Cargando…

Noise-driven cell differentiation and the emergence of spatiotemporal patterns

The emergence of phenotypic diversity in a population of cells and their arrangement in space and time is one of the most fascinating features of living systems. In fact, understanding multicellularity is unthinkable without explaining the proximate and the ultimate causes of cell differentiation in...

Descripción completa

Detalles Bibliográficos
Autores principales: Safdari, Hadiseh, Kalirad, Ata, Picioreanu, Cristian, Tusserkani, Rouzbeh, Goliaei, Bahram, Sadeghi, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7182191/
https://www.ncbi.nlm.nih.gov/pubmed/32330159
http://dx.doi.org/10.1371/journal.pone.0232060
_version_ 1783526196289470464
author Safdari, Hadiseh
Kalirad, Ata
Picioreanu, Cristian
Tusserkani, Rouzbeh
Goliaei, Bahram
Sadeghi, Mehdi
author_facet Safdari, Hadiseh
Kalirad, Ata
Picioreanu, Cristian
Tusserkani, Rouzbeh
Goliaei, Bahram
Sadeghi, Mehdi
author_sort Safdari, Hadiseh
collection PubMed
description The emergence of phenotypic diversity in a population of cells and their arrangement in space and time is one of the most fascinating features of living systems. In fact, understanding multicellularity is unthinkable without explaining the proximate and the ultimate causes of cell differentiation in time and space. Simpler forms of cell differentiation can be found in unicellular organisms, such as bacterial biofilm, where reversible cell differentiation results in phenotypically diverse populations. In this manuscript, we attempt to start with the simple case of reversible nongenetic phenotypic to construct a model of differentiation and pattern formation. Our model, which we refer to as noise-driven differentiation (NDD) model, is an attempt to consider the prevalence of noise in biological systems, alongside what is known about genetic switches and signaling, to create a simple model which generates spatiotemporal patterns from bottom-up. Our simulations indicate that the presence of noise in cells can lead to reversible differentiation and the addition of signaling can create spatiotemporal pattern.
format Online
Article
Text
id pubmed-7182191
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-71821912020-05-05 Noise-driven cell differentiation and the emergence of spatiotemporal patterns Safdari, Hadiseh Kalirad, Ata Picioreanu, Cristian Tusserkani, Rouzbeh Goliaei, Bahram Sadeghi, Mehdi PLoS One Research Article The emergence of phenotypic diversity in a population of cells and their arrangement in space and time is one of the most fascinating features of living systems. In fact, understanding multicellularity is unthinkable without explaining the proximate and the ultimate causes of cell differentiation in time and space. Simpler forms of cell differentiation can be found in unicellular organisms, such as bacterial biofilm, where reversible cell differentiation results in phenotypically diverse populations. In this manuscript, we attempt to start with the simple case of reversible nongenetic phenotypic to construct a model of differentiation and pattern formation. Our model, which we refer to as noise-driven differentiation (NDD) model, is an attempt to consider the prevalence of noise in biological systems, alongside what is known about genetic switches and signaling, to create a simple model which generates spatiotemporal patterns from bottom-up. Our simulations indicate that the presence of noise in cells can lead to reversible differentiation and the addition of signaling can create spatiotemporal pattern. Public Library of Science 2020-04-24 /pmc/articles/PMC7182191/ /pubmed/32330159 http://dx.doi.org/10.1371/journal.pone.0232060 Text en © 2020 Safdari 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
Safdari, Hadiseh
Kalirad, Ata
Picioreanu, Cristian
Tusserkani, Rouzbeh
Goliaei, Bahram
Sadeghi, Mehdi
Noise-driven cell differentiation and the emergence of spatiotemporal patterns
title Noise-driven cell differentiation and the emergence of spatiotemporal patterns
title_full Noise-driven cell differentiation and the emergence of spatiotemporal patterns
title_fullStr Noise-driven cell differentiation and the emergence of spatiotemporal patterns
title_full_unstemmed Noise-driven cell differentiation and the emergence of spatiotemporal patterns
title_short Noise-driven cell differentiation and the emergence of spatiotemporal patterns
title_sort noise-driven cell differentiation and the emergence of spatiotemporal patterns
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7182191/
https://www.ncbi.nlm.nih.gov/pubmed/32330159
http://dx.doi.org/10.1371/journal.pone.0232060
work_keys_str_mv AT safdarihadiseh noisedrivencelldifferentiationandtheemergenceofspatiotemporalpatterns
AT kaliradata noisedrivencelldifferentiationandtheemergenceofspatiotemporalpatterns
AT picioreanucristian noisedrivencelldifferentiationandtheemergenceofspatiotemporalpatterns
AT tusserkanirouzbeh noisedrivencelldifferentiationandtheemergenceofspatiotemporalpatterns
AT goliaeibahram noisedrivencelldifferentiationandtheemergenceofspatiotemporalpatterns
AT sadeghimehdi noisedrivencelldifferentiationandtheemergenceofspatiotemporalpatterns