›› 2020, Vol. 11 ›› Issue (2): 120-124.doi: 10.3969/j.issn.1674-8603.2020.02.012

• 论著 • 上一篇    下一篇

炎性环境下FSTL1对小鼠骨髓间充质干细胞成骨性能的影响

金齐尧1,毛广艳2,邓威3,王晨星4,李怀奇1,王东苗5,叶金海2   

  1. 1. 南京医科大学附属口腔医院
    2. 南京医科大学附属口腔医院颌面外科
    3. 南京医科大学附属口腔医院口腔颌面外科
    4. 1.南京医科大学口腔疾病研究江苏省重点实验室 2.南京医科大学附属口腔医院口腔颌面外科
    5. 南京医科大学口腔医学研究所,南京医科大学口腔医学院口腔颌面外科
  • 收稿日期:2020-04-13 修回日期:2020-05-30 出版日期:2020-06-25 发布日期:2020-07-08
  • 通讯作者: 金齐尧 E-mail:jqy1007@163.com
  • 基金资助:
    国家自然科学基金;江苏省医学重点人才;江苏高校优势学科建设工程项目

Effect of FSTL1 on osteogenesis of mouse bone marrow mesenchymal cells in inflammatory environment

  • Received:2020-04-13 Revised:2020-05-30 Online:2020-06-25 Published:2020-07-08
  • Contact: Qi-Yao JIN E-mail:jqy1007@163.com

摘要: 目的:研究炎性环境下卵泡抑素样蛋白1(FSTL1)对小鼠骨髓间充质干细胞(mBMSCs)成骨性能的影响。方法:将mBMSCs转染慢病毒,改变细胞FSTL1的表达,通过CCK-8法检测细胞增殖活性。转染慢病毒的mBMSCs经过10 ng/mL的肿瘤坏死因子α(TNF-α)刺激后,再予以成骨诱导;通过碱性磷酸酶(ALP)和茜素红染色实验,观察mBMSCs的成骨能力的变化;通过实时定量PCR检测细胞Ⅰ型胶原蛋白(Col1)、骨桥蛋白(Opn)、骨钙素(Ocn)等成骨相关基因的表达。结果:通过慢病毒转染能够有效地改变mBMSCs内Fstl1基因的表达,并且不影响细胞增殖活性(P>0.05)。在含有10?ng/mL TNF-α的炎症环境中,与对照组相比,过表达FSTL1的mBMSCs成骨诱导后ALP和茜素红染色变浅,成骨相关基因表达降低(P<0.05);而敲减FSTL1的mBMSCs成骨诱导后ALP和茜素红染色变深,成骨相关基因表达升高(P<0.05)。结论:FSTL1促进了炎症对mBMSCs成骨性能的抑制作用,抑制FSTL1能有效地减轻炎症对BMSCs的影响

关键词: 卵泡抑素样蛋白1, 骨髓间充质干细胞, 成骨分化, 炎症

Abstract: Objective:To investigate whether follistatin-like protein 1 (FSTL1) can affect the osteogenic performance of mouse bone marrow mesenchymal stem cells (mBMSCs) in an inflammatory environment.?Methods:?mBMSCs were transfected with lentivirus to change the expression of FSTL1, and the proliferation activity of these cells was detected by CCK-8experiment. The mBMSCs transfected with lentivirus were stimulated with 10?ng/mL TNF-α, and then induced into osteoblasts.?Alkaline phosphatase (ALP) and alizarin red staining experiments were used to detect the changes of osteogenic ability of mBMSCs; ?the expression of collagen type Ⅰ collagen (Col1), osteopontin (Opn), osteocalcin (Ocn) was detected by real-time quantitative PCR.?Results:?Lentivirus transfection could effectively change the expression of FSTL1 gene in mBMSCs, and there was no significant difference in the proliferation activity of these cells (P>0.05). In the inflammatory environment containing 10?ng/mL TNF-α, compared with the control group, mBMSCs overexpressing FSTL1 had lighter ALP and alizarin red staining results after osteogenic induction, and the expression of Col1, Opn, and Opn genes decreased (P<0.05);mBMSCs knockeddown FSTL1 had darker ALP and alizarin red staining results after osteogenic induction, and the expression of Col1, Opn, and Opn genes increased (P<0.05). ?Conclusions:?FSTL1 promotes the inhibitory effect of inflammation on the osteogenic performance of mBMSCs, and inhibiting FSTL1 can effectively reduce the effect of inflammation on BMSCs.

Key words: follistatin-like protein 1, bone marrow mesenchymal stem cells, Inflammation