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Skin-on-a-chip model simulating inflammation, edema and drug-based treatment
Recent advances in microfluidic cell cultures enable the construction of in vitro human skin models that can be used for drug toxicity testing, disease study. However, current in vitro skin model have limitations to emulate real human skin due to the simplicity of model. In this paper, we describe t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116589/ https://www.ncbi.nlm.nih.gov/pubmed/27869150 http://dx.doi.org/10.1038/srep37471 |
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author | Wufuer, Maierdanjiang Lee, GeonHui Hur, Woojune Jeon, Byoungjun Kim, Byung Jun Choi, Tae Hyun Lee, SangHoon |
author_facet | Wufuer, Maierdanjiang Lee, GeonHui Hur, Woojune Jeon, Byoungjun Kim, Byung Jun Choi, Tae Hyun Lee, SangHoon |
author_sort | Wufuer, Maierdanjiang |
collection | PubMed |
description | Recent advances in microfluidic cell cultures enable the construction of in vitro human skin models that can be used for drug toxicity testing, disease study. However, current in vitro skin model have limitations to emulate real human skin due to the simplicity of model. In this paper, we describe the development of ‘skin-on-a-chip’ to mimic the structures and functional responses of the human skin. The proposed model consists of 3 layers, on which epidermal, dermal and endothelial components originated from human, were cultured. The microfluidic device was designed for co-culture of human skin cells and each layer was separated by using porous membranes to allow interlayer communication. Skin inflammation and edema were induced by applying tumor necrosis factor alpha on dermal layer to demonstrate the functionality of the system. The expression levels of proinflammatory cytokines were analyzed to illustrate the feasibility. In addition, we evaluated the efficacy of therapeutic drug testing model using our skin chip. The function of skin barrier was evaluated by staining tight junctions and measuring a permeability of endothelium. Our results suggest that the skin-on-a-chip model can potentially be used for constructing in vitro skin disease models or for testing the toxicity of cosmetics or drugs. |
format | Online Article Text |
id | pubmed-5116589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51165892016-11-28 Skin-on-a-chip model simulating inflammation, edema and drug-based treatment Wufuer, Maierdanjiang Lee, GeonHui Hur, Woojune Jeon, Byoungjun Kim, Byung Jun Choi, Tae Hyun Lee, SangHoon Sci Rep Article Recent advances in microfluidic cell cultures enable the construction of in vitro human skin models that can be used for drug toxicity testing, disease study. However, current in vitro skin model have limitations to emulate real human skin due to the simplicity of model. In this paper, we describe the development of ‘skin-on-a-chip’ to mimic the structures and functional responses of the human skin. The proposed model consists of 3 layers, on which epidermal, dermal and endothelial components originated from human, were cultured. The microfluidic device was designed for co-culture of human skin cells and each layer was separated by using porous membranes to allow interlayer communication. Skin inflammation and edema were induced by applying tumor necrosis factor alpha on dermal layer to demonstrate the functionality of the system. The expression levels of proinflammatory cytokines were analyzed to illustrate the feasibility. In addition, we evaluated the efficacy of therapeutic drug testing model using our skin chip. The function of skin barrier was evaluated by staining tight junctions and measuring a permeability of endothelium. Our results suggest that the skin-on-a-chip model can potentially be used for constructing in vitro skin disease models or for testing the toxicity of cosmetics or drugs. Nature Publishing Group 2016-11-21 /pmc/articles/PMC5116589/ /pubmed/27869150 http://dx.doi.org/10.1038/srep37471 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wufuer, Maierdanjiang Lee, GeonHui Hur, Woojune Jeon, Byoungjun Kim, Byung Jun Choi, Tae Hyun Lee, SangHoon Skin-on-a-chip model simulating inflammation, edema and drug-based treatment |
title | Skin-on-a-chip model simulating inflammation, edema and drug-based treatment |
title_full | Skin-on-a-chip model simulating inflammation, edema and drug-based treatment |
title_fullStr | Skin-on-a-chip model simulating inflammation, edema and drug-based treatment |
title_full_unstemmed | Skin-on-a-chip model simulating inflammation, edema and drug-based treatment |
title_short | Skin-on-a-chip model simulating inflammation, edema and drug-based treatment |
title_sort | skin-on-a-chip model simulating inflammation, edema and drug-based treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116589/ https://www.ncbi.nlm.nih.gov/pubmed/27869150 http://dx.doi.org/10.1038/srep37471 |
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