Cargando…

Hierarchical patterning modes orchestrate hair follicle morphogenesis

Two theories address the origin of repeating patterns, such as hair follicles, limb digits, and intestinal villi, during development. The Turing reaction–diffusion system posits that interacting diffusible signals produced by static cells first define a prepattern that then induces cell rearrangemen...

Descripción completa

Detalles Bibliográficos
Autores principales: Glover, James D., Wells, Kirsty L., Matthäus, Franziska, Painter, Kevin J., Ho, William, Riddell, Jon, Johansson, Jeanette A., Ford, Matthew J., Jahoda, Colin A. B., Klika, Vaclav, Mort, Richard L., Headon, Denis J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507405/
https://www.ncbi.nlm.nih.gov/pubmed/28700594
http://dx.doi.org/10.1371/journal.pbio.2002117
_version_ 1783249728726630400
author Glover, James D.
Wells, Kirsty L.
Matthäus, Franziska
Painter, Kevin J.
Ho, William
Riddell, Jon
Johansson, Jeanette A.
Ford, Matthew J.
Jahoda, Colin A. B.
Klika, Vaclav
Mort, Richard L.
Headon, Denis J.
author_facet Glover, James D.
Wells, Kirsty L.
Matthäus, Franziska
Painter, Kevin J.
Ho, William
Riddell, Jon
Johansson, Jeanette A.
Ford, Matthew J.
Jahoda, Colin A. B.
Klika, Vaclav
Mort, Richard L.
Headon, Denis J.
author_sort Glover, James D.
collection PubMed
description Two theories address the origin of repeating patterns, such as hair follicles, limb digits, and intestinal villi, during development. The Turing reaction–diffusion system posits that interacting diffusible signals produced by static cells first define a prepattern that then induces cell rearrangements to produce an anatomical structure. The second theory, that of mesenchymal self-organisation, proposes that mobile cells can form periodic patterns of cell aggregates directly, without reference to any prepattern. Early hair follicle development is characterised by the rapid appearance of periodic arrangements of altered gene expression in the epidermis and prominent clustering of the adjacent dermal mesenchymal cells. We assess the contributions and interplay between reaction–diffusion and mesenchymal self-organisation processes in hair follicle patterning, identifying a network of fibroblast growth factor (FGF), wingless-related integration site (WNT), and bone morphogenetic protein (BMP) signalling interactions capable of spontaneously producing a periodic pattern. Using time-lapse imaging, we find that mesenchymal cell condensation at hair follicles is locally directed by an epidermal prepattern. However, imposing this prepattern’s condition of high FGF and low BMP activity across the entire skin reveals a latent dermal capacity to undergo spatially patterned self-organisation in the absence of epithelial direction. This mesenchymal self-organisation relies on restricted transforming growth factor (TGF) β signalling, which serves to drive chemotactic mesenchymal patterning when reaction–diffusion patterning is suppressed, but, in normal conditions, facilitates cell movement to locally prepatterned sources of FGF. This work illustrates a hierarchy of periodic patterning modes operating in organogenesis.
format Online
Article
Text
id pubmed-5507405
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-55074052017-07-25 Hierarchical patterning modes orchestrate hair follicle morphogenesis Glover, James D. Wells, Kirsty L. Matthäus, Franziska Painter, Kevin J. Ho, William Riddell, Jon Johansson, Jeanette A. Ford, Matthew J. Jahoda, Colin A. B. Klika, Vaclav Mort, Richard L. Headon, Denis J. PLoS Biol Research Article Two theories address the origin of repeating patterns, such as hair follicles, limb digits, and intestinal villi, during development. The Turing reaction–diffusion system posits that interacting diffusible signals produced by static cells first define a prepattern that then induces cell rearrangements to produce an anatomical structure. The second theory, that of mesenchymal self-organisation, proposes that mobile cells can form periodic patterns of cell aggregates directly, without reference to any prepattern. Early hair follicle development is characterised by the rapid appearance of periodic arrangements of altered gene expression in the epidermis and prominent clustering of the adjacent dermal mesenchymal cells. We assess the contributions and interplay between reaction–diffusion and mesenchymal self-organisation processes in hair follicle patterning, identifying a network of fibroblast growth factor (FGF), wingless-related integration site (WNT), and bone morphogenetic protein (BMP) signalling interactions capable of spontaneously producing a periodic pattern. Using time-lapse imaging, we find that mesenchymal cell condensation at hair follicles is locally directed by an epidermal prepattern. However, imposing this prepattern’s condition of high FGF and low BMP activity across the entire skin reveals a latent dermal capacity to undergo spatially patterned self-organisation in the absence of epithelial direction. This mesenchymal self-organisation relies on restricted transforming growth factor (TGF) β signalling, which serves to drive chemotactic mesenchymal patterning when reaction–diffusion patterning is suppressed, but, in normal conditions, facilitates cell movement to locally prepatterned sources of FGF. This work illustrates a hierarchy of periodic patterning modes operating in organogenesis. Public Library of Science 2017-07-11 /pmc/articles/PMC5507405/ /pubmed/28700594 http://dx.doi.org/10.1371/journal.pbio.2002117 Text en © 2017 Glover 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Glover, James D.
Wells, Kirsty L.
Matthäus, Franziska
Painter, Kevin J.
Ho, William
Riddell, Jon
Johansson, Jeanette A.
Ford, Matthew J.
Jahoda, Colin A. B.
Klika, Vaclav
Mort, Richard L.
Headon, Denis J.
Hierarchical patterning modes orchestrate hair follicle morphogenesis
title Hierarchical patterning modes orchestrate hair follicle morphogenesis
title_full Hierarchical patterning modes orchestrate hair follicle morphogenesis
title_fullStr Hierarchical patterning modes orchestrate hair follicle morphogenesis
title_full_unstemmed Hierarchical patterning modes orchestrate hair follicle morphogenesis
title_short Hierarchical patterning modes orchestrate hair follicle morphogenesis
title_sort hierarchical patterning modes orchestrate hair follicle morphogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507405/
https://www.ncbi.nlm.nih.gov/pubmed/28700594
http://dx.doi.org/10.1371/journal.pbio.2002117
work_keys_str_mv AT gloverjamesd hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis
AT wellskirstyl hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis
AT matthausfranziska hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis
AT painterkevinj hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis
AT howilliam hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis
AT riddelljon hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis
AT johanssonjeanettea hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis
AT fordmatthewj hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis
AT jahodacolinab hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis
AT klikavaclav hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis
AT mortrichardl hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis
AT headondenisj hierarchicalpatterningmodesorchestratehairfolliclemorphogenesis