Sagomonyants K, Kalajzic I, Maye P, Mina M
1 Department of Oral Health and Diagnostic Sciences, School of Dental Medicine, University of Connecticut Health Center, Farmington, CT, USA.
2 Department of Reconstructive Sciences, School of Dental Medicine, University of Connecticut Health Center, Farmington, CT, USA.
J Dent Res. 2017 Jun;96(6):663-670. doi: 10.1177/0022034517691732. Epub 2017 Feb 7.
Members of the fibroblast growth factor (FGF) family play essential and important roles in primary and reparative dentinogenesis, with conflicting results regarding their effects on odontoblast differentiation. Our recent studies showed that the effects of FGF2 on cells in odontoblast lineage were stage-specific and depended on the stage of cell maturity. Continuous exposure of pulp cells to FGF2 inhibited odontoblast differentiation, whereas early and limited exposure of pulp cells to FGF2 resulted in marked increases in odontoblast differentiation. The purpose of this study was to evaluate the cellular and molecular mechanisms regulating the inhibitory effects of FGF2 on odontoblast differentiation. To do so, we examined the effects of the addition of FGF2 during the differentiation/mineralization phase of the in vitro growth of pulp cultures derived from a series of green fluorescent protein reporter transgenic mice that display stage-specific activation of transgenes during odontoblast differentiation. Our results showed that this treatment first stimulated the differentiation of remaining progenitors in pulp cultures into functional odontoblasts but prevented their differentiation into mature odontoblasts. In addition, this treatment inhibited expression of markers of osteogenesis. Furthermore, we demonstrated that the inhibitory effects of FGF2 on odontoblast differentiation were mediated through activation of FGFR/MEK/Erk1/2 signaling and downregulation of bone morphogenetic protein signaling, with negative and positive roles in the expression of Dmp1 and Dspp, respectively, during the advanced stage of odontoblast differentiation.
成纤维细胞生长因子(FGF)家族成员在原发性和修复性牙本质形成过程中发挥着至关重要的作用,但其对成牙本质细胞分化的影响却存在相互矛盾的结果。我们最近的研究表明,FGF2对成牙本质细胞谱系中的细胞的影响具有阶段特异性,并且取决于细胞成熟的阶段。牙髓细胞持续暴露于FGF2会抑制成牙本质细胞分化,而牙髓细胞早期和有限地暴露于FGF2会导致成牙本质细胞分化显著增加。本研究的目的是评估调节FGF2对成牙本质细胞分化抑制作用的细胞和分子机制。为此,我们在源自一系列绿色荧光蛋白报告转基因小鼠的牙髓培养物的体外生长的分化/矿化阶段添加FGF2,这些转基因小鼠在成牙本质细胞分化过程中显示出转基因的阶段特异性激活。我们的结果表明,这种处理首先刺激了牙髓培养物中剩余祖细胞分化为功能性成牙本质细胞,但阻止了它们分化为成熟的成牙本质细胞。此外,这种处理抑制了成骨标志物的表达。此外,我们证明FGF2对成牙本质细胞分化的抑制作用是通过激活FGFR/MEK/Erk1/2信号传导和下调骨形态发生蛋白信号传导介导的,在成牙本质细胞分化的晚期阶段,分别对Dmp1和Dspp的表达起负向和正向作用。