Department of Pulp Biology and Endodontics, Graduate School of Kanagawa Dental University, Yokosuka, Japan.
Oral Microbiology, Graduate School of Kanagawa Dental University, Yokosuka, Japan.
J Endod. 2021 Apr;47(4):606-611. doi: 10.1016/j.joen.2020.12.019. Epub 2021 Jan 9.
Transforming growth factor beta 1 (TGF-β1) plays an important role in bone mineralization and has been reported to promote osteoblast proliferation and differentiation. However, there is no report about the effects of TGF-β1 on human cementoblasts. The purpose of this study was to clarify the effect of TGF-β1 on the proliferation and differentiation of the human cementoblast cell line (HCEM) in vitro.
HCEM cells were stimulated with TGF-β1 at concentrations of 0.05, 0.5, 5, and 10 ng/mL. A proliferation assay was performed from 24-72 hours. The effect of TGF-β1 on mineralization was analyzed by quantifying the area stained with alizarin red on days 7 and 14. Real-time polymerase chain reaction was used to assess the effect of TGF-β1 on the mineralization-related genes alkaline phosphatase, bone sialoprotein, and type I collagen on days 3, 7, and 14.
TGF-β1 did not affect cell proliferation. TGF-β1 together with the mineralization medium (consisting of ascorbic acid, dexamethasone, and β-glycerophosphate) increased the alizarin red-stained area on days 7 and 14. Real-time polymerase chain reaction revealed that alkaline phosphatase messenger RNA expression was increased in TGF-β1-stimulated HCEM cells in mineralization medium on days 3 and 7, whereas bone sialoprotein and type I collagen messenger RNA expression was increased on day 7.
Although TGF-β1 does not affect cell proliferation, it does promote cell differentiation and mineralization of HCEM cells.
转化生长因子-β1(TGF-β1)在骨矿化中起着重要作用,据报道它能促进成骨细胞增殖和分化。然而,目前尚无关于 TGF-β1 对人牙骨质细胞影响的报道。本研究旨在阐明 TGF-β1 对人牙骨质细胞系(HCEM)体外增殖和分化的影响。
用浓度为 0.05、0.5、5 和 10ng/ml 的 TGF-β1 刺激 HCEM 细胞。在 24-72 小时进行增殖测定。通过定量茜素红染色区域分析 TGF-β1 对第 7 天和第 14 天的矿化作用。用实时聚合酶链反应评估 TGF-β1 对碱性磷酸酶、骨涎蛋白和 I 型胶原等矿化相关基因在第 3、7 和 14 天的影响。
TGF-β1 不影响细胞增殖。TGF-β1 与矿化培养基(含抗坏血酸、地塞米松和β-甘油磷酸)一起作用,增加了第 7 天和第 14 天茜素红染色区域。实时聚合酶链反应显示,矿化培养基中 TGF-β1 刺激的 HCEM 细胞中碱性磷酸酶信使 RNA 表达在第 3 天和第 7 天增加,而骨涎蛋白和 I 型胶原信使 RNA 表达在第 7 天增加。
尽管 TGF-β1 不影响细胞增殖,但它确实促进了 HCEM 细胞的分化和矿化。