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Skin Stem Cell Hypotheses and Long Term Clone Survival – Explored Using Agent-based Modelling
Epithelial renewal in skin is achieved by the constant turnover and differentiation of keratinocytes. Three popular hypotheses have been proposed to explain basal keratinocyte regeneration and epidermal homeostasis: 1) asymmetric division (stem-transit amplifying cell); 2) populational asymmetry (pr...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664904/ https://www.ncbi.nlm.nih.gov/pubmed/23712735 http://dx.doi.org/10.1038/srep01904 |
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author | Li, X. Upadhyay, A. K. Bullock, A. J. Dicolandrea, T. Xu, J. Binder, R. L. Robinson, M. K. Finlay, D. R. Mills, K. J. Bascom, C. C. Kelling, C. K. Isfort, R. J. Haycock, J. W. MacNeil, S. Smallwood, R. H. |
author_facet | Li, X. Upadhyay, A. K. Bullock, A. J. Dicolandrea, T. Xu, J. Binder, R. L. Robinson, M. K. Finlay, D. R. Mills, K. J. Bascom, C. C. Kelling, C. K. Isfort, R. J. Haycock, J. W. MacNeil, S. Smallwood, R. H. |
author_sort | Li, X. |
collection | PubMed |
description | Epithelial renewal in skin is achieved by the constant turnover and differentiation of keratinocytes. Three popular hypotheses have been proposed to explain basal keratinocyte regeneration and epidermal homeostasis: 1) asymmetric division (stem-transit amplifying cell); 2) populational asymmetry (progenitor cell with stochastic fate); and 3) populational asymmetry with stem cells. In this study, we investigated lineage dynamics using these hypotheses with a 3D agent-based model of the epidermis. The model simulated the growth and maintenance of the epidermis over three years. The offspring of each proliferative cell was traced. While all lineages were preserved in asymmetric division, the vast majority were lost when assuming populational asymmetry. The third hypothesis provided the most reliable mechanism for self-renewal by preserving genetic heterogeneity in quiescent stem cells, and also inherent mechanisms for skin ageing and the accumulation of genetic mutation. |
format | Online Article Text |
id | pubmed-3664904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-36649042013-05-28 Skin Stem Cell Hypotheses and Long Term Clone Survival – Explored Using Agent-based Modelling Li, X. Upadhyay, A. K. Bullock, A. J. Dicolandrea, T. Xu, J. Binder, R. L. Robinson, M. K. Finlay, D. R. Mills, K. J. Bascom, C. C. Kelling, C. K. Isfort, R. J. Haycock, J. W. MacNeil, S. Smallwood, R. H. Sci Rep Article Epithelial renewal in skin is achieved by the constant turnover and differentiation of keratinocytes. Three popular hypotheses have been proposed to explain basal keratinocyte regeneration and epidermal homeostasis: 1) asymmetric division (stem-transit amplifying cell); 2) populational asymmetry (progenitor cell with stochastic fate); and 3) populational asymmetry with stem cells. In this study, we investigated lineage dynamics using these hypotheses with a 3D agent-based model of the epidermis. The model simulated the growth and maintenance of the epidermis over three years. The offspring of each proliferative cell was traced. While all lineages were preserved in asymmetric division, the vast majority were lost when assuming populational asymmetry. The third hypothesis provided the most reliable mechanism for self-renewal by preserving genetic heterogeneity in quiescent stem cells, and also inherent mechanisms for skin ageing and the accumulation of genetic mutation. Nature Publishing Group 2013-05-28 /pmc/articles/PMC3664904/ /pubmed/23712735 http://dx.doi.org/10.1038/srep01904 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Li, X. Upadhyay, A. K. Bullock, A. J. Dicolandrea, T. Xu, J. Binder, R. L. Robinson, M. K. Finlay, D. R. Mills, K. J. Bascom, C. C. Kelling, C. K. Isfort, R. J. Haycock, J. W. MacNeil, S. Smallwood, R. H. Skin Stem Cell Hypotheses and Long Term Clone Survival – Explored Using Agent-based Modelling |
title | Skin Stem Cell Hypotheses and Long Term Clone Survival – Explored Using Agent-based Modelling |
title_full | Skin Stem Cell Hypotheses and Long Term Clone Survival – Explored Using Agent-based Modelling |
title_fullStr | Skin Stem Cell Hypotheses and Long Term Clone Survival – Explored Using Agent-based Modelling |
title_full_unstemmed | Skin Stem Cell Hypotheses and Long Term Clone Survival – Explored Using Agent-based Modelling |
title_short | Skin Stem Cell Hypotheses and Long Term Clone Survival – Explored Using Agent-based Modelling |
title_sort | skin stem cell hypotheses and long term clone survival – explored using agent-based modelling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664904/ https://www.ncbi.nlm.nih.gov/pubmed/23712735 http://dx.doi.org/10.1038/srep01904 |
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