口腔医学 ›› 2022, Vol. 42 ›› Issue (9): 790-795.doi: 10.13591/j.cnki.kqyx.2022.09.005

• 基础研究 • 上一篇    下一篇

miR-155在炎症微环境下对牙周膜干细胞成骨分化的调控作用

刘煜清1, 龚瑶2, 赵苏峰1, 戴丽1   

  1. 1.南京大学医学院附属口腔医院儿童口腔科,江苏南京(210008);
    2.南京大学医学院附属口腔医院口腔颌面外科门诊,江苏 南京(210008)
  • 修回日期:2022-03-27 出版日期:2022-09-28 发布日期:2022-09-20
  • 通讯作者: 戴 丽 E-mail:16545505@qq.com
  • 基金资助:
    2021年度省中医药科技发展计划项目(MS2021041)

Regulation effect of miR-155 on osteogenic differentiation of periodontal ligament stem cells in inflammatory microenvironment

LIU Yuqing, GONG Yao, ZHAO Sufeng, DAI Li   

  1. Department of Pediatric Dentistry,Nanjing Stomatological Hospital Medical School of Nanjing University, Nanjing 210008, China
  • Revised:2022-03-27 Online:2022-09-28 Published:2022-09-20

摘要: 目的 研究miR-155在炎症微环境下对牙周膜干细胞(periodontal ligment stem cells,PDLSCs)成骨分化的调控作用。方法 将PDLSCs按照不同处理方法分为对照组、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)组、miR-阴性对照(NC)组、TNF-α+miR-NC组、TNF-α+miR-155抑制物组、miR-155组,采用荧光定量PCR检测miR-155、Runt相关转录因子2(recombinant runt related transcription factor 2,Runx2)、骨钙素(osteocalcin,OCN)、Ⅰ型胶原(collagenⅠ,Col-Ⅰ)、骨形态发生蛋白5(bone morphogenetic protein 5,BMP5)、骨形态发生蛋白10(bone morphogenetic protein 10,BMP10) mRNA表达水平;Western blot检测Runx2、OCN、Col-Ⅰ、BMP5、BMP10蛋白表达;茜素红染色检测细胞钙结节形成;双荧光素酶报告基因验证miR-155靶向BMP5、BMP10。结果 与对照组比较,TNF-α组PDLSCs中miR-155的表达水平明显升高,Runx2、OCN、Col-Ⅰ的mRNA和蛋白表达水平以及钙结节形成量降低(P<0.05);与miR-NC组比较,TNF-α+miR-NC组PDLSCs中Runx2、OCN、Col-Ⅰ的mRNA和蛋白表达水平及钙结节形成量降低,差异有统计学意义(P<0.05);与TNF-α+miR-NC组比较,TNF-α+miR-155抑制物组PDLSCs中Runx2、OCN、Col-Ⅰ的mRNA和蛋白表达水平及钙结节形成量明显升高(P<0.05);miR-155靶向负调控BMP5、BMP10表达。结论 炎症微环境下PDLSCs中miR-155表达增加,敲低miR-155可促进炎症微环境下PDLSCs成骨分化,靶向调控BMP5及BMP10是相关分子机制。

关键词: 牙周炎, miR-155, 牙周膜干细胞, 成骨分化, 骨形态发生蛋白5, 骨形态发生蛋白10

Abstract: Objective To study the regulatory effect of miR-155 on osteogenic differentiation of periodontal ligament stem cells (PDLSCs) in inflammatory microenvironment. Methods PDLSCs were cultured and divided into control group, tumor necrosis factor group-α(TNF-α) group, miR-negative control (NC) group, TNF-α+miR-NC group, TNF-α+miR-155 inhibitor group and miR-155 group according to different treatment methods. Fluorescence quantitative PCR was used to detect miR-155, recombinantrunt related transcription factor 2 (Runx2), osteocalcin (OCN), collagen Ⅰ (Col-Ⅰ),bone morphogenetic protein 5 (BMP5) and bone morphogenetic protein 10 (BMP10) expression levels; Western blot was used to detect Runx2, OCN, Col-Ⅰ, BMP5, BMP10 protein expression; alizarin red staining was used to detect the formation of calcium nodules in cells; the double luciferase reporter gene was used to verify that miR-155 targeted BMP5 and BMP10. Results Compared with the control group, the expression level of miR-155 in PDLSCs in the TNF-α group increased; the mRNA and protein expression levels of Runx2, OCN, Col-Ⅰ and the formation of calcium nodules decreased (P<0.05). Compared with the miR-NC group, the mRNA and protein expression levels of Runx2, OCN and Col-Ⅰ and the formation of calcium nodules in PDLSCs in the TNF-α+miR-NC group were decreased (P<0.05). Compared with the TNF-α+miR-NC group, the mRNA and protein expression levels of Runx2, OCN and Col-Ⅰ and the formation of calcium nodules in PDLSCs in the TNF-α+miR-155 inhibitor group increased (P<0.05). miR-155 negatively regulated the expressions of BMP5 and BMP10. Conclusion The expression of miR-155 in PDLSCs increases in inflammatory microenvironment. Knocking down miR-155 promotes the osteogenic differentiation of PDLSCs in inflammatory microenvironment. Targeting BMP5 and BMP10 is the relevant molecular mechanism.

Key words: periodontitis, miR-155, periodontal ligament stem cell, osteogenic differentiation, bone morphogenetic protein 5, bone morphogenetic protein 10

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