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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...

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Autores principales: Kumamoto, Junichi, Nakanishi, Shinobu, Makita, Mio, Uesaka, Masaaki, Yasugahira, Yusuke, Kobayashi, Yasuaki, Nagayama, Masaharu, Denda, Sumiko, Denda, Mitsuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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