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Towards a Quantitative Theory of Epidermal Calcium Profile Formation in Unwounded Skin

We propose and mathematically examine a theory of calcium profile formation in unwounded mammalian epidermis based on: changes in keratinocyte proliferation, fluid and calcium exchange with the extracellular fluid during these cells’ passage through the epidermal sublayers, and the barrier functions...

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Detalles Bibliográficos
Autores principales: Adams, Matthew P., Mallet, Daniel G., Pettet, Graeme J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4308082/
https://www.ncbi.nlm.nih.gov/pubmed/25625723
http://dx.doi.org/10.1371/journal.pone.0116751
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author Adams, Matthew P.
Mallet, Daniel G.
Pettet, Graeme J.
author_facet Adams, Matthew P.
Mallet, Daniel G.
Pettet, Graeme J.
author_sort Adams, Matthew P.
collection PubMed
description We propose and mathematically examine a theory of calcium profile formation in unwounded mammalian epidermis based on: changes in keratinocyte proliferation, fluid and calcium exchange with the extracellular fluid during these cells’ passage through the epidermal sublayers, and the barrier functions of both the stratum corneum and tight junctions localised in the stratum granulosum. Using this theory, we develop a mathematical model that predicts epidermal sublayer transit times, partitioning of the epidermal calcium gradient between intracellular and extracellular domains, and the permeability of the tight junction barrier to calcium ions. Comparison of our model’s predictions of epidermal transit times with experimental data indicates that keratinocytes lose at least 87% of their volume during their disintegration to become corneocytes. Intracellular calcium is suggested as the main contributor to the epidermal calcium gradient, with its distribution actively regulated by a phenotypic switch in calcium exchange between keratinocytes and extracellular fluid present at the boundary between the stratum spinosum and the stratum granulosum. Formation of the extracellular calcium distribution, which rises in concentration through the stratum granulosum towards the skin surface, is attributed to a tight junction barrier in this sublayer possessing permeability to calcium ions that is less than 15 nm s(−1) in human epidermis and less than 37 nm s(−1) in murine epidermis. Future experimental work may refine the presented theory and reduce the mathematical uncertainty present in the model predictions.
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spelling pubmed-43080822015-02-06 Towards a Quantitative Theory of Epidermal Calcium Profile Formation in Unwounded Skin Adams, Matthew P. Mallet, Daniel G. Pettet, Graeme J. PLoS One Research Article We propose and mathematically examine a theory of calcium profile formation in unwounded mammalian epidermis based on: changes in keratinocyte proliferation, fluid and calcium exchange with the extracellular fluid during these cells’ passage through the epidermal sublayers, and the barrier functions of both the stratum corneum and tight junctions localised in the stratum granulosum. Using this theory, we develop a mathematical model that predicts epidermal sublayer transit times, partitioning of the epidermal calcium gradient between intracellular and extracellular domains, and the permeability of the tight junction barrier to calcium ions. Comparison of our model’s predictions of epidermal transit times with experimental data indicates that keratinocytes lose at least 87% of their volume during their disintegration to become corneocytes. Intracellular calcium is suggested as the main contributor to the epidermal calcium gradient, with its distribution actively regulated by a phenotypic switch in calcium exchange between keratinocytes and extracellular fluid present at the boundary between the stratum spinosum and the stratum granulosum. Formation of the extracellular calcium distribution, which rises in concentration through the stratum granulosum towards the skin surface, is attributed to a tight junction barrier in this sublayer possessing permeability to calcium ions that is less than 15 nm s(−1) in human epidermis and less than 37 nm s(−1) in murine epidermis. Future experimental work may refine the presented theory and reduce the mathematical uncertainty present in the model predictions. Public Library of Science 2015-01-27 /pmc/articles/PMC4308082/ /pubmed/25625723 http://dx.doi.org/10.1371/journal.pone.0116751 Text en © 2015 Adams 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
Adams, Matthew P.
Mallet, Daniel G.
Pettet, Graeme J.
Towards a Quantitative Theory of Epidermal Calcium Profile Formation in Unwounded Skin
title Towards a Quantitative Theory of Epidermal Calcium Profile Formation in Unwounded Skin
title_full Towards a Quantitative Theory of Epidermal Calcium Profile Formation in Unwounded Skin
title_fullStr Towards a Quantitative Theory of Epidermal Calcium Profile Formation in Unwounded Skin
title_full_unstemmed Towards a Quantitative Theory of Epidermal Calcium Profile Formation in Unwounded Skin
title_short Towards a Quantitative Theory of Epidermal Calcium Profile Formation in Unwounded Skin
title_sort towards a quantitative theory of epidermal calcium profile formation in unwounded skin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4308082/
https://www.ncbi.nlm.nih.gov/pubmed/25625723
http://dx.doi.org/10.1371/journal.pone.0116751
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