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Identification of Merkel cells associated with neurons in engineered skin substitutes after grafting to full thickness wounds

Engineered skin substitutes (ESS), prepared using primary human fibroblasts and keratinocytes with a biopolymer scaffold, were shown to provide stable closure of excised burns, but relatively little is known about innervation of ESS after grafting. This study investigated innervation of ESS and, spe...

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Autores principales: Hahn, Jennifer M., Combs, Kelly A., Lloyd, Christopher M., McFarland, Kevin L., Boyce, Steven T., Supp, Dorothy M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400390/
https://www.ncbi.nlm.nih.gov/pubmed/30835771
http://dx.doi.org/10.1371/journal.pone.0213325
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author Hahn, Jennifer M.
Combs, Kelly A.
Lloyd, Christopher M.
McFarland, Kevin L.
Boyce, Steven T.
Supp, Dorothy M.
author_facet Hahn, Jennifer M.
Combs, Kelly A.
Lloyd, Christopher M.
McFarland, Kevin L.
Boyce, Steven T.
Supp, Dorothy M.
author_sort Hahn, Jennifer M.
collection PubMed
description Engineered skin substitutes (ESS), prepared using primary human fibroblasts and keratinocytes with a biopolymer scaffold, were shown to provide stable closure of excised burns, but relatively little is known about innervation of ESS after grafting. This study investigated innervation of ESS and, specifically, whether Merkel cells are present in healed grafts. Merkel cells are specialized neuroendocrine cells required for fine touch sensation in skin. We discovered cells positive for keratin 20 (KRT20), a general marker for Merkel cells, in the basal epidermis of ESS after transplantation to mice, suggesting the presence of Merkel cells. Cells expressing KRT20 were not observed in ESS in vitro. However, widely separated KRT20-positive cells were observed in basal epidermis of ESS by 2 weeks after grafting. By 4 weeks, these cells increased in number and expressed keratins 18 and 19, additional Merkel cells markers. Putative Merkel cell numbers increased further between weeks 6 and 14; their densities varied widely and no specific pattern of organization was observed, similar to Merkel cell localization in human skin. KRT20-positive cells co-expressed epidermal markers E-cadherin and keratin 15, suggesting derivation from the epidermal lineage, and neuroendocrine markers synaptophysin and chromogranin A, consistent with their identification as Merkel cells. By 4 weeks after grafting, some Merkel cells in engineered skin were associated with immature afferents expressing neurofilament-medium. By 8 weeks, Merkel cells were complexed with more mature neurons expressing neurofilament-heavy. Positive staining for human leukocyte antigen demonstrated that the Merkel cells in ESS were derived from grafted human cells. The results identify, for the first time, Merkel cell-neurite complexes in engineered skin in vivo. This suggests that fine touch sensation may be restored in ESS after grafting, although this must be confirmed with future functional studies.
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spelling pubmed-64003902019-03-17 Identification of Merkel cells associated with neurons in engineered skin substitutes after grafting to full thickness wounds Hahn, Jennifer M. Combs, Kelly A. Lloyd, Christopher M. McFarland, Kevin L. Boyce, Steven T. Supp, Dorothy M. PLoS One Research Article Engineered skin substitutes (ESS), prepared using primary human fibroblasts and keratinocytes with a biopolymer scaffold, were shown to provide stable closure of excised burns, but relatively little is known about innervation of ESS after grafting. This study investigated innervation of ESS and, specifically, whether Merkel cells are present in healed grafts. Merkel cells are specialized neuroendocrine cells required for fine touch sensation in skin. We discovered cells positive for keratin 20 (KRT20), a general marker for Merkel cells, in the basal epidermis of ESS after transplantation to mice, suggesting the presence of Merkel cells. Cells expressing KRT20 were not observed in ESS in vitro. However, widely separated KRT20-positive cells were observed in basal epidermis of ESS by 2 weeks after grafting. By 4 weeks, these cells increased in number and expressed keratins 18 and 19, additional Merkel cells markers. Putative Merkel cell numbers increased further between weeks 6 and 14; their densities varied widely and no specific pattern of organization was observed, similar to Merkel cell localization in human skin. KRT20-positive cells co-expressed epidermal markers E-cadherin and keratin 15, suggesting derivation from the epidermal lineage, and neuroendocrine markers synaptophysin and chromogranin A, consistent with their identification as Merkel cells. By 4 weeks after grafting, some Merkel cells in engineered skin were associated with immature afferents expressing neurofilament-medium. By 8 weeks, Merkel cells were complexed with more mature neurons expressing neurofilament-heavy. Positive staining for human leukocyte antigen demonstrated that the Merkel cells in ESS were derived from grafted human cells. The results identify, for the first time, Merkel cell-neurite complexes in engineered skin in vivo. This suggests that fine touch sensation may be restored in ESS after grafting, although this must be confirmed with future functional studies. Public Library of Science 2019-03-05 /pmc/articles/PMC6400390/ /pubmed/30835771 http://dx.doi.org/10.1371/journal.pone.0213325 Text en © 2019 Hahn 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
Hahn, Jennifer M.
Combs, Kelly A.
Lloyd, Christopher M.
McFarland, Kevin L.
Boyce, Steven T.
Supp, Dorothy M.
Identification of Merkel cells associated with neurons in engineered skin substitutes after grafting to full thickness wounds
title Identification of Merkel cells associated with neurons in engineered skin substitutes after grafting to full thickness wounds
title_full Identification of Merkel cells associated with neurons in engineered skin substitutes after grafting to full thickness wounds
title_fullStr Identification of Merkel cells associated with neurons in engineered skin substitutes after grafting to full thickness wounds
title_full_unstemmed Identification of Merkel cells associated with neurons in engineered skin substitutes after grafting to full thickness wounds
title_short Identification of Merkel cells associated with neurons in engineered skin substitutes after grafting to full thickness wounds
title_sort identification of merkel cells associated with neurons in engineered skin substitutes after grafting to full thickness wounds
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400390/
https://www.ncbi.nlm.nih.gov/pubmed/30835771
http://dx.doi.org/10.1371/journal.pone.0213325
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