School of Dental Sciences, Universiti Sains Malaysia, 16150, Kubang Kerian, Kelantan, Malaysia.
School of Dental Sciences, Universiti Sains Malaysia, 16150, Kubang Kerian, Kelantan, Malaysia; Human Genome Centre, School of Medical Sciences, Universiti Sains Malaysia, 16150, Kubang Kerian, Kelantan, Malaysia.
J Craniomaxillofac Surg. 2018 Aug;46(8):1361-1367. doi: 10.1016/j.jcms.2018.05.002. Epub 2018 May 9.
In this study, we evaluated the potential role of IL-6 and/or IL-17A in regulating the OPG/RANKL (osteoprotegerin/receptor activator of nuclear factor kappa b ligand) system of murine osteoblast cell line (MC3T3-E1) cultured on hydroxyapatite (HA).
MC3T3-E1 cells were seeded on HA and treated with recombinant IL-6 or rIL-17A or combination of the two cytokines. Cell proliferation and differentiation activity were measured by MTS and alkaline phosphatase assays respectively. Observation of cell adhesion and proliferation was examined by scanning electron microscopy. Gene and protein expressions were performed on RANKL and OPG using qPCR, Western blot and ELISA.
We demonstrated that treatment with recombinant IL-17A (rIL-17A) and the combination rIL-6/rIL-17A promoted better adhesion and higher proliferation of cells on HA. Cells treated with rIL-17A and the combination cytokines showed a significant increase in differentiation activity on day 7, 10 and 14 as indicated by ALP activity (p < 0.001). Gene and protein expressions showed significant up-regulation of OPG and ALP (p < 0.001) and down-regulation of RANKL (p < 0.001) expression by all the treated groups. Interestingly, the combination of the two cytokines resulted in a significant increase of OPG/RANKL ratio (p < 0.001).
These findings indicated that treatment with the combination of the two cytokines (IL-6/IL-17A) has synergistic effects to promote osteoblastic differentiation but suppress osteoclastogenesis by altering the OPG/RANKL ratio.
本研究旨在评估白细胞介素 6(IL-6)和/或白细胞介素 17A(IL-17A)在调节培养于羟基磷灰石(HA)上的鼠成骨细胞系(MC3T3-E1)的 OPG/RANKL(骨保护素/核因子 κB 受体激活剂配体)系统中的潜在作用。
将 MC3T3-E1 细胞接种于 HA 上,并分别用重组白细胞介素 6(rIL-6)或 rIL-17A 或两种细胞因子的组合处理。通过 MTS 和碱性磷酸酶测定分别测量细胞增殖和分化活性。通过扫描电子显微镜观察细胞黏附和增殖情况。使用 qPCR、Western blot 和 ELISA 检测 RANKL 和 OPG 的基因和蛋白表达。
我们证明,用重组白细胞介素 17A(rIL-17A)和 rIL-6/rIL-17A 联合处理可促进细胞在 HA 上更好地黏附和增殖。用 rIL-17A 和联合细胞因子处理的细胞在第 7、10 和 14 天的分化活性显著增加,碱性磷酸酶活性显著升高(p<0.001)。基因和蛋白表达显示,所有处理组均显著上调 OPG 和 ALP(p<0.001)表达,并下调 RANKL(p<0.001)表达。有趣的是,两种细胞因子的联合处理导致 OPG/RANKL 比值显著增加(p<0.001)。
这些发现表明,两种细胞因子(IL-6/IL-17A)的联合治疗具有协同作用,可通过改变 OPG/RANKL 比值促进成骨细胞分化,但抑制破骨细胞生成。