Cargando…
Modelling Hair Follicle Growth Dynamics as an Excitable Medium
The hair follicle system represents a tractable model for the study of stem cell behaviour in regenerative adult epithelial tissue. However, although there are numerous spatial scales of observation (molecular, cellular, follicle and multi follicle), it is not yet clear what mechanisms underpin the...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527291/ https://www.ncbi.nlm.nih.gov/pubmed/23284275 http://dx.doi.org/10.1371/journal.pcbi.1002804 |
_version_ | 1782253690556514304 |
---|---|
author | Murray, Philip J. Maini, Philip K. Plikus, Maksim V. Chuong, Cheng-Ming Baker, Ruth E. |
author_facet | Murray, Philip J. Maini, Philip K. Plikus, Maksim V. Chuong, Cheng-Ming Baker, Ruth E. |
author_sort | Murray, Philip J. |
collection | PubMed |
description | The hair follicle system represents a tractable model for the study of stem cell behaviour in regenerative adult epithelial tissue. However, although there are numerous spatial scales of observation (molecular, cellular, follicle and multi follicle), it is not yet clear what mechanisms underpin the follicle growth cycle. In this study we seek to address this problem by describing how the growth dynamics of a large population of follicles can be treated as a classical excitable medium. Defining caricature interactions at the molecular scale and treating a single follicle as a functional unit, a minimal model is proposed in which the follicle growth cycle is an emergent phenomenon. Expressions are derived, in terms of parameters representing molecular regulation, for the time spent in the different functional phases of the cycle, a formalism that allows the model to be directly compared with a previous cellular automaton model and experimental measurements made at the single follicle scale. A multi follicle model is constructed and numerical simulations are used to demonstrate excellent qualitative agreement with a range of experimental observations. Notably, the excitable medium equations exhibit a wider family of solutions than the previous work and we demonstrate how parameter changes representing altered molecular regulation can explain perturbed patterns in Wnt over-expression and BMP down-regulation mouse models. Further experimental scenarios that could be used to test the fundamental premise of the model are suggested. The key conclusion from our work is that positive and negative regulatory interactions between activators and inhibitors can give rise to a range of experimentally observed phenomena at the follicle and multi follicle spatial scales and, as such, could represent a core mechanism underlying hair follicle growth. |
format | Online Article Text |
id | pubmed-3527291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35272912013-01-02 Modelling Hair Follicle Growth Dynamics as an Excitable Medium Murray, Philip J. Maini, Philip K. Plikus, Maksim V. Chuong, Cheng-Ming Baker, Ruth E. PLoS Comput Biol Research Article The hair follicle system represents a tractable model for the study of stem cell behaviour in regenerative adult epithelial tissue. However, although there are numerous spatial scales of observation (molecular, cellular, follicle and multi follicle), it is not yet clear what mechanisms underpin the follicle growth cycle. In this study we seek to address this problem by describing how the growth dynamics of a large population of follicles can be treated as a classical excitable medium. Defining caricature interactions at the molecular scale and treating a single follicle as a functional unit, a minimal model is proposed in which the follicle growth cycle is an emergent phenomenon. Expressions are derived, in terms of parameters representing molecular regulation, for the time spent in the different functional phases of the cycle, a formalism that allows the model to be directly compared with a previous cellular automaton model and experimental measurements made at the single follicle scale. A multi follicle model is constructed and numerical simulations are used to demonstrate excellent qualitative agreement with a range of experimental observations. Notably, the excitable medium equations exhibit a wider family of solutions than the previous work and we demonstrate how parameter changes representing altered molecular regulation can explain perturbed patterns in Wnt over-expression and BMP down-regulation mouse models. Further experimental scenarios that could be used to test the fundamental premise of the model are suggested. The key conclusion from our work is that positive and negative regulatory interactions between activators and inhibitors can give rise to a range of experimentally observed phenomena at the follicle and multi follicle spatial scales and, as such, could represent a core mechanism underlying hair follicle growth. Public Library of Science 2012-12-20 /pmc/articles/PMC3527291/ /pubmed/23284275 http://dx.doi.org/10.1371/journal.pcbi.1002804 Text en © 2012 Murray 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 Murray, Philip J. Maini, Philip K. Plikus, Maksim V. Chuong, Cheng-Ming Baker, Ruth E. Modelling Hair Follicle Growth Dynamics as an Excitable Medium |
title | Modelling Hair Follicle Growth Dynamics as an Excitable Medium |
title_full | Modelling Hair Follicle Growth Dynamics as an Excitable Medium |
title_fullStr | Modelling Hair Follicle Growth Dynamics as an Excitable Medium |
title_full_unstemmed | Modelling Hair Follicle Growth Dynamics as an Excitable Medium |
title_short | Modelling Hair Follicle Growth Dynamics as an Excitable Medium |
title_sort | modelling hair follicle growth dynamics as an excitable medium |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527291/ https://www.ncbi.nlm.nih.gov/pubmed/23284275 http://dx.doi.org/10.1371/journal.pcbi.1002804 |
work_keys_str_mv | AT murrayphilipj modellinghairfolliclegrowthdynamicsasanexcitablemedium AT mainiphilipk modellinghairfolliclegrowthdynamicsasanexcitablemedium AT plikusmaksimv modellinghairfolliclegrowthdynamicsasanexcitablemedium AT chuongchengming modellinghairfolliclegrowthdynamicsasanexcitablemedium AT bakerruthe modellinghairfolliclegrowthdynamicsasanexcitablemedium |