中国实用口腔科杂志

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炎性微环境中糖原合成酶激酶-3β对颌骨来源骨髓间充质干细胞成骨分化影响研究

胡祥翔a胡开进b,赵铱民a   

  1. 军事口腔医学国家重点实验室,第四军医大学口腔医学院 a修复科,b口腔外科,陕西  西安  710032
  • 出版日期:2017-01-15 发布日期:2017-03-28
  • 基金资助:

    国家重点研发计划子课题(2016YFC1102903)

  • Online:2017-01-15 Published:2017-03-28

摘要:

目的    探讨炎性微环境中糖原合成酶激酶-3β(GSK-3β)对颌骨来源间充质干细胞(JBMMSCs)成骨分化的影响。方法    应用慢病毒(shRNA)转染技术在JBMMSCs中敲减GSK-3β表达,利用白细胞介素(IL)-1β和肿瘤坏死因子(TNF)-α模拟炎症微环境。成骨诱导后利用Western Blot检测成骨相关蛋白表达,茜素红染色检测成骨效率。结果    敲减GSK-3β表达可增强JBMMSCs成骨诱导后的成骨相关蛋白表达,成骨效率增强。炎症微环境可显著下调正常JBMMSCs成骨诱导后的成骨相关蛋白表达,成骨效率明显降低,而对敲减GSK-3β表达的JBMMSCs成骨诱导后的成骨相关蛋白表达下调较弱,成骨效率降低较轻。结论    抑制GSK-3β既可促进JBMMSCs的成骨作用,又可减轻炎性微环境对JBMMSCs成骨的不良影响,为提高炎症状态下JBMMSCs促进组织再生提供了新的治疗靶点。

关键词: 糖原合成酶激酶-3&beta, 炎性微环境, 成骨诱导

Abstract:

Objective    To discuss the influence of glycogen synthase kinase-3β(GSK-3β)on osteogenesis of jaw bone marrow mesenchymal stem cells(JBMMSCs) in inflammatory microenvironment. Methods    Use shRNA to knock down the expression of GSK-3β in JBMMSCs. IL-1β and TNF-α were used to mimic inflammatory microenvironment. After osteogenesis,Western Blot was used to detect osteogenesis-related protein expression and Alizarin Staining was used to detect the efficiency of osteogenesis in different groups. Results    Expression of osteogenesis-related protein and efficiency of osteogenesis was highly up-regulated after knocking-down of GSK-3β in JBMMSCs. Inflammatory microenvironment could significantly down-regulate the expression of osteogenesis-related protein and efficiency of osteogenesis in ordinary JBMMSCs,while knocking-down GSK-3β could attenuate this effect. Conclusion    Knocking-down of GSK-3β in JBMMSCs can both increase the efficiency of osteogenesis and resist the adverse effect of inflammatory microenvironment on osteogenesis,thus GSK-3β is a potential target for improving the regeneration in inflammatory microenvironment.

Key words: glycogen synthase kinase-3&beta, ;inflammatory microenvironment;osteogenesis