E-cadherin can replace N-cadherin during secretory-stage enamel development

PLoS One. 2014 Jul 11;9(7):e102153. doi: 10.1371/journal.pone.0102153. eCollection 2014.


Background: N-cadherin is a cell-cell adhesion molecule and deletion of N-cadherin in mice is embryonic lethal. During the secretory stage of enamel development, E-cadherin is down-regulated and N-cadherin is specifically up-regulated in ameloblasts when groups of ameloblasts slide by one another to form the rodent decussating enamel rod pattern. Since N-cadherin promotes cell migration, we asked if N-cadherin is essential for ameloblast cell movement during enamel development.

Methodology/principal findings: The enamel organ, including its ameloblasts, is an epithelial tissue and for this study a mouse strain with N-cadherin ablated from epithelium was generated. Enamel from wild-type (WT) and N-cadherin conditional knockout (cKO) mice was analyzed. μCT and scanning electron microscopy showed that thickness, surface structure, and prism pattern of the cKO enamel looked identical to WT. No significant difference in hardness was observed between WT and cKO enamel. Interestingly, immunohistochemistry revealed the WT and N-cadherin cKO secretory stage ameloblasts expressed approximately equal amounts of total cadherins. Strikingly, E-cadherin was not normally down-regulated during the secretory stage in the cKO mice suggesting that E-cadherin can compensate for the loss of N-cadherin. Previously it was demonstrated that bone morphogenetic protein-2 (BMP2) induces E- and N-cadherin expression in human calvaria osteoblasts and we show that the N-cadherin cKO enamel organ expressed significantly more BMP2 and significantly less of the BMP antagonist Noggin than did WT enamel organ.

Conclusions/significance: The E- to N-cadherin switch at the secretory stage is not essential for enamel development or for forming the decussating enamel rod pattern. E-cadherin can substitute for N-cadherin during these developmental processes. Bmp2 expression may compensate for the loss of N-cadherin by inducing or maintaining E-cadherin expression when E-cadherin is normally down-regulated. Notably, this is the first demonstration of a natural endogenous increase in E-cadherin expression due to N-cadherin ablation in a healthy developing tissue.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Ameloblasts / cytology
  • Ameloblasts / metabolism*
  • Amelogenesis / genetics*
  • Animals
  • Bone Morphogenetic Protein 2 / genetics
  • Bone Morphogenetic Protein 2 / metabolism
  • Cadherins / deficiency
  • Cadherins / genetics*
  • Cadherins / metabolism
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cell Movement
  • Dental Enamel / cytology
  • Dental Enamel / growth & development
  • Dental Enamel / metabolism*
  • Enamel Organ / cytology
  • Enamel Organ / growth & development
  • Enamel Organ / metabolism*
  • Gene Expression Regulation, Developmental
  • Hardness
  • Mice
  • Mice, Knockout
  • Microscopy, Electron, Scanning
  • Primary Cell Culture
  • Signal Transduction
  • Surface Properties


  • Bmp2 protein, mouse
  • Bone Morphogenetic Protein 2
  • Cadherins
  • Carrier Proteins
  • Cdh2 protein, mouse
  • noggin protein