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Sources of variability in cytosolic calcium transients triggered by stimulation of homogeneous uro-epithelial cell monolayers
Epithelial tissue structure is the emergent outcome of the interactions between large numbers of individual cells. Experimental cell biology offers an important tool to unravel these complex interactions, but current methods of analysis tend to be limited to mean field approaches or representation b...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387530/ https://www.ncbi.nlm.nih.gov/pubmed/25694543 http://dx.doi.org/10.1098/rsif.2014.1403 |
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author | Appleby, Peter A. Shabir, Saqib Southgate, Jennifer Walker, Dawn |
author_facet | Appleby, Peter A. Shabir, Saqib Southgate, Jennifer Walker, Dawn |
author_sort | Appleby, Peter A. |
collection | PubMed |
description | Epithelial tissue structure is the emergent outcome of the interactions between large numbers of individual cells. Experimental cell biology offers an important tool to unravel these complex interactions, but current methods of analysis tend to be limited to mean field approaches or representation by selected subsets of cells. This may result in bias towards cells that respond in a particular way and/or neglect local, context-specific cell responses. Here, an automated algorithm was applied to examine in detail the individual calcium transients evoked in genetically homogeneous, but asynchronous populations of cultured non-immortalized normal human urothelial cells when subjected to either the global application of an external agonist or a localized scratch wound. The recorded calcium transients were classified automatically according to a set of defined metrics and distinct sub-populations of cells that responded in qualitatively different ways were observed. The nature of this variability in the homogeneous cell population was apportioned to two sources: intrinsic variation in individual cell responses and extrinsic variability due to context-specific factors of the environment, such as spatial heterogeneity. Statistically significant variation in the features of the calcium transients evoked by scratch wounding according to proximity to the wound edge was identified. The manifestation of distinct sub-populations of cells is considered central to the coordination of population-level response resulting in wound closure. |
format | Online Article Text |
id | pubmed-4387530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-43875302015-04-16 Sources of variability in cytosolic calcium transients triggered by stimulation of homogeneous uro-epithelial cell monolayers Appleby, Peter A. Shabir, Saqib Southgate, Jennifer Walker, Dawn J R Soc Interface Research Articles Epithelial tissue structure is the emergent outcome of the interactions between large numbers of individual cells. Experimental cell biology offers an important tool to unravel these complex interactions, but current methods of analysis tend to be limited to mean field approaches or representation by selected subsets of cells. This may result in bias towards cells that respond in a particular way and/or neglect local, context-specific cell responses. Here, an automated algorithm was applied to examine in detail the individual calcium transients evoked in genetically homogeneous, but asynchronous populations of cultured non-immortalized normal human urothelial cells when subjected to either the global application of an external agonist or a localized scratch wound. The recorded calcium transients were classified automatically according to a set of defined metrics and distinct sub-populations of cells that responded in qualitatively different ways were observed. The nature of this variability in the homogeneous cell population was apportioned to two sources: intrinsic variation in individual cell responses and extrinsic variability due to context-specific factors of the environment, such as spatial heterogeneity. Statistically significant variation in the features of the calcium transients evoked by scratch wounding according to proximity to the wound edge was identified. The manifestation of distinct sub-populations of cells is considered central to the coordination of population-level response resulting in wound closure. The Royal Society 2015-04-06 /pmc/articles/PMC4387530/ /pubmed/25694543 http://dx.doi.org/10.1098/rsif.2014.1403 Text en http://creativecommons.org/licenses/by/4.0/ © 2015 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Articles Appleby, Peter A. Shabir, Saqib Southgate, Jennifer Walker, Dawn Sources of variability in cytosolic calcium transients triggered by stimulation of homogeneous uro-epithelial cell monolayers |
title | Sources of variability in cytosolic calcium transients triggered by stimulation of homogeneous uro-epithelial cell monolayers |
title_full | Sources of variability in cytosolic calcium transients triggered by stimulation of homogeneous uro-epithelial cell monolayers |
title_fullStr | Sources of variability in cytosolic calcium transients triggered by stimulation of homogeneous uro-epithelial cell monolayers |
title_full_unstemmed | Sources of variability in cytosolic calcium transients triggered by stimulation of homogeneous uro-epithelial cell monolayers |
title_short | Sources of variability in cytosolic calcium transients triggered by stimulation of homogeneous uro-epithelial cell monolayers |
title_sort | sources of variability in cytosolic calcium transients triggered by stimulation of homogeneous uro-epithelial cell monolayers |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387530/ https://www.ncbi.nlm.nih.gov/pubmed/25694543 http://dx.doi.org/10.1098/rsif.2014.1403 |
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