Yokose Satoshi, Kadokura Hiroshi, Tajima Naoto, Hasegawa Akihiko, Sakagami Hiroshi, Fujieda Kazuo, Katayama Tadashi
Department of Operative Dentistry, School of Dentistry, Meikai University, 1-1 Keyakidai, Sakado, 350-0283 Saitama, Japan.
Cell Tissue Res. 2004 Mar;315(3):375-84. doi: 10.1007/s00441-003-0839-5. Epub 2004 Jan 22.
Platelet-derived growth factor (PDGF) has recently been demonstrated to control the expression of alkaline phosphatase and proteoglycan synthesis of odontoblastic cells in dental pulp tissues. Although PDGF appears to be closely related to dentinogenesis, much about the mode of action of PDGF on odontoblast differentiation remains unclear. In this study, we examined the effects of three PDGF dimers (PDGF AA, AB, and BB) on odontoblastic differentiation of dental pulp cells in long-term mineralized cultures. Dental pulp cells isolated from rat lower incisors were continuously treated with each of PDGF AA, AB, and BB in separate cultures for 20 days. The three PDGF dimers suppressed alkaline phosphatase activity, osteocalcin and calcium content, and the formation of dentin-like nodules. The expression of mRNA for dentin sialoprotein (DSP) in the cells was inhibited by PDGF AA treatment, whereas PDGF AB and BB treatment stimulated the expression of DSP, even though the dentin-like nodule formation was inhibited. Although the effects of PDGF on odontoblastic differentiation varied among the dimers, the cells expressed both PDGF alpha and beta receptors, whose quantities were similar. These results suggest that PDGF exerts diverse effects on odontoblastic differentiation depending on its dimeric form. These in vitro findings explain, at least in part, the in vivo action of PDGF in dentinogenesis during the repair process of damaged dental pulp.
血小板衍生生长因子(PDGF)最近已被证明可控制牙髓组织中牙本质细胞碱性磷酸酶的表达和蛋白聚糖的合成。尽管PDGF似乎与牙本质形成密切相关,但关于PDGF对成牙本质细胞分化的作用方式仍不清楚。在本研究中,我们检测了三种PDGF二聚体(PDGF AA、AB和BB)对长期矿化培养的牙髓细胞成牙本质细胞分化的影响。从大鼠下切牙分离的牙髓细胞在单独培养中分别用PDGF AA、AB和BB连续处理20天。三种PDGF二聚体均抑制碱性磷酸酶活性、骨钙素和钙含量以及牙本质样结节的形成。PDGF AA处理抑制了细胞中牙本质涎蛋白(DSP)的mRNA表达,而PDGF AB和BB处理则刺激了DSP的表达,尽管牙本质样结节的形成受到抑制。虽然PDGF对成牙本质细胞分化的影响在二聚体之间有所不同,但细胞同时表达了PDGFα和β受体,其数量相似。这些结果表明,PDGF根据其二聚体形式对成牙本质细胞分化产生不同的影响。这些体外研究结果至少部分解释了PDGF在受损牙髓修复过程中牙本质形成中的体内作用。