Fibroblast growth factor signalling regulates the development of tooth root

Author:

Jin Chengxue12ORCID,Adachi Noritaka1ORCID,Yoshimoto Yuki1ORCID,Sasabuchi Aino1ORCID,Kawashima Nobuyuki3ORCID,Ota Masato S.4ORCID,Iseki Sachiko1ORCID

Affiliation:

1. Department of Molecular Craniofacial Embryology and Oral Histology, Graduate School of Medical and Dental Sciences Tokyo Medical and Dental University (TMDU) Tokyo Japan

2. Department of Oral, Plastic and Aesthetic Surgery, Hospital of Stomatology Jilin University Changchun Jilin China

3. Department of Pulp Biology and Endodontics, Graduate School of Medical and Dental Sciences Tokyo Medical and Dental University (TMDU) Tokyo Japan

4. Laboratory of Anatomy, Physiology and Food Biological Science, Department of Food and Nutrition, Faculty of Human Sciences and Design Japan Women's University Tokyo Japan

Abstract

AbstractFibroblast growth factor (FGF) signalling plays a crucial role in the morphogenesis of multiple tissues including teeth. While the role of the signal has been studied in tooth crown development, little is known about root development. Of several FGF ligands involved in hard tissue formation, we suggest that FGF18 regulates the development of murine tooth roots. We implanted FGF18‐soaked heparin beads into the lower first molar tooth buds at postnatal day 6 (P6), followed by transplantation under the kidney capsule. After 3 weeks, FGF18 significantly facilitated root elongation and periodontal tissue formation compared to the control. In situ hybridisation showed that Fgf18 transcripts were initially localised in the dental pulp along Hertwig's epithelial root sheath at P6 and P10 and subsequently in the dental follicle cells at P14. Fgf receptors were expressed in various dental tissues during these stages. In vitro analysis using the dental pulp stem cells revealed that FGF18 inhibited cell proliferation and decreased expression levels of osteogenic markers, Runx2, Alpl and Sp7. Consistently, after 1 week of kidney capsule transplantation, FGF18 application did not induce the expression of Sp7 and Bsp, but upregulated Periostin in the apical region of dental mesenchyme in the grafted molar. These findings suggest that FGF18 facilitates molar root development by regulating the calcification of periodontal tissues.

Publisher

Wiley

Subject

Cell Biology,Developmental Biology,Molecular Biology,Ecology, Evolution, Behavior and Systematics,Histology,Anatomy

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