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Perlecan expression influences the keratin 15‐positive cell population fate in the epidermis of aging skin

The epidermis is continuously renewed by stem cell proliferation and differentiation. Basal keratinocytes append the dermal‐epidermal junction, a cell surface‐associated, extracellular matrix that provides structural support and influences their behaviour. It consists of laminins, type IV collagen,...

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Autores principales: Dos Santos, Morgan, Michopoulou, Anna, André‐Frei, Valérie, Boulesteix, Sophie, Guicher, Christine, Dayan, Guila, Whitelock, John, Damour, Odile, Rousselle, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4925826/
https://www.ncbi.nlm.nih.gov/pubmed/26996820
http://dx.doi.org/10.18632/aging.100928
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author Dos Santos, Morgan
Michopoulou, Anna
André‐Frei, Valérie
Boulesteix, Sophie
Guicher, Christine
Dayan, Guila
Whitelock, John
Damour, Odile
Rousselle, Patricia
author_facet Dos Santos, Morgan
Michopoulou, Anna
André‐Frei, Valérie
Boulesteix, Sophie
Guicher, Christine
Dayan, Guila
Whitelock, John
Damour, Odile
Rousselle, Patricia
author_sort Dos Santos, Morgan
collection PubMed
description The epidermis is continuously renewed by stem cell proliferation and differentiation. Basal keratinocytes append the dermal‐epidermal junction, a cell surface‐associated, extracellular matrix that provides structural support and influences their behaviour. It consists of laminins, type IV collagen, nidogens, and perlecan, which are necessary for tissue organization and structural integrity. Perlecan is a heparan sulfate proteoglycan known to be involved in keratinocyte survival and differentiation. Aging affects the dermal epidermal junction resulting in decreased contact with keratinocytes, thus impacting epidermal renewal and homeostasis. We found that perlecan expression decreased during chronological skin aging. Our in vitro studies revealed reduced perlecan transcript levels in aged keratinocytes. The production of in vitro skin models revealed that aged keratinocytes formed a thin and poorly organized epidermis. Supplementing these models with purified perlecan reversed the phenomenon allowing restoration of a well‐differentiated multi‐layered epithelium. Perlecan down‐regulation in cultured keratinocytes caused depletion of the cell population that expressed keratin 15. This phenomenon depended on the perlecan heparan sulphate moieties, which suggested the involvement of a growth factor. Finally, we found defects in keratin 15 expression in the epidermis of aging skin. This study highlighted a new role for perlecan in maintaining the self‐renewal capacity of basal keratinocytes.
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spelling pubmed-49258262016-07-01 Perlecan expression influences the keratin 15‐positive cell population fate in the epidermis of aging skin Dos Santos, Morgan Michopoulou, Anna André‐Frei, Valérie Boulesteix, Sophie Guicher, Christine Dayan, Guila Whitelock, John Damour, Odile Rousselle, Patricia Aging (Albany NY) Research Paper The epidermis is continuously renewed by stem cell proliferation and differentiation. Basal keratinocytes append the dermal‐epidermal junction, a cell surface‐associated, extracellular matrix that provides structural support and influences their behaviour. It consists of laminins, type IV collagen, nidogens, and perlecan, which are necessary for tissue organization and structural integrity. Perlecan is a heparan sulfate proteoglycan known to be involved in keratinocyte survival and differentiation. Aging affects the dermal epidermal junction resulting in decreased contact with keratinocytes, thus impacting epidermal renewal and homeostasis. We found that perlecan expression decreased during chronological skin aging. Our in vitro studies revealed reduced perlecan transcript levels in aged keratinocytes. The production of in vitro skin models revealed that aged keratinocytes formed a thin and poorly organized epidermis. Supplementing these models with purified perlecan reversed the phenomenon allowing restoration of a well‐differentiated multi‐layered epithelium. Perlecan down‐regulation in cultured keratinocytes caused depletion of the cell population that expressed keratin 15. This phenomenon depended on the perlecan heparan sulphate moieties, which suggested the involvement of a growth factor. Finally, we found defects in keratin 15 expression in the epidermis of aging skin. This study highlighted a new role for perlecan in maintaining the self‐renewal capacity of basal keratinocytes. Impact Journals LLC 2016-03-17 /pmc/articles/PMC4925826/ /pubmed/26996820 http://dx.doi.org/10.18632/aging.100928 Text en Copyright: © 2016 Dos Santos et al. http://creativecommons.org/licenses/by/2.5/ 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 credited.
spellingShingle Research Paper
Dos Santos, Morgan
Michopoulou, Anna
André‐Frei, Valérie
Boulesteix, Sophie
Guicher, Christine
Dayan, Guila
Whitelock, John
Damour, Odile
Rousselle, Patricia
Perlecan expression influences the keratin 15‐positive cell population fate in the epidermis of aging skin
title Perlecan expression influences the keratin 15‐positive cell population fate in the epidermis of aging skin
title_full Perlecan expression influences the keratin 15‐positive cell population fate in the epidermis of aging skin
title_fullStr Perlecan expression influences the keratin 15‐positive cell population fate in the epidermis of aging skin
title_full_unstemmed Perlecan expression influences the keratin 15‐positive cell population fate in the epidermis of aging skin
title_short Perlecan expression influences the keratin 15‐positive cell population fate in the epidermis of aging skin
title_sort perlecan expression influences the keratin 15‐positive cell population fate in the epidermis of aging skin
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4925826/
https://www.ncbi.nlm.nih.gov/pubmed/26996820
http://dx.doi.org/10.18632/aging.100928
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