Laboratory for the Study of Regenerative Dental Medicine, Department of Oral Histology-Developmental Biology, School of Dentistry and Dental Research Institute, Seoul National University, 1 Gwanakro, Gwanak-gu, Seoul, 08826, Republic of Korea.
Department of Dental Hygiene, Seoyeong University, Gwang-ju, Republic of Korea.
J Mol Histol. 2019 Jun;50(3):179-188. doi: 10.1007/s10735-019-09816-0. Epub 2019 Mar 12.
Interactions between the ectodermal and mesenchymal tissues are the basis of the central mechanism regulating tooth development. Based on this epithelial-mesenchymal interaction (EMI), we demonstrated that copine-7 (CPNE7) is secreted by preameloblasts and regulates the differentiation of mesenchymal cells of dental or non-dental origin into odontoblasts. However, the precise expression patterns of CPNE7 in the stages of tooth development have not yet been elucidated. The aim of the present study was to establish the spatiotemporal expression pattern of CPNE7 during mouse tooth development. To examine the spatiotemporal expression patterns of CPNE7 during mouse tooth development, we investigate the distribution of CPNE7 in the embryonic and postnatal developing mouse tooth. Immunohistochemistry, in situ hybridization, real-time PCR, and western blot analysis are performed to investigate the CPNE7 expression pattern during tooth development of the mandibular mouse first molar. During the initiation stage (bud stage), CPNE7 protein expression is observed in the dental epithelium but not yet in the dental mesenchyme. At E18 (bell stage), expression of CPNE7 protein and mRNA is primarily observed in ectomesenchymal cells of dental papilla. At P7 (crown formation stage), CPNE7 is localized in differentiating odontoblasts but weak expression is detected in mature ameloblasts. These findings suggest that CPNE7 secreted by dental epithelium induces the differentiation of ectomesenchymal cells into preodontoblast in concert with EMI. CPNE7 is clearly expressed in differentiating odontoblasts and the odontoblast process during dentinogenesis, but is no longer expressed in fully differentiated odontoblasts. Furthermore, CPNE7 is expressed in the Hertwig's epithelial root sheath (HERS) and in the facing preodontoblasts during root dentin formation. Taken together, these results illustrate the dynamic expression of CPNE7 during tooth development and suggest its important function in entire stages of tooth development.
外胚层和中胚层组织之间的相互作用是调节牙齿发育的中央机制的基础。基于这种上皮-间质相互作用(EMI),我们证明了 copine-7(CPNE7)由前成釉细胞分泌,并调节牙源性或非牙源性中胚层细胞向成牙本质细胞的分化。然而,CPNE7 在牙齿发育阶段的精确表达模式尚未阐明。本研究旨在建立 CPNE7 在小鼠牙齿发育过程中的时空表达模式。为了研究 CPNE7 在小鼠牙齿发育过程中的时空表达模式,我们研究了 CPNE7 在胚胎和出生后发育的小鼠牙齿中的分布。通过免疫组织化学、原位杂交、实时 PCR 和 Western blot 分析,研究了下颌第一磨牙小鼠牙齿发育过程中 CPNE7 的表达模式。在启动阶段(芽状期),在牙上皮中观察到 CPNE7 蛋白表达,但在牙间质中尚未观察到。在 E18(钟状期),CPNE7 蛋白和 mRNA 的表达主要观察到在牙乳头的外胚间充质细胞中。在 P7(牙冠形成期),CPNE7 定位于分化的成牙本质细胞中,但在成熟的成釉细胞中检测到弱表达。这些发现表明,牙上皮分泌的 CPNE7 与 EMI 一起诱导外胚间充质细胞分化为前成牙本质细胞。CPNE7 在牙本质形成过程中在分化的成牙本质细胞和成牙本质细胞突起中明显表达,但在完全分化的成牙本质细胞中不再表达。此外,CPNE7 在 Hertwig 的上皮根鞘(HERS)和面向的前成牙本质细胞中表达,用于根牙本质形成。综上所述,这些结果说明了 CPNE7 在牙齿发育过程中的动态表达,并表明其在牙齿发育的整个阶段都具有重要的功能。