 could inhibit the osteogenic differentiation of BMMSCs, while suppress the activity of the Wnt/β-catenin pathway and the expression of osteogenic differentiation-related proteins on the contrary. Down-regulating the expression of GLIS2 could promote the osteogenic differentiation of BMMSCs, and improve the activity of the Wnt/β-catenin pathway and the expression of osteogenic differentiation-related proteins. There was an interaction between β-catenin and GLIS2. Conclusion GLIS2 may negatively regulate the activation of Wnt/β-catenin pathway and affect the osteogenic differentiation of BMMSCs.

摘要

目的 探讨人GLIS家族锌指蛋白2(GLIS2)如何调控Wnt/β-连环蛋白信号通路及其对人骨髓间充质干细胞(BMMSCs)分化的影响。方法 将人BMMSCs随机分为空白组、成骨诱导组、GLIS2基因过表达(ad-GLIS2)组、ad-GLIS2阴性对照组、基因敲低(si-GLIS2)组和si-GLIS2阴性对照(si-NC)组。采用逆转录-聚合酶链反应检测各组GLIS2 mRNA表达以确定转染情况;用对硝基苯磷酸酯(PNPP)检测碱性磷酸酶(ALP)活性,用茜素红染色检测钙化结节形成以确定其成骨特性;用T细胞因子/淋巴细胞增强因子(TCF/LEF)报告基因试剂盒检测细胞内Wnt/β-连环蛋白信号通路的激活情况;采用蛋白质免疫印迹法检测GLIS2、 runt相关转录因子2(Runx2)、骨桥蛋白(OPN)和osterix的表达。通过谷胱甘肽S-转移酶沉降实验(GST-pulldown)验证GLIS2与β-连环蛋白之间的相互作用。结果 与空白组比较,成骨诱导组BMMSCs的ALP活性和钙化结节形成增加,Wnt/β-连环蛋白信号通路活性及成骨分化相关蛋白表达增加,成骨能力增强,而GLIS2表达降低。上调GLIS2表达可抑制BMMSCs的成骨分化,同时抑制Wnt/β-连环蛋白信号通路活性及成骨分化相关蛋白的表达;下调GLIS2表达可促进BMMSCs的成骨分化,提高Wnt/β-连环蛋白信号通路活性及成骨分化相关蛋白的表达。β-连环蛋白与GLIS2之间存在相互作用。结论 GLIS2可能负向调控Wnt/β-连环蛋白信号通路的激活并影响BMMSCs的成骨分化。

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