Fibulin-1 Regulates Initiation of Successional Dental Lamina

Author:

Li G.123,Li Q.12,Shen Z.12,Lin X.12ORCID,Li X.45,Wang J.12,Zhao B.12,Feng Y.12,Feng L.12,Guo W.12,Hu L.12,Wang J.125,Zhang C.12,Fan Z.12,Wang S.1246,Wu X.145

Affiliation:

1. Beijing Laboratory of Oral Health, Capital Medical University, Beijing, China

2. Molecular Laboratory of Gene Therapy and Tooth Regeneration, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction, Capital Medical University School of Stomatology, Beijing, China

3. Department of Dental Implantology, Affiliated Hospital of Stomatology, Nanjing Medical University, Nanjing, Jiangsu, China

4. Academician Workstation for Oral-Maxillofacial Regenerative Medicine, Central South University, Changsha, China

5. Department of Oral and Maxillofacial Surgery, Xiangya Hospital, Central South University, Changsha, China

6. Department of Biochemistry and Molecular Biology, Capital Medical University School of Basic Medical Sciences, Beijing, China

Abstract

In humans, teeth are replaced only once, and the successional dental lamina (SDL) of the permanent tooth is maintained in a quiescent state until adolescence. Recently, we showed that biomechanical stress generated by the rapid growth of the deciduous tooth inhibits SDL development via integrin β1–RUNX2 signaling at embryonic day 60 (E60) in miniature pigs. However, the mechanism by which RUNX2 regulates SDL initiation within the SDL stem cell niche remains unclear. In the current study, we transcriptionally profiled single cells from SDL and surrounding mesenchyme at E60 and identified the landscape of cellular heterogeneity. We then identified a specific fibroblast subtype in the dental follicle mesenchyme between the deciduous tooth and the SDL of the permanent tooth (DFDP), which constitutes the inner part of the niche (deciduous tooth side). Compared with traditional dental follicle cells, the specific expression profile of DFDP was identified and found to be related to biomechanical stress. Subsequently, we found that RUNX2 could bind to the enhancer regions of Fbln1 (gene of fibulin-1), one of the marker genes for DFDP. Through gain- and loss-of-function experiments, we proved that the biomechanical stress–mediated RUNX2–fibulin-1 axis inhibits the initiation of SDL by maintaining SDL niche homeostasis.

Publisher

SAGE Publications

Subject

General Dentistry

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