Department of Orofacial Sciences, University of California-San Francisco, 521 Parnassus Avenue, San Francisco, CA 94143-0640, USA.
Matrix Biol. 2010 Jun;29(5):411-9. doi: 10.1016/j.matbio.2010.03.001. Epub 2010 Mar 6.
Tooth enamel is formed by epithelially-derived cells called ameloblasts, while the pulp dentin complex is formed by the dental mesenchyme. These tissues differentiate with reciprocal signaling interactions to form a mature tooth. In this study we have characterized ameloblast differentiation in human developing incisors, and have further investigated the role of extracellular matrix proteins on ameloblast differentiation. Histological and immunohistochemical analyses showed that in the human tooth, the basement membrane separating the early developing dental epithelium and mesenchyme was lost shortly before dentin deposition was initiated, prior to enamel matrix secretion. Presecretary ameloblasts elongated as they came into contact with the dentin matrix, and then shortened to become secretory ameloblasts. In situ hybridization showed that the presecretory stage of odontoblasts started to express type I collagen mRNA, and also briefly expressed amelogenin mRNA. This was followed by upregulation of amelogenin mRNA expression in secretory ameloblasts. In vitro, amelogenin expression was upregulated in ameloblast lineage cells cultured in Matrigel, and was further up-regulated when these cells/Matrigel were co-cultured with dental pulp cells. Co-culture also up-regulated type I collagen expression by the dental pulp cells. Type I collagen coated culture dishes promoted a more elongated ameloblast lineage cell morphology and enhanced cell adhesion via integrin alpha2beta1. Taken together, these results suggest that the basement membrane proteins and signals from underlying mesenchymal cells coordinate to initiate differentiation of preameloblasts and regulate type I collagen expression by odontoblasts. Type I collagen in the dentin matrix then anchors the presecretary ameloblasts as they further differentiate to secretory cells. These studies show the critical roles of the extracellular matrix proteins in ameloblast differentiation.
牙釉质是由称为成釉细胞的上皮细胞衍生而来的,而牙髓牙本质复合体则由牙间质形成。这些组织通过相互信号传递来分化,形成成熟的牙齿。在本研究中,我们对人类发育中切牙的成釉细胞分化进行了描述,并进一步研究了细胞外基质蛋白对成釉细胞分化的作用。组织学和免疫组织化学分析表明,在人类牙齿中,在牙本质沉积开始之前,即在釉质基质分泌之前,分隔早期发育的牙上皮和间质的基膜很快丢失。前分泌期成釉细胞在与牙本质基质接触时伸长,然后缩短成为分泌期成釉细胞。原位杂交显示,成牙本质细胞的前分泌期开始表达 I 型胶原 mRNA,并且短暂地表达釉原蛋白 mRNA。随后,分泌期成釉细胞中釉原蛋白 mRNA 的表达上调。在体外,在 Matrigel 中培养的成釉细胞系中,釉原蛋白表达上调,当这些细胞/Matrigel 与牙髓细胞共培养时,其表达进一步上调。共培养还上调了牙髓细胞的 I 型胶原表达。I 型胶原包被的培养皿促进了更细长的成釉细胞系细胞形态,并通过整合素 α2β1 增强细胞黏附。总之,这些结果表明,基膜蛋白和来自下方间质细胞的信号共同启动前成釉细胞的分化,并调节成牙本质细胞的 I 型胶原表达。牙本质基质中的 I 型胶原随后固定进一步分化为分泌细胞的前分泌期成釉细胞。这些研究表明细胞外基质蛋白在成釉细胞分化中起着关键作用。