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Mathematical-model-guided development of full-thickness epidermal equivalent
Epidermal equivalents prepared with passaged keratinocytes are typically 10–20 μm thick, whereas intact human epidermis is up to 100 μm thick. Our established mathematical model of epidermal homeostasis predicted that the undulatory pattern of the papillary layer beneath the epidermis is a key deter...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6301960/ https://www.ncbi.nlm.nih.gov/pubmed/30573749 http://dx.doi.org/10.1038/s41598-018-36647-y |
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author | Kumamoto, Junichi Nakanishi, Shinobu Makita, Mio Uesaka, Masaaki Yasugahira, Yusuke Kobayashi, Yasuaki Nagayama, Masaharu Denda, Sumiko Denda, Mitsuhiro |
author_facet | Kumamoto, Junichi Nakanishi, Shinobu Makita, Mio Uesaka, Masaaki Yasugahira, Yusuke Kobayashi, Yasuaki Nagayama, Masaharu Denda, Sumiko Denda, Mitsuhiro |
author_sort | Kumamoto, Junichi |
collection | PubMed |
description | Epidermal equivalents prepared with passaged keratinocytes are typically 10–20 μm thick, whereas intact human epidermis is up to 100 μm thick. Our established mathematical model of epidermal homeostasis predicted that the undulatory pattern of the papillary layer beneath the epidermis is a key determinant of epidermal thickness. Here, we tested this prediction by seeding human keratinocytes on polyester textiles with various fiber-structural patterns in culture dishes exposed to air, aiming to develop a more physiologically realistic epidermal model using passaged keratinocytes. Textile substrate with fiber thickness and inter-fiber distance matching the computer predictions afforded a three-dimensional epidermal-equivalent model with thick stratum corneum and intercellular lamellar lipid structure. The basal layer structure was similar to that of human papillary layer. Cells located around the textile fibers were proliferating, as indicated by BrdU and YAP (Yes-associated protein) staining and expression of melanoma-associated chondroitin sulfate proteoglycan. Filaggrin, loricrin, claudin 1 and ZO-1 were all appropriately expressed. Silencing of transcriptional coactivator YAP with siRNA disturbed construction of the three-dimensional structure. Measurement of trans-epidermal water loss (TEWL) indicated that the model has excellent barrier function. Our results support the idea that mathematical modeling of complex biological processes can have predictive ability and practical value. |
format | Online Article Text |
id | pubmed-6301960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63019602018-12-26 Mathematical-model-guided development of full-thickness epidermal equivalent Kumamoto, Junichi Nakanishi, Shinobu Makita, Mio Uesaka, Masaaki Yasugahira, Yusuke Kobayashi, Yasuaki Nagayama, Masaharu Denda, Sumiko Denda, Mitsuhiro Sci Rep Article Epidermal equivalents prepared with passaged keratinocytes are typically 10–20 μm thick, whereas intact human epidermis is up to 100 μm thick. Our established mathematical model of epidermal homeostasis predicted that the undulatory pattern of the papillary layer beneath the epidermis is a key determinant of epidermal thickness. Here, we tested this prediction by seeding human keratinocytes on polyester textiles with various fiber-structural patterns in culture dishes exposed to air, aiming to develop a more physiologically realistic epidermal model using passaged keratinocytes. Textile substrate with fiber thickness and inter-fiber distance matching the computer predictions afforded a three-dimensional epidermal-equivalent model with thick stratum corneum and intercellular lamellar lipid structure. The basal layer structure was similar to that of human papillary layer. Cells located around the textile fibers were proliferating, as indicated by BrdU and YAP (Yes-associated protein) staining and expression of melanoma-associated chondroitin sulfate proteoglycan. Filaggrin, loricrin, claudin 1 and ZO-1 were all appropriately expressed. Silencing of transcriptional coactivator YAP with siRNA disturbed construction of the three-dimensional structure. Measurement of trans-epidermal water loss (TEWL) indicated that the model has excellent barrier function. Our results support the idea that mathematical modeling of complex biological processes can have predictive ability and practical value. Nature Publishing Group UK 2018-12-20 /pmc/articles/PMC6301960/ /pubmed/30573749 http://dx.doi.org/10.1038/s41598-018-36647-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kumamoto, Junichi Nakanishi, Shinobu Makita, Mio Uesaka, Masaaki Yasugahira, Yusuke Kobayashi, Yasuaki Nagayama, Masaharu Denda, Sumiko Denda, Mitsuhiro Mathematical-model-guided development of full-thickness epidermal equivalent |
title | Mathematical-model-guided development of full-thickness epidermal equivalent |
title_full | Mathematical-model-guided development of full-thickness epidermal equivalent |
title_fullStr | Mathematical-model-guided development of full-thickness epidermal equivalent |
title_full_unstemmed | Mathematical-model-guided development of full-thickness epidermal equivalent |
title_short | Mathematical-model-guided development of full-thickness epidermal equivalent |
title_sort | mathematical-model-guided development of full-thickness epidermal equivalent |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6301960/ https://www.ncbi.nlm.nih.gov/pubmed/30573749 http://dx.doi.org/10.1038/s41598-018-36647-y |
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