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白细胞介素1β对人牙周膜干细胞和骨髓间充质干细胞骨向分化的影响 被引量:2

The effect of interleukin-1βon the osteogenic differentiation of periodontal ligament stem cells and bone marrow mesenchymal stem cells
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摘要 目的研究白细胞介素1β(IL-1β)作用下人牙周膜干细胞(PDLSC)和骨髓间充质干细胞(BMSC)骨向分化的差异。方法应用茜素红染色、碱性磷酸酶(ALP)活性检测、细胞增殖能力(MTT)法和实时荧光聚合酶链反应(PCR)对PDLSC和BMSC在IL-1β作用下的骨向分化能力进行检测,并比较两者之间的差异。实验组为含有IL-1β的各处理组,对照组内未加IL-1β。采用单因素方差分析和t检验对数据进行统计分析。结果随IL-1β浓度的增高,PDLSC形成矿化结节减少,茜素红染色逐渐变浅;而BMSC骨向分化能力未见明显减弱;ALP活性实验结果表明,在7 d时PDLSC各实验组与对照组相比差异具有统计学意义(F=2361.11,P<0.001),BMSC各实验组与对照组相比ALP活性差异具有统计学意义(F=240.68,P<0.001);在14 d时PDLSC随炎症因子浓度增高,ALP活性显著降低,差异具有统计学意义(F=1519.89,P<0.001),BMSC在IL-1β浓度为0.001、0.01、1 ng/mL的实验组与对照组相比ALP活性差异具有统计学意义(F=22.52,P<0.001),两种干细胞在IL-1β最大浓度时(1 ng/mL)ALP活性最低;MTT结果表明,IL-1β能抑制干细胞的增殖能力,与PDLSC相比,BMSC增殖能力较低。实时荧光PCR结果显示,与对照组相比,两种干细胞实验组内ALP、Col-1、OCN和Runx2 m RNA表达水平均降低,BMSC内实验组中骨向分化基因表达与PDLSC内实验组相比,差异均有统计学意义(P<0.05)。结论在IL-1β作用下,BMSC的成骨能力较PDLSC高。 Objective To investigate the effect of interleukin-1β(IL-1β)on the osteogenic differentiation of periodontal ligament stem cells(PDLSCs)and bone marrow mesenchymal stem cells(BMSCs).Methods The osteogenic differentiation ability of PDLSCs and BMSCs was tested by Alizarin Red staining,alkaline phosphatase(ALP)activity,MTT,and real-time PCR with the presence of IL-1β.The PDLSCs or BMSCs cultured with IL-1βwere the experimental groups,while the control group was cultured without IL-1β.One-Way ANOVA and t-test were applied to perform the statistical analysis of the data.Results Mineralization staining showed that an inhibitory effect of IL-1βon the osteogenic differentiation of PDLSCs with increasing dose.However,BMSCs were more resistant to the inflammatory cytokine compared to PDLSCs in terms of a stronger alizarin red staining.The results of ALP activity test showed that a significant difference between the PDLSCs experimental groups and the control group was found at 7 days(F=2361.11,P<0.001);for BMSCs,a similar result was also observed between the experimental groups and the control group(F=240.68,P<0.001).At 14 days,with the increase of inflammatory factor concentration,the activity of ALP in PDLSCs decreased significantly(F=1519.89,P<0.001).The ALP activity of the experimental groups with IL-1βconcentration of 0.001,0.01 and 1 ng/mL in BMSCs was significantly different from that of the control group(F=22.52,P<0.001).ALP activity of the two kinds of stem cells was the lowest with the presence of the maximum concentration of IL-1β(1 ng/mL).Proliferation results showed that IL-1βexhibited inhibitory effects on cell proliferation and BMSCs possessed a lower proliferative potential than PDLSCs.Real-time PCR analysis of osteoblast lineage gene expression revealed that the IL-1βsuppressed the expression levels of ALP,Col-1,OCN and Runx2 mRNA in PDLSCs and BMSCs at 14 days compared with the control group.The difference of mRNA expression levels was statistically significant between the BMSCs experimental group and the PDLSCs experimental group.Conclusions A significant difference on the osteogenesis between PDLSCs and BMSCs was observed.Compared with PDLSCs,BMSCs showed a stronger capacity of modulation in local microenvironment via anti-inflammatory functions.
作者 张静 李晨晨 孟箭 Zhang Jing;Li Chenchen;Meng Jian(Xuzhou Institute of Medical Science,Xuzhou 221009,China;Xuzhou Clinical College of Xuzhou Medical University,Xuzhou 221009,China;Department of Stomatology,Xuzhou Central Hospital,Xuzhou 221009,China)
出处 《中华口腔医学研究杂志(电子版)》 CAS 2020年第2期88-94,共7页 Chinese Journal of Stomatological Research(Electronic Edition)
基金 国家自然科学基金(31700814) 徐州市科技项目(KC18032)。
关键词 炎症 细胞因子类 干细胞 细胞分化 骨向分化 Inflammation cytokines Stem cells Cell differentiation Osteogenic differentiation
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  • 1Pihlstrom BL, Michalowicz BS, Johnson NW. Periodontal disease[J]. Lancet, 2005, 366(9499) : 1809-1820.
  • 2Park JY, Jeon SH, Choung PH. Efficacy of periodontal stem cell transplantation in the treatment of advanced periodontitis [J]. Cell Transplant, 2011, 20(2): 271-285.
  • 3Seo BM, Miura M, Gronthos S, et al. Investigation of multipotent postnatal stem ceils from human periodontal ligament [J]. Lancet, 2004, 364(9429) : 149-155.
  • 4Mrozik K, Gronthos S, Shi S, et al. A method to isolate, purify, and characterize human periodontal ligament stem cells [J]. Methods Mol Biol, 2010, 666 : 269-284.
  • 5Liu Y, Zheng Y, Ding G, et al. Periodontal ligament stem cell-mediated treatment for periodontitis inminiature swine [J]. Stem Cells, 2008, 26 : 1065-1073.
  • 6Zhang S, Barros SP, Moretti AJ, et al. Epigenetic regulation of TNFA expression in periodontal disease [J]. J Periodontol, 2013, 84(11):1606-16.
  • 7Takahashi K, Takashiba S, Nagai A, et al. Assesement of interleukin-6 in the pathogenesis of periodontal disease [J]. J Periodontol, 1994, 65(2): 147-153.
  • 8Li Q, Verma IM. NF-kappaB regulation in the immune system[J]. Nat. Rev. Immunol, 2002, 2 (10): 725-734.
  • 9Jotwani R, Moonga BS, Gupta S, et al. Nuclear factor- kappa p50 subunits in chronic periodontitis and porphy- romonas gingivalis lipopolysaccharide-pulsed dendritic cells [J]. Ann N Y Acad Sci, 2010, 1192: 278-285.
  • 10Shahnazari M, Yao W, Corr M, et al. Targeting the Wnt signaling pathway to augment bone formation [J]. Curr Osteoporos Rep, 2008, 6(4):142-148.

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