Department of Oral Histology-Developmental Biology, School of Dentistry and Dental Research Institute, BK 21, Seoul National University, Seoul 110-749, Republic of Korea.
Department of Oral and Maxillofacial Surgery, School of Dentistry, Seoul National University, Seoul 110-749, Republic of Korea.
Biomaterials. 2015 Jan;37:208-17. doi: 10.1016/j.biomaterials.2014.10.016. Epub 2014 Oct 19.
Tooth development involves sequential interactions between dental epithelial and mesenchymal cells. Our previous studies demonstrated that preameloblast-conditioned medium (PA-CM) induces the odontogenic differentiation of human dental pulp cells (hDPCs), and the novel protein Cpne7 in PA-CM was suggested as a candidate signaling molecule. In the present study, we investigated biological function and mechanisms of Cpne7 in regulation of odontoblast differentiation. Cpne7 was expressed in preameloblasts and secreted extracellularly during ameloblast differentiation. After secretion, Cpne7 protein was translocated to differentiating odontoblasts. In odontoblasts, Cpne7 promoted odontoblastic markers and the expression of Dspp in vitro. Cpne7 also induced odontoblast differentiation and promoted dentin/pulp-like tissue formation in hDPCs in vivo. Moreover, Cpne7 induced differentiation into odontoblasts of non-dental mesenchymal stem cells in vitro, and promoted formation of dentin-like tissues including the structure of dentinal tubules in vivo. Mechanistically, Cpne7 interacted with Nucleolin and modulated odontoblast differentiation via the control of Dspp expression. These results suggest Cpne7 is a diffusible signaling molecule that is secreted by preameloblasts, and regulates the differentiation of mesenchymal cells of dental or non-dental origin into odontoblasts.
牙齿发育涉及牙上皮细胞和间充质细胞之间的顺序相互作用。我们之前的研究表明,前成釉细胞条件培养基(PA-CM)诱导人牙髓细胞(hDPC)的牙源性分化,而 PA-CM 中的新型蛋白 Cpne7 被认为是候选信号分子。在本研究中,我们研究了 Cpne7 在调节成牙本质细胞分化中的生物学功能和机制。Cpne7 在成釉细胞前体细胞中表达,并在成釉细胞分化过程中外泌到细胞外。分泌后,Cpne7 蛋白易位到分化的成牙本质细胞中。在成牙本质细胞中,Cpne7 体外促进成牙本质标志物和 Dspp 的表达。Cpne7 还诱导 hDPC 体内的成牙本质细胞分化,并促进牙本质/牙髓样组织的形成。此外,Cpne7 在体外诱导非牙源性间充质干细胞分化为成牙本质细胞,并促进包括牙本质小管结构在内的牙本质样组织的形成。在机制上,Cpne7 与核仁蛋白相互作用,并通过控制 Dspp 的表达来调节成牙本质细胞的分化。这些结果表明 Cpne7 是一种可扩散的信号分子,由前成釉细胞分泌,并调节牙源性或非牙源性间充质细胞向成牙本质细胞的分化。