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Spatial signalling mediated by the transforming growth factor-β signalling pathway during tooth formation

Tooth development relies on sequential and reciprocal interactions between the epithelial and mesenchymal tissues, and it is continuously regulated by a variety of conserved and specific temporal-spatial signalling pathways. It is well known that suspensions of tooth germ cells can form tooth-like s...

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Autores principales: He, Xin-Yu, Sun, Ke, Xu, Ruo-Shi, Tan, Jia-Li, Pi, Cai-Xia, Wan, Mian, Peng, Yi-Ran, Ye, Ling, Zheng, Li-Wei, Zhou, Xue-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168420/
https://www.ncbi.nlm.nih.gov/pubmed/27982023
http://dx.doi.org/10.1038/ijos.2016.45
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author He, Xin-Yu
Sun, Ke
Xu, Ruo-Shi
Tan, Jia-Li
Pi, Cai-Xia
Wan, Mian
Peng, Yi-Ran
Ye, Ling
Zheng, Li-Wei
Zhou, Xue-Dong
author_facet He, Xin-Yu
Sun, Ke
Xu, Ruo-Shi
Tan, Jia-Li
Pi, Cai-Xia
Wan, Mian
Peng, Yi-Ran
Ye, Ling
Zheng, Li-Wei
Zhou, Xue-Dong
author_sort He, Xin-Yu
collection PubMed
description Tooth development relies on sequential and reciprocal interactions between the epithelial and mesenchymal tissues, and it is continuously regulated by a variety of conserved and specific temporal-spatial signalling pathways. It is well known that suspensions of tooth germ cells can form tooth-like structures after losing the positional information provided by the epithelial and mesenchymal tissues. However, the particular stage in which the tooth germ cells start to form tooth-like structures after losing their positional information remains unclear. In this study, we investigated the reassociation of tooth germ cells suspension from different morphological stages during tooth development and the phosphorylation of Smad2/3 in this process. Four tooth morphological stages were designed in this study. The results showed that tooth germ cells formed odontogenic tissue at embryonic day (E) 14.5, which is referred to as the cap stage, and they formed tooth-like structures at E16.5, which is referred to as the early bell stage, and E18.5, which is referred to as the late bell stage. Moreover, the transforming growth factor-β signalling pathway might play a role in this process.
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spelling pubmed-51684202016-12-21 Spatial signalling mediated by the transforming growth factor-β signalling pathway during tooth formation He, Xin-Yu Sun, Ke Xu, Ruo-Shi Tan, Jia-Li Pi, Cai-Xia Wan, Mian Peng, Yi-Ran Ye, Ling Zheng, Li-Wei Zhou, Xue-Dong Int J Oral Sci Original Article Tooth development relies on sequential and reciprocal interactions between the epithelial and mesenchymal tissues, and it is continuously regulated by a variety of conserved and specific temporal-spatial signalling pathways. It is well known that suspensions of tooth germ cells can form tooth-like structures after losing the positional information provided by the epithelial and mesenchymal tissues. However, the particular stage in which the tooth germ cells start to form tooth-like structures after losing their positional information remains unclear. In this study, we investigated the reassociation of tooth germ cells suspension from different morphological stages during tooth development and the phosphorylation of Smad2/3 in this process. Four tooth morphological stages were designed in this study. The results showed that tooth germ cells formed odontogenic tissue at embryonic day (E) 14.5, which is referred to as the cap stage, and they formed tooth-like structures at E16.5, which is referred to as the early bell stage, and E18.5, which is referred to as the late bell stage. Moreover, the transforming growth factor-β signalling pathway might play a role in this process. Nature Publishing Group 2016-12 2016-12-16 /pmc/articles/PMC5168420/ /pubmed/27982023 http://dx.doi.org/10.1038/ijos.2016.45 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
He, Xin-Yu
Sun, Ke
Xu, Ruo-Shi
Tan, Jia-Li
Pi, Cai-Xia
Wan, Mian
Peng, Yi-Ran
Ye, Ling
Zheng, Li-Wei
Zhou, Xue-Dong
Spatial signalling mediated by the transforming growth factor-β signalling pathway during tooth formation
title Spatial signalling mediated by the transforming growth factor-β signalling pathway during tooth formation
title_full Spatial signalling mediated by the transforming growth factor-β signalling pathway during tooth formation
title_fullStr Spatial signalling mediated by the transforming growth factor-β signalling pathway during tooth formation
title_full_unstemmed Spatial signalling mediated by the transforming growth factor-β signalling pathway during tooth formation
title_short Spatial signalling mediated by the transforming growth factor-β signalling pathway during tooth formation
title_sort spatial signalling mediated by the transforming growth factor-β signalling pathway during tooth formation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168420/
https://www.ncbi.nlm.nih.gov/pubmed/27982023
http://dx.doi.org/10.1038/ijos.2016.45
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