Yildirim Selin, Zibandeh Noushin, Genc Deniz, Ozcan Elif Merve, Goker Kamil, Akkoc Tunc
Division of Pediatric Allergy-Immunology, Faculty of Medicine, Marmara University, 34890 Istanbul, Turkey.
Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Marmara University, 34890 Istanbul, Turkey.
Stem Cells Int. 2016;2016:4682875. doi: 10.1155/2016/4682875. Epub 2015 Dec 6.
Aim. To compare the effects of various mesenchymal stem cells, those isolated from human exfoliated deciduous teeth (SHEDs), dental pulp stem cells (DPSCs), and dental follicle stem cells (DFSCs), on human peripheral blood mononuclear cells (PBMCs). Method. Mesenchymal stem cells were isolated from three sources in the orofacial region. Characterization and PCR analyses were performed. Lymphocytes were isolated from healthy peripheral venous blood. Lymphocytes were cocultured with stem cells in the presence and absence of IFN-γ and stimulated with anti-CD2, anti-CD3, and anti-CD28 for 3 days. Then, lymphocyte proliferation, the number of CD4(+)FoxP3(+) T regulatory cells, and the levels of Fas/Fas ligand, IL-4, IL-10, and IFN-γ in the culture supernatant were measured. Results. The DFSCs exhibited an enhanced differentiation capacity and an increased number of CD4(+)FoxP3(+) T lymphocytes and suppressed the proliferation and apoptosis of PBMCs compared with SHEDs and DPSCs. The addition of IFN-γ augmented the proliferation of DFSCs. Furthermore, the DFSCs suppressed IL-4 and IFN-γ cytokine levels and enhanced IL-10 levels compared with the other cell sources. Conclusion. These results suggest that IFN-γ stimulates DFSCs by inducing an immunomodulatory effect on the PBMCs of healthy donors while suppressing apoptosis and proliferation and increasing the number of CD4(+)FoxP3(+) cells.
目的。比较从人脱落乳牙(SHEDs)、牙髓干细胞(DPSCs)和牙囊干细胞(DFSCs)中分离出的各种间充质干细胞对人外周血单个核细胞(PBMCs)的影响。方法。从口腔面部区域的三个来源分离间充质干细胞。进行了表征和PCR分析。从健康的外周静脉血中分离淋巴细胞。淋巴细胞在有和没有IFN-γ的情况下与干细胞共培养,并用抗CD2、抗CD3和抗CD28刺激3天。然后,测量淋巴细胞增殖、CD4(+)FoxP3(+)调节性T细胞数量以及培养上清液中Fas/Fas配体、IL-4、IL-10和IFN-γ的水平。结果。与SHEDs和DPSCs相比,DFSCs表现出增强的分化能力和增加的CD4(+)FoxP3(+)T淋巴细胞数量,并抑制了PBMCs的增殖和凋亡。IFN-γ的添加增强了DFSCs的增殖。此外,与其他细胞来源相比,DFSCs抑制了IL-4和IFN-γ细胞因子水平并提高了IL-10水平。结论。这些结果表明,IFN-γ通过对健康供体的PBMCs诱导免疫调节作用来刺激DFSCs,同时抑制凋亡和增殖并增加CD4(+)FoxP3(+)细胞的数量。