Copine-7 binds to the cell surface receptor, nucleolin, and regulates ciliogenesis and Dspp expression during odontoblast differentiation

• Published in: Scientific reports Vol. 7; no. 1; pp. 11283 - 13
• Main Authors: Seo, You-Mi, Park, Su-Jin, Lee, Hye-Kyung, Park, Joo-Cheol
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 12.09.2017; Nature Publishing Group
• Subjects: 14/19; 38/77; 38/89; 38/90; 42/109; 631/80/86; 692/698/1671; 82/58; 82/80; Calcium; Caveolae; Cell Differentiation - genetics; Cell surface; Cilia - metabolism; Dental pulp; Endocytosis; Epithelium; Extracellular Matrix Proteins - genetics; Gene Expression Regulation; Humanities and Social Sciences; Humans; Internalization; Membrane Proteins - metabolism; Mesenchyme; multidisciplinary; Nucleolin; Odontoblasts; Odontoblasts - cytology; Odontoblasts - metabolism; Odontogenesis; Phosphoproteins - genetics; Phosphoproteins - metabolism; Protein Transport; Proteins; RNA-Binding Proteins - metabolism; Science; Science (multidisciplinary); Sialoglycoproteins - genetics; siRNA; Teeth
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-017-11641-y

Tooth development is a progressive process regulated by interactions between epithelial and mesenchymal tissues. Our previous studies showed that copine-7 (Cpne7), a dental epithelium-derived protein, is a signalling molecule that is secreted by preameloblasts and regulates the differentiation of preodontoblasts into odontoblasts. However, the mechanisms involved in the translocation of Cpne7 from preameloblasts to preodontoblasts and the functions of Cpne7 during odontogenesis are poorly understood. Here, we showed that the internalization of Cpne7 was mediated primarily by caveolae. This process was initiated by Cpne7 binding to the cell surface protein, nucleolin. Treatment with recombinant Cpne7 protein (rCpne7) in human dental pulp cells (hDPCs) caused an increase in the number of ciliated cells. The expression level of cilium components, Ift88 and Kif3a, and Dspp were increased by rCpne7. Treatment with Ift88 siRNA in hDPCs and MDPC-23 cells significantly down-regulated the expression of Dspp, an odontoblastic differentiation marker gene. Furthermore, the treatment with nucleolin siRNA in MDPC-23 cells decreased the expression of Dmp1, Dspp, and cilium components. Our findings suggested that the binding of Cpne7 with its receptor, nucleolin, has an important function involving Cpne7 internalization into preodontoblasts and regulation of Dspp expression through ciliogenesis during odontoblast differentiation.