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Epidermis-on-a-chip system to develop skin barrier and melanin mimicking model
In vitro skin models are rapidly developing and have been widely used in various fields as an alternative to traditional animal experiments. However, most traditional static skin models are constructed on Transwell plates without a dynamic three-dimensional (3D) culture microenvironment. Compared wi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126702/ https://www.ncbi.nlm.nih.gov/pubmed/37114033 http://dx.doi.org/10.1177/20417314231168529 |
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author | Li, Qiwei Wang, Chunyan Li, Xiaoran Zhang, Jing Zhang, Zilin Yang, Keyu Ouyang, Jun Zha, Shaohui Sha, Lifeng Ge, Jianjun Chen, Zaozao Gu, Zhongze |
author_facet | Li, Qiwei Wang, Chunyan Li, Xiaoran Zhang, Jing Zhang, Zilin Yang, Keyu Ouyang, Jun Zha, Shaohui Sha, Lifeng Ge, Jianjun Chen, Zaozao Gu, Zhongze |
author_sort | Li, Qiwei |
collection | PubMed |
description | In vitro skin models are rapidly developing and have been widely used in various fields as an alternative to traditional animal experiments. However, most traditional static skin models are constructed on Transwell plates without a dynamic three-dimensional (3D) culture microenvironment. Compared with native human and animal skin, such in vitro skin models are not completely biomimetic, especially regarding their thickness and permeability. Therefore, there is an urgent need to develop an automated biomimetic human microphysiological system (MPS), which can be used to construct in vitro skin models and improve bionic performance. In this work, we describe the development of a triple-well microfluidic-based epidermis-on-a-chip (EoC) system, possessing epidermis barrier and melanin-mimicking functions, as well as being semi-solid specimen friendly. The special design of our EoC system allows pasty and semi-solid substances to be effectively utilized in testing, as well as allowing for long-term culturing and imaging. The epidermis in this EoC system is well-differentiated, including basal, spinous, granular, and cornified layers with appropriate epidermis marker (e.g. keratin-10, keratin-14, involucrin, loricrin, and filaggrin) expression levels in corresponding layers. We further demonstrate that this organotypic chip can prevent permeation of over 99.83% of cascade blue (a 607 Da fluorescent molecule), and prednisone acetate (PA) was applied to test percutaneous penetration in the EoC. Finally, we tested the whitening effect of a cosmetic on the proposed EoC, thus demonstrating its efficacy. In summary, we developed a biomimetic EoC system for epidermis recreation, which could potentially serve as a useful tool for skin irritation, permeability, cosmetic evaluation, and drug safety tests. |
format | Online Article Text |
id | pubmed-10126702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-101267022023-04-26 Epidermis-on-a-chip system to develop skin barrier and melanin mimicking model Li, Qiwei Wang, Chunyan Li, Xiaoran Zhang, Jing Zhang, Zilin Yang, Keyu Ouyang, Jun Zha, Shaohui Sha, Lifeng Ge, Jianjun Chen, Zaozao Gu, Zhongze J Tissue Eng Original Article In vitro skin models are rapidly developing and have been widely used in various fields as an alternative to traditional animal experiments. However, most traditional static skin models are constructed on Transwell plates without a dynamic three-dimensional (3D) culture microenvironment. Compared with native human and animal skin, such in vitro skin models are not completely biomimetic, especially regarding their thickness and permeability. Therefore, there is an urgent need to develop an automated biomimetic human microphysiological system (MPS), which can be used to construct in vitro skin models and improve bionic performance. In this work, we describe the development of a triple-well microfluidic-based epidermis-on-a-chip (EoC) system, possessing epidermis barrier and melanin-mimicking functions, as well as being semi-solid specimen friendly. The special design of our EoC system allows pasty and semi-solid substances to be effectively utilized in testing, as well as allowing for long-term culturing and imaging. The epidermis in this EoC system is well-differentiated, including basal, spinous, granular, and cornified layers with appropriate epidermis marker (e.g. keratin-10, keratin-14, involucrin, loricrin, and filaggrin) expression levels in corresponding layers. We further demonstrate that this organotypic chip can prevent permeation of over 99.83% of cascade blue (a 607 Da fluorescent molecule), and prednisone acetate (PA) was applied to test percutaneous penetration in the EoC. Finally, we tested the whitening effect of a cosmetic on the proposed EoC, thus demonstrating its efficacy. In summary, we developed a biomimetic EoC system for epidermis recreation, which could potentially serve as a useful tool for skin irritation, permeability, cosmetic evaluation, and drug safety tests. SAGE Publications 2023-04-21 /pmc/articles/PMC10126702/ /pubmed/37114033 http://dx.doi.org/10.1177/20417314231168529 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Li, Qiwei Wang, Chunyan Li, Xiaoran Zhang, Jing Zhang, Zilin Yang, Keyu Ouyang, Jun Zha, Shaohui Sha, Lifeng Ge, Jianjun Chen, Zaozao Gu, Zhongze Epidermis-on-a-chip system to develop skin barrier and melanin mimicking model |
title | Epidermis-on-a-chip system to develop skin barrier and melanin mimicking model |
title_full | Epidermis-on-a-chip system to develop skin barrier and melanin mimicking model |
title_fullStr | Epidermis-on-a-chip system to develop skin barrier and melanin mimicking model |
title_full_unstemmed | Epidermis-on-a-chip system to develop skin barrier and melanin mimicking model |
title_short | Epidermis-on-a-chip system to develop skin barrier and melanin mimicking model |
title_sort | epidermis-on-a-chip system to develop skin barrier and melanin mimicking model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126702/ https://www.ncbi.nlm.nih.gov/pubmed/37114033 http://dx.doi.org/10.1177/20417314231168529 |
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