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Interaction between Fibronectin and β1 Integrin Is Essential for Tooth Development

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 d...

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Autores principales: Saito, Kan, Fukumoto, Emiko, Yamada, Aya, Yuasa, Kenji, Yoshizaki, Keigo, Iwamoto, Tsutomu, Saito, Masahiro, Nakamura, Takashi, Fukumoto, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382024/
https://www.ncbi.nlm.nih.gov/pubmed/25830530
http://dx.doi.org/10.1371/journal.pone.0121667
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author Saito, Kan
Fukumoto, Emiko
Yamada, Aya
Yuasa, Kenji
Yoshizaki, Keigo
Iwamoto, Tsutomu
Saito, Masahiro
Nakamura, Takashi
Fukumoto, Satoshi
author_facet Saito, Kan
Fukumoto, Emiko
Yamada, Aya
Yuasa, Kenji
Yoshizaki, Keigo
Iwamoto, Tsutomu
Saito, Masahiro
Nakamura, Takashi
Fukumoto, Satoshi
author_sort Saito, Kan
collection PubMed
description 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 (Intβ1(lox-/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.
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spelling pubmed-43820242015-04-09 Interaction between Fibronectin and β1 Integrin Is Essential for Tooth Development Saito, Kan Fukumoto, Emiko Yamada, Aya Yuasa, Kenji Yoshizaki, Keigo Iwamoto, Tsutomu Saito, Masahiro Nakamura, Takashi Fukumoto, Satoshi PLoS One Research Article 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 (Intβ1(lox-/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. Public Library of Science 2015-04-01 /pmc/articles/PMC4382024/ /pubmed/25830530 http://dx.doi.org/10.1371/journal.pone.0121667 Text en © 2015 Saito et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Saito, Kan
Fukumoto, Emiko
Yamada, Aya
Yuasa, Kenji
Yoshizaki, Keigo
Iwamoto, Tsutomu
Saito, Masahiro
Nakamura, Takashi
Fukumoto, Satoshi
Interaction between Fibronectin and β1 Integrin Is Essential for Tooth Development
title Interaction between Fibronectin and β1 Integrin Is Essential for Tooth Development
title_full Interaction between Fibronectin and β1 Integrin Is Essential for Tooth Development
title_fullStr Interaction between Fibronectin and β1 Integrin Is Essential for Tooth Development
title_full_unstemmed Interaction between Fibronectin and β1 Integrin Is Essential for Tooth Development
title_short Interaction between Fibronectin and β1 Integrin Is Essential for Tooth Development
title_sort interaction between fibronectin and β1 integrin is essential for tooth development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382024/
https://www.ncbi.nlm.nih.gov/pubmed/25830530
http://dx.doi.org/10.1371/journal.pone.0121667
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