Nakamura Takashi, Chiba Yuta, Naruse Masahiro, Saito Kan, Harada Hidemitsu, Fukumoto Satoshi
Division of Molecular Pharmacology and Cell Biophysics, Department of Oral Biology, Tohoku University Graduate School of Dentistry, Sendai, Japan.
Division of Pediatric Dentistry, Department of Oral Health and Development Sciences, Tohoku University Graduate School of Dentistry, Sendai, Japan.
Int J Oral Sci. 2016 Dec 16;8(4):205-212. doi: 10.1038/ijos.2016.35.
Tooth crown morphogenesis is tightly regulated by the proliferation and differentiation of dental epithelial cells. Globoside (Gb4), a globo-series glycosphingolipid, is highly expressed during embryogenesis as well as organogenesis, including tooth development. We previously reported that Gb4 is dominantly expressed in the neutral lipid fraction of dental epithelial cells. However, because its functional role in tooth development remains unknown, we investigated the involvement of Gb4 in dental epithelial cell differentiation. The expression of Gb4 was detected in ameloblasts of postnatal mouse molars and incisors. A cell culture analysis using HAT-7 cells, a rat-derived dental epithelial cell line, revealed that Gb4 did not promote dental epithelial cell proliferation. Interestingly, exogenous administration of Gb4 enhanced the gene expression of enamel extracellular matrix proteins such as ameloblastin, amelogenin, and enamelin in dental epithelial cells as well as in developing tooth germs. Gb4 also induced the expression of TrkB, one of the key receptors required for ameloblast induction in dental epithelial cells. In contrast, Gb4 downregulated the expression of p75, a receptor for neurotrophins (including neurotrophin-4) and a marker of undifferentiated dental epithelial cells. In addition, we found that exogenous administration of Gb4 to dental epithelial cells stimulated the extracellular signal-regulated kinase and p38 mitogen-activated protein kinase signalling pathways. Furthermore, Gb4 induced the expression of epiprofin and Runx2, the positive regulators for ameloblastin gene transcription. Thus, our results suggest that Gb4 contributes to promoting the differentiation of dental epithelial cells into ameloblasts.
牙冠形态发生受牙上皮细胞增殖和分化的严格调控。红细胞糖苷脂(Gb4)是一种球系列糖鞘脂,在胚胎发生以及包括牙齿发育在内的器官发生过程中高度表达。我们之前报道Gb4主要在牙上皮细胞的中性脂质部分表达。然而,由于其在牙齿发育中的功能作用尚不清楚,我们研究了Gb4在牙上皮细胞分化中的作用。在出生后小鼠磨牙和切牙的成釉细胞中检测到了Gb4的表达。使用大鼠来源的牙上皮细胞系HAT-7细胞进行的细胞培养分析表明,Gb4不促进牙上皮细胞增殖。有趣的是,外源性给予Gb4可增强牙上皮细胞以及发育中的牙胚中釉质细胞外基质蛋白如成釉蛋白、釉原蛋白和釉蛋白的基因表达。Gb4还诱导了TrkB的表达,TrkB是牙上皮细胞中诱导成釉细胞所需的关键受体之一。相反,Gb4下调了p75的表达,p75是神经营养因子(包括神经营养因子-4)的受体,也是未分化牙上皮细胞的标志物。此外,我们发现外源性给予牙上皮细胞Gb4可刺激细胞外信号调节激酶和p38丝裂原活化蛋白激酶信号通路。此外,Gb4诱导了epiprofin和Runx2的表达,它们是成釉蛋白基因转录的正调节因子。因此,我们的结果表明Gb4有助于促进牙上皮细胞分化为成釉细胞。