Literature DB >> 12057916

E- and N-cadherin distribution in developing and functional human teeth under normal and pathological conditions.

Robert Heymann1, Imad About, Urban Lendahl, Jean-Claude Franquin, Björn Obrink, Thimios A Mitsiadis.   

Abstract

Cadherins are calcium-dependent cell adhesion molecules involved in the regulation of various biological processes such as cell recognition, intercellular communication, cell fate, cell polarity, boundary formation, and morphogenesis. Although previous studies have shown E-cadherin expression during rodent or human odontogenesis, there is no equivalent study available on N-cadherin expression in dental tissues. Here we examined and compared the expression patterns of E- and N-cadherins in both embryonic and adult (healthy, injured, carious) human teeth. Both proteins were expressed in the developing teeth during the cap and bell stages. E-cadherin expression in dental epithelium followed an apical-coronal gradient that was opposite to that observed for N-cadherin. E-cadherin was distributed in proliferating cells of the inner and outer enamel epithelia but not in differentiated cells such as ameloblasts, whereas N-cadherin expression was up-regulated in differentiated epithelial cells. By contrast to E-cadherin, N-cadherin was also expressed in mesenchymal cells that differentiate into odontoblasts and produce the hard tissue matrix of dentin. Although N-cadherin was not detected in permanent intact teeth, it was re-expressed during dentin repair processes in odontoblasts surrounding carious or traumatic sites. Similarly, N-cadherin re-expression was seen in vitro, in cultured primary pulp cells that differentiate into odontoblast-like cells. Taken together these results suggest that E- and N-cadherins may play a role during human tooth development and, moreover, indicate that N-cadherin is important for odontoblast function in normal development and under pathological conditions.

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Year:  2002        PMID: 12057916      PMCID: PMC1850842          DOI: 10.1016/S0002-9440(10)61161-3

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  61 in total

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  25 in total

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Journal:  Am J Pathol       Date:  2011-05       Impact factor: 4.307

4.  FGF controls epithelial-mesenchymal transitions during gastrulation by regulating cell division and apicobasal polarity.

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Journal:  Development       Date:  2018-10-01       Impact factor: 6.868

5.  Matrix metalloproteinase 20 promotes a smooth enamel surface, a strong dentino-enamel junction, and a decussating enamel rod pattern.

Authors:  John D Bartlett; Ziedonis Skobe; Antonio Nanci; Charles E Smith
Journal:  Eur J Oral Sci       Date:  2011-12       Impact factor: 2.612

Review 6.  Modulation of cell-cell junctional complexes by matrix metalloproteinases.

Authors:  J D Bartlett; C E Smith
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7.  Chromosomal protein HMGN1 modulates the expression of N-cadherin.

Authors:  Yaffa R Rubinstein; Takashi Furusawa; Jae-Hwan Lim; Yuri V Postnikov; Katherine L West; Yehudit Birger; Sunmin Lee; Phuongmai Nguyen; Jane B Trepel; Michael Bustin
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8.  Immortalization of normal human gingival keratinocytes and cytological and cytogenetic characterization of the cells.

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10.  Epigenetic marks define the lineage and differentiation potential of two distinct neural crest-derived intermediate odontogenic progenitor populations.

Authors:  Gokul Gopinathan; Antonia Kolokythas; Xianghong Luan; Thomas G H Diekwisch
Journal:  Stem Cells Dev       Date:  2013-03-15       Impact factor: 3.272

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