Division of Oral Health, Growth and Development, Faculty of Dental Science, Kyushu University, Fukuoka, Japan.
Arch Oral Biol. 2010 Jun;55(6):426-34. doi: 10.1016/j.archoralbio.2010.03.011. Epub 2010 Apr 14.
The purpose of this study was to elucidate the effects of platelet-derived growth factors (PDGFs) during tooth development, as well as the mechanisms underlying the interactions of growth factors with PDGF signalling during odontogenesis.
We used an ex vivo tooth germ organ culture system and two dental cell lines, SF2 cells and mDP cells, as models of odontogenesis. AG17, a tyrosine kinase inhibitor, was utilised for blocking PDGF receptor signalling. To analyse the expressions of PDGFs, reverse transcriptase (RT)-PCR and immunohistochemistry were performed. Proliferation was examined using a BrdU incorporation assay for the organ cultures and a cell counting kit for the cell lines. The expressions of Fgf2 and ameloblastin were analysed by real-time RT-PCR.
The PDGF ligands PDGF-A and PDGF-B, and their receptors, PDGFRalpha and PDGFRbeta, were expressed throughout the initial stages of tooth development. In the tooth germ organ cultures, PDGF-AA, but not PDGF-BB, accelerated cusp formation. Conversely, AG17 suppressed both growth and cusp formation of tooth germs. Exogenous PDGF-BB promoted mDP cell proliferation. Furthermore, PDGF-AA decreased Fgf2 expression and increased that of ameloblastin, a marker of differentiated ameloblasts.
Our results indicate that PDGFs are involved in initial tooth development and regulate tooth size and shape, as well as ameloblast differentiation.
本研究旨在阐明血小板衍生生长因子(PDGFs)在牙齿发育过程中的作用,以及生长因子与牙发生过程中 PDGF 信号相互作用的机制。
我们使用了离体牙胚器官培养系统和两个牙细胞系,SF2 细胞和 mDP 细胞,作为牙发生的模型。AG17,一种酪氨酸激酶抑制剂,用于阻断 PDGF 受体信号。为了分析 PDGFs 的表达,进行了逆转录(RT)-PCR 和免疫组织化学分析。通过器官培养的 BrdU 掺入测定和细胞系的细胞计数试剂盒来检测增殖。通过实时 RT-PCR 分析 Fgf2 和釉原蛋白的表达。
PDGF 配体 PDGF-A 和 PDGF-B 及其受体 PDGFRalpha 和 PDGFRbeta 在牙齿发育的初始阶段表达。在牙胚器官培养物中,PDGF-AA 而非 PDGF-BB 加速了牙尖的形成。相反,AG17 抑制了牙胚的生长和牙尖的形成。外源性 PDGF-BB 促进了 mDP 细胞的增殖。此外,PDGF-AA 降低了 Fgf2 的表达,增加了分化成釉细胞的标志物釉原蛋白的表达。
我们的结果表明,PDGFs 参与了牙齿的初始发育,调节牙齿的大小和形状,以及成釉细胞的分化。