Washio Ayako, Kitamura Chiaki, Morotomi Takahiko, Terashita Masamichi, Nishihara Tatsuji
Division of Pulp Biology, Operative Dentistry, and Endodontics, Department of Cariology and Periodontology, Kyushu Dental College, Kitakyushu, Japan.
Int J Dent. 2012;2012:258469. doi: 10.1155/2012/258469. Epub 2012 Feb 28.
We examined the effects of bone morphogenetic protein-2 (BMP-2) on growth, differentiation, and intracellular signaling pathways of odontoblast-like cells, KN-3 cells, to clarify molecular mechanisms of odontoblast differentiation during pulp regeneration process. After treatment with BMP-2, the cell morphology, growth, alkaline phosphatase (ALP) activity, and the activation and expression of BMP-induced intracellular signaling molecules, such as Smad1/5/8 and Smad6/7, as well as activities of dentin sialoprotein (DSP) and dentin matrix protein 1 (DMP1), were examined. BMP-2 had no effects on the morphology, growth, or ALP activity of KN-3 cells, whereas it induced the phosphorylation of Smad1/5/8 and expression of Smad6/7. BMP-2 also induced the expressions of DSP and DMP-1. Our results suggest that KN-3 cells may express an odontoblastic phenotype with the addition of BMP-2 through the activation of Smad signaling pathways.
我们研究了骨形态发生蛋白-2(BMP-2)对成牙本质样细胞KN-3细胞生长、分化及细胞内信号通路的影响,以阐明牙髓再生过程中成牙本质细胞分化的分子机制。用BMP-2处理后,检测细胞形态、生长、碱性磷酸酶(ALP)活性,以及BMP诱导的细胞内信号分子如Smad1/5/8和Smad6/7的激活与表达,还有牙本质涎蛋白(DSP)和牙本质基质蛋白1(DMP1)的活性。BMP-2对KN-3细胞的形态、生长或ALP活性无影响,却能诱导Smad1/5/8磷酸化及Smad6/7表达。BMP-2还能诱导DSP和DMP-1的表达。我们的结果表明,添加BMP-2后,KN-3细胞可能通过激活Smad信号通路表达成牙本质细胞表型。