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Human fetal skin derived merkel cells display distinctive characteristics in vitro and in bio-engineered skin substitutes in vivo
Human skin contains specialized neuroendocrine Merkel cells responsible for fine touch sensation. In the present study, we performed in-depth analysis of Merkel cells in human fetal back skin. We revealed that these Merkel cells expressed cytokeratin 20 (CK20), were positive for the neuroendocrine m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520781/ https://www.ncbi.nlm.nih.gov/pubmed/36185452 http://dx.doi.org/10.3389/fbioe.2022.983870 |
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author | Michalak-Micka, Katarzyna Rütsche, Dominic Mazzone, Luca Büchler, Vanessa L. Moehrlen, Ueli Klar, Agnes S. Biedermann, Thomas |
author_facet | Michalak-Micka, Katarzyna Rütsche, Dominic Mazzone, Luca Büchler, Vanessa L. Moehrlen, Ueli Klar, Agnes S. Biedermann, Thomas |
author_sort | Michalak-Micka, Katarzyna |
collection | PubMed |
description | Human skin contains specialized neuroendocrine Merkel cells responsible for fine touch sensation. In the present study, we performed in-depth analysis of Merkel cells in human fetal back skin. We revealed that these Merkel cells expressed cytokeratin 20 (CK20), were positive for the neuroendocrine markers synaptophysin and chromogranin A, and the mechanosensitive ion channel Piezo2. Further, we demonstrated that Merkel cells were present in freshly isolated human fetal epidermal cells in vitro, and in tissue-engineered human dermo-epidermal skin substitutes 4 weeks after transplantation on immune-compromised rats. Merkel cells retained the expression of CK20, synaptophysin, chromogranin A, and Piezo2 after isolation and in culture, and in the skin substitutes after transplantation. Interestingly, we observed that in fetal skin and in skin substitutes, only Merkel cells were positive for CK8, while in culture, also non-Merkel cells showed positivity for CK8. In summary, human fetal Merkel cells showed phenotypical features confirming their cell identity. This findings are of pivotal importance for the future application of fetal tissue-engineered skin in clinics. |
format | Online Article Text |
id | pubmed-9520781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95207812022-09-30 Human fetal skin derived merkel cells display distinctive characteristics in vitro and in bio-engineered skin substitutes in vivo Michalak-Micka, Katarzyna Rütsche, Dominic Mazzone, Luca Büchler, Vanessa L. Moehrlen, Ueli Klar, Agnes S. Biedermann, Thomas Front Bioeng Biotechnol Bioengineering and Biotechnology Human skin contains specialized neuroendocrine Merkel cells responsible for fine touch sensation. In the present study, we performed in-depth analysis of Merkel cells in human fetal back skin. We revealed that these Merkel cells expressed cytokeratin 20 (CK20), were positive for the neuroendocrine markers synaptophysin and chromogranin A, and the mechanosensitive ion channel Piezo2. Further, we demonstrated that Merkel cells were present in freshly isolated human fetal epidermal cells in vitro, and in tissue-engineered human dermo-epidermal skin substitutes 4 weeks after transplantation on immune-compromised rats. Merkel cells retained the expression of CK20, synaptophysin, chromogranin A, and Piezo2 after isolation and in culture, and in the skin substitutes after transplantation. Interestingly, we observed that in fetal skin and in skin substitutes, only Merkel cells were positive for CK8, while in culture, also non-Merkel cells showed positivity for CK8. In summary, human fetal Merkel cells showed phenotypical features confirming their cell identity. This findings are of pivotal importance for the future application of fetal tissue-engineered skin in clinics. Frontiers Media S.A. 2022-09-15 /pmc/articles/PMC9520781/ /pubmed/36185452 http://dx.doi.org/10.3389/fbioe.2022.983870 Text en Copyright © 2022 Michalak-Micka, Rütsche, Mazzone, Büchler, Moehrlen, Klar and Biedermann. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Michalak-Micka, Katarzyna Rütsche, Dominic Mazzone, Luca Büchler, Vanessa L. Moehrlen, Ueli Klar, Agnes S. Biedermann, Thomas Human fetal skin derived merkel cells display distinctive characteristics in vitro and in bio-engineered skin substitutes in vivo |
title | Human fetal skin derived merkel cells display distinctive characteristics in vitro and in bio-engineered skin substitutes in vivo
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title_full | Human fetal skin derived merkel cells display distinctive characteristics in vitro and in bio-engineered skin substitutes in vivo
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title_fullStr | Human fetal skin derived merkel cells display distinctive characteristics in vitro and in bio-engineered skin substitutes in vivo
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title_full_unstemmed | Human fetal skin derived merkel cells display distinctive characteristics in vitro and in bio-engineered skin substitutes in vivo
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title_short | Human fetal skin derived merkel cells display distinctive characteristics in vitro and in bio-engineered skin substitutes in vivo
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title_sort | human fetal skin derived merkel cells display distinctive characteristics in vitro and in bio-engineered skin substitutes in vivo |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520781/ https://www.ncbi.nlm.nih.gov/pubmed/36185452 http://dx.doi.org/10.3389/fbioe.2022.983870 |
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