上海口腔医学 ›› 2018, Vol. 27 ›› Issue (1): 28-33.doi: 10.19439/j.sjos.2018.01.007

• 论著 • 上一篇    下一篇

周期性牵张应力作用下KLF5对人牙周膜细胞增殖和成骨分化的影响

高锦瑜1, 余小琴2, 王军强3   

  1. 1.延安大学附属医院 口腔正畸科,陕西 延安 716000
    2.安康市人民医院 口腔科,陕西 安康 725000
    3.延安大学附属医院 口腔修复科,陕西 延安 716000
  • 收稿日期:2017-06-27 修回日期:2017-09-04 出版日期:2018-02-25 发布日期:2018-03-05
  • 通讯作者: 余小琴, E-mail: xiaoqinakkq@qq.com
  • 作者简介:高锦瑜(1969-),女,学士,副主任医师,E-mail: inyujyya@163.com

KLF5 modulates proliferation and osteogenic differentiation of human periodontal ligament cells subjected to cyclic tensile stress

GAO Jin-yu1, YU Xiao-qing2, WANG Jun-qiang3   

  1. 1.Department of Orthodontics, Affiliated Hospital of Yan'an University. Yan'an 716000
    2.Department of Stomatology, People's Hospital of Ankang City. Ankang 725000
    3.Department of Prosthodontics, Affiliated Hospital of Yan'an University. Yan'an 716000, Shaanxi Province, China
  • Received:2017-06-27 Revised:2017-09-04 Online:2018-02-25 Published:2018-03-05

摘要: 目的: 探讨周期性牵张应力(cyclic tensile stress, CTS) 作用下Kruppel样转录因子5 (Kruppel-like factor 5, KLF5) 在人牙周膜细胞 (human periodontal ligament cells, hPDLCs) 中的表达及其对 hPDLCs增殖和成骨分化的影响。方法: 酶解组织块法体外培养hPDLCs,对其施加形变率10%,频率0.5 Hz的周期性牵张应力1、4、8、12、24 h,采用RT-PCR 和Western印迹法检测细胞中KLF5 mRNA和蛋白的表达。转染siRNA(si-KLF5)至hPDLCs沉默KLF5表达,RT-PCR检测KLF5 mRNA的表达。同时,将过表达碱性成纤维细胞生长因子(basic fibroblast growth factor,bFGF、FGF2)的pcDNA3.1-FGF2转染至稳定转染si-KLF5的hPDLCs,加力8 h 后,以CCK8法检测各组细胞的增殖活性,碱性磷酸酶(alkaline phosphatase, ALP)试剂盒检测ALP活性,RT-PCR检测成骨分化因子Runx2和Osterix的mRNA表达,Western印迹法检测Runx2、Osterix、FGF2、GSK-3β、P-GSK-3β (ser 9)、β-catenin蛋白的表达。采用SPSS22.0 软件包对数据进行统计学分析。结果: 10% CTS刺激呈时间依赖性地诱导hPDLCs中KLF5 mRNA 和蛋白表达。si-KLF5转染可显著抑制10% CTS诱导的hPDLCs的增殖,降低其ALP活性,减少Runx2和Osterix的mRNA和蛋白表达,并抑制FGF2-GSK-3β/β-catenin信号通路的激活;而过表达FGF2可以部分逆转沉默KLF5对hPDLCs增殖和成骨分化的抑制效应。结论: 周期性牵张应力作用下,KLF5通过FGF2-GSK-3β/ /β-catenin信号通路影响人牙周膜细胞的增殖和成骨分化。

关键词: KLF5, 人牙周膜细胞, 细胞增殖, 成骨分化

Abstract: PURPOSE: To investigate the expression of Kruppel-like factor 5 (KLF5) in human periodontal ligament cells (hPDLCs) under cyclic tensile stress (CTS) and its effect on proliferation and osteogenic differentiation of hPDLCs. METHODS: hPDLCs were primarily cultured in vitro by tissue explant and enzyme digestion method. RT-PCR and Western blot were used to detect mRNA and protein expression of KLF5 in hPDLCs stimulated by 10% CTS at a frequency of 0.5 Hz for 1, 4, 8, 12 and 24 h, respectively.KLF5 was then knocked-down in hPDLCs using siRNA (si-KLF5) and its mRNA expression was determined by RT-PCR. Meanwhile, basic fibroblast growth factor (FGF2) was overexpressed in KLF-5 silenced hPDLCs by using pcDNA3.1-FGF2. After stimulation with CTS for 8 h, the proliferation of hPDLCs was assayed by CCK-8 kit, alkaline phosphatase (ALP) activity was assayed by ALP kit, the mRNA expression of Runx2 and Osterix was examined by RT-PCR, and the protein expression of Runx2, Osterix, FGF2, GSK-3β, P-GSK-3β (ser 9), β-catenin was determined by Western blot. The data were analyzed using SPSS 22.0 software package. RESULTS: Stimulation with 10% CTS time-dependently induced mRNA and protein expression of KLF5 in hPDLCs. Transfection of si-KLF5 significantly reduced the proliferation of hPDLCs, decreased ALP activity and expression of Runx2 and Osterix in hPDLCs stimulated by 10% CTS. Simultaneously, CTS-induced activation of FGF2-GSK-3β/β-catenin signaling pathway was also inhibited by si-KLF5 transfection. However, overexpression of FGF2 can partly neutralized the inhibitiory effect of si-KLF5 on proliferation and osteogenic differentiation of hPDLCs subjected to 10% CTS. CONCLUSIONS: KLF5 promotes proliferation and osteogenesis differentiation of hPDLCs subjected to cyclic tensile stress through FGF2-GSK-3β/β-catenin signaling pathway.

Key words: KLF5, Human periodontal ligament cells, Cell proliferation, Osteogenic differentiation

中图分类号: