[GLIS家族锌指蛋白2 (GLIS2)负调控Wnt/β-catenin通路抑制人骨髓间充质干细胞成骨分化]。

Yanli Zhao, Zhiqiang Kang, Yu Mao, Fang Luo, Yajie Huo
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引用次数: 0

摘要

目的探讨GLIS家族锌指蛋白2 (GLIS2)调控Wnt/β-catenin通路及其对人骨髓间充质干细胞(BMMSCs)分化的影响。方法将人骨髓间充质干细胞随机分为空白组、成骨诱导组、GLIS2基因过表达组(ad-GLIS2)、ad-GLIS2阴性对照组、基因敲低组(si-GLIS2)和si-GLIS2阴性对照组(si-NC)。通过逆转录- pcr检测各组GLIS2 mRNA的表达,判断转染状态;采用PNPP法检测碱性磷酸酶(ALP)活性,茜素红染色法检测钙化结节形成情况,测定其成骨性能;采用T细胞因子/淋巴细胞增强因子(TCF/LEF)报告试剂盒检测细胞内Wnt/β-catenin通路的激活情况;Western blot法检测GLIS2、runt相关转录因子2 (Runx2)、骨桥蛋白(OPN)、osterix的表达。gst -pull - down验证了GLIS2与β-catenin的相互作用。结果与空白组比较,成骨诱导组BMMSCs ALP活性和钙化结节形成增加,Wnt/β-catenin通路活性和成骨分化相关蛋白表达增加,成骨能力增强,GLIS2表达降低。上调GLIS2的表达可抑制BMMSCs的成骨分化,而抑制Wnt/β-catenin通路的活性,抑制成骨分化相关蛋白的表达。下调GLIS2的表达可促进BMMSCs的成骨分化,提高Wnt/β-catenin通路活性和成骨分化相关蛋白的表达。β-catenin与GLIS2存在相互作用。结论GLIS2可能负调控Wnt/β-catenin通路的激活,影响骨髓间充质干细胞成骨分化。
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[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].

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.

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