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A Model for Cell Proliferation in a Developing Organism
In mathematical biology, there is a great deal of interest in producing continuum models by scaling discrete agent-based models governed by local stochastic rules. We discuss a particular example of this approach: a model for the proliferation of neural crest cells that can help us understand the de...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233659/ https://www.ncbi.nlm.nih.gov/pubmed/35752652 http://dx.doi.org/10.1007/s00285-022-01769-5 |
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author | Pollett, Philip K. Tafakori, Laleh Taylor, Peter G. |
author_facet | Pollett, Philip K. Tafakori, Laleh Taylor, Peter G. |
author_sort | Pollett, Philip K. |
collection | PubMed |
description | In mathematical biology, there is a great deal of interest in producing continuum models by scaling discrete agent-based models governed by local stochastic rules. We discuss a particular example of this approach: a model for the proliferation of neural crest cells that can help us understand the development of Hirschprung’s disease, a potentially-fatal condition in which the enteric nervous system of a new-born child does not extend all the way through the intestine and colon. Our starting point is a discrete-state, continuous-time Markov chain model proposed by Hywood et al. (2013a) for the location of the neural crest cells that make up the enteric nervous system. Hywood et al. (2013a) scaled their model to derive an approximate second order partial differential equation describing how the limiting expected number of neural crest cells evolve in space and time. In contrast, we exploit the relationship between the above-mentioned Markov chain model and the well-known Yule-Furry process to derive the exact form of the scaled version of the process. Furthermore, we provide expressions for other features of the domain agent occupancy process, such as the variance of the marginal occupancy at a particular site, the distribution of the number of agents that are yet to reach a given site and a stochastic description of the process itself. |
format | Online Article Text |
id | pubmed-9233659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-92336592022-06-27 A Model for Cell Proliferation in a Developing Organism Pollett, Philip K. Tafakori, Laleh Taylor, Peter G. J Math Biol Article In mathematical biology, there is a great deal of interest in producing continuum models by scaling discrete agent-based models governed by local stochastic rules. We discuss a particular example of this approach: a model for the proliferation of neural crest cells that can help us understand the development of Hirschprung’s disease, a potentially-fatal condition in which the enteric nervous system of a new-born child does not extend all the way through the intestine and colon. Our starting point is a discrete-state, continuous-time Markov chain model proposed by Hywood et al. (2013a) for the location of the neural crest cells that make up the enteric nervous system. Hywood et al. (2013a) scaled their model to derive an approximate second order partial differential equation describing how the limiting expected number of neural crest cells evolve in space and time. In contrast, we exploit the relationship between the above-mentioned Markov chain model and the well-known Yule-Furry process to derive the exact form of the scaled version of the process. Furthermore, we provide expressions for other features of the domain agent occupancy process, such as the variance of the marginal occupancy at a particular site, the distribution of the number of agents that are yet to reach a given site and a stochastic description of the process itself. Springer Berlin Heidelberg 2022-06-25 2022 /pmc/articles/PMC9233659/ /pubmed/35752652 http://dx.doi.org/10.1007/s00285-022-01769-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Pollett, Philip K. Tafakori, Laleh Taylor, Peter G. A Model for Cell Proliferation in a Developing Organism |
title | A Model for Cell Proliferation in a Developing Organism |
title_full | A Model for Cell Proliferation in a Developing Organism |
title_fullStr | A Model for Cell Proliferation in a Developing Organism |
title_full_unstemmed | A Model for Cell Proliferation in a Developing Organism |
title_short | A Model for Cell Proliferation in a Developing Organism |
title_sort | model for cell proliferation in a developing organism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233659/ https://www.ncbi.nlm.nih.gov/pubmed/35752652 http://dx.doi.org/10.1007/s00285-022-01769-5 |
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