Interaction between fibronectin and β1 integrin is essential for tooth development

PLoS One. 2015 Apr 1;10(4):e0121667. doi: 10.1371/journal.pone.0121667. eCollection 2015.

Abstract

The dental epithelium and extracellular matrix interact to ensure that cell growth and differentiation lead to the formation of teeth of appropriate size and quality. To determine the role of fibronectin in differentiation of the dental epithelium and tooth formation, we analyzed its expression in developing incisors. Fibronectin mRNA was expressed during the presecretory stage in developing dental epithelium, decreased in the secretory and early maturation stages, and then reappeared during the late maturation stage. The binding of dental epithelial cells derived from postnatal day-1 molars to a fibronectin-coated dish was inhibited by the RGD but not RAD peptide, and by a β1 integrin-neutralizing antibody, suggesting that fibronectin-β1 integrin interactions contribute to dental epithelial-cell binding. Because fibronectin and β1 integrin are highly expressed in the dental mesenchyme, it is difficult to determine precisely how their interactions influence dental epithelial differentiation in vivo. Therefore, we analyzed β1 integrin conditional knockout mice (Intβ1lox-/lox-/K14-Cre) and found that they exhibited partial enamel hypoplasia, and delayed eruption of molars and differentiation of ameloblasts, but not of odontoblasts. Furthermore, a cyst-like structure was observed during late ameloblast maturation. Dental epithelial cells from knockout mice did not bind to fibronectin, and induction of ameloblastin expression in these cells by neurotrophic factor-4 was inhibited by treatment with RGD peptide or a fibronectin siRNA, suggesting that the epithelial interaction between fibronectin and β1 integrin is important for ameloblast differentiation and enamel formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion
  • Cell Differentiation
  • Cell Line
  • Collagen Type IV / metabolism
  • Dental Enamel Proteins / metabolism
  • Epithelium / growth & development
  • Epithelium / metabolism
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Fibronectins / genetics
  • Fibronectins / metabolism*
  • Gene Expression
  • Gene Expression Regulation, Developmental
  • Incisor / cytology
  • Incisor / growth & development*
  • Incisor / metabolism
  • Integrin beta1 / metabolism*
  • Laminin / metabolism
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Molar / cytology
  • Molar / growth & development*
  • Molar / metabolism
  • Nerve Growth Factors / metabolism
  • Phosphorylation
  • Protein Processing, Post-Translational
  • Rats

Substances

  • Ambn protein, mouse
  • Collagen Type IV
  • Dental Enamel Proteins
  • Fibronectins
  • Integrin beta1
  • Lamb1 protein, mouse
  • Laminin
  • Nerve Growth Factors
  • Extracellular Signal-Regulated MAP Kinases
  • neurotrophin 4

Grants and funding

This work was supported by Grants-in-Aid from the Ministry of Education, Science (20679006), Culture of Japan, and the NEXT program (LS010), Grant-in-Aid for Young Scientists (24792294), Grant-in-Aid for Scientific Research (21792054). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.