Cargando…
Epithelial stratification and placode invagination are separable functions in early morphogenesis of the molar tooth
Ectodermal organs, which include teeth, hair follicles, mammary ducts, and glands such as sweat, mucous and sebaceous glands, are initiated in development as placodes, which are epithelial thickenings that invaginate and bud into the underlying mesenchyme. These placodes are stratified into a basal...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760321/ https://www.ncbi.nlm.nih.gov/pubmed/26755699 http://dx.doi.org/10.1242/dev.130187 |
_version_ | 1782416859049492480 |
---|---|
author | Li, Jingjing Chatzeli, Lemonia Panousopoulou, Eleni Tucker, Abigail S. Green, Jeremy B. A. |
author_facet | Li, Jingjing Chatzeli, Lemonia Panousopoulou, Eleni Tucker, Abigail S. Green, Jeremy B. A. |
author_sort | Li, Jingjing |
collection | PubMed |
description | Ectodermal organs, which include teeth, hair follicles, mammary ducts, and glands such as sweat, mucous and sebaceous glands, are initiated in development as placodes, which are epithelial thickenings that invaginate and bud into the underlying mesenchyme. These placodes are stratified into a basal and several suprabasal layers of cells. The mechanisms driving stratification and invagination are poorly understood. Using the mouse molar tooth as a model for ectodermal organ morphogenesis, we show here that vertical, stratifying cell divisions are enriched in the forming placode and that stratification is cell division dependent. Using inhibitor and gain-of-function experiments, we show that FGF signalling is necessary and sufficient for stratification but not invagination as such. We show that, instead, Shh signalling is necessary for, and promotes, invagination once suprabasal tissue is generated. Shh-dependent suprabasal cell shape suggests convergent migration and intercalation, potentially accounting for post-stratification placode invagination to bud stage. We present a model in which FGF generates suprabasal tissue by asymmetric cell division, while Shh triggers cell rearrangement in this tissue to drive invagination all the way to bud formation. |
format | Online Article Text |
id | pubmed-4760321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47603212016-03-04 Epithelial stratification and placode invagination are separable functions in early morphogenesis of the molar tooth Li, Jingjing Chatzeli, Lemonia Panousopoulou, Eleni Tucker, Abigail S. Green, Jeremy B. A. Development Research Article Ectodermal organs, which include teeth, hair follicles, mammary ducts, and glands such as sweat, mucous and sebaceous glands, are initiated in development as placodes, which are epithelial thickenings that invaginate and bud into the underlying mesenchyme. These placodes are stratified into a basal and several suprabasal layers of cells. The mechanisms driving stratification and invagination are poorly understood. Using the mouse molar tooth as a model for ectodermal organ morphogenesis, we show here that vertical, stratifying cell divisions are enriched in the forming placode and that stratification is cell division dependent. Using inhibitor and gain-of-function experiments, we show that FGF signalling is necessary and sufficient for stratification but not invagination as such. We show that, instead, Shh signalling is necessary for, and promotes, invagination once suprabasal tissue is generated. Shh-dependent suprabasal cell shape suggests convergent migration and intercalation, potentially accounting for post-stratification placode invagination to bud stage. We present a model in which FGF generates suprabasal tissue by asymmetric cell division, while Shh triggers cell rearrangement in this tissue to drive invagination all the way to bud formation. The Company of Biologists Ltd 2016-02-15 /pmc/articles/PMC4760321/ /pubmed/26755699 http://dx.doi.org/10.1242/dev.130187 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Li, Jingjing Chatzeli, Lemonia Panousopoulou, Eleni Tucker, Abigail S. Green, Jeremy B. A. Epithelial stratification and placode invagination are separable functions in early morphogenesis of the molar tooth |
title | Epithelial stratification and placode invagination are separable functions in early morphogenesis of the molar tooth |
title_full | Epithelial stratification and placode invagination are separable functions in early morphogenesis of the molar tooth |
title_fullStr | Epithelial stratification and placode invagination are separable functions in early morphogenesis of the molar tooth |
title_full_unstemmed | Epithelial stratification and placode invagination are separable functions in early morphogenesis of the molar tooth |
title_short | Epithelial stratification and placode invagination are separable functions in early morphogenesis of the molar tooth |
title_sort | epithelial stratification and placode invagination are separable functions in early morphogenesis of the molar tooth |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760321/ https://www.ncbi.nlm.nih.gov/pubmed/26755699 http://dx.doi.org/10.1242/dev.130187 |
work_keys_str_mv | AT lijingjing epithelialstratificationandplacodeinvaginationareseparablefunctionsinearlymorphogenesisofthemolartooth AT chatzelilemonia epithelialstratificationandplacodeinvaginationareseparablefunctionsinearlymorphogenesisofthemolartooth AT panousopouloueleni epithelialstratificationandplacodeinvaginationareseparablefunctionsinearlymorphogenesisofthemolartooth AT tuckerabigails epithelialstratificationandplacodeinvaginationareseparablefunctionsinearlymorphogenesisofthemolartooth AT greenjeremyba epithelialstratificationandplacodeinvaginationareseparablefunctionsinearlymorphogenesisofthemolartooth |