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Anti-atopic dermatitis effect of fish collagen on house dust mite-induced mice and HaCaT keratinocytes

Collagen, a major structural protein in mammalian tissues, is effective against skin wounds and osteoarthritis. Although bovine and porcine collagens have mainly been used, several potential risks of mammalian collagen have led to the use of fish collagen (FC) as an alternative. FC and its peptides...

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Autores principales: Kim, Hye-Min, Jin, Bo-Ram, Lee, Jin-Sil, Jo, Eun Heui, Park, Min Cheol, An, Hyo-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10492863/
https://www.ncbi.nlm.nih.gov/pubmed/37689763
http://dx.doi.org/10.1038/s41598-023-41831-w
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author Kim, Hye-Min
Jin, Bo-Ram
Lee, Jin-Sil
Jo, Eun Heui
Park, Min Cheol
An, Hyo-Jin
author_facet Kim, Hye-Min
Jin, Bo-Ram
Lee, Jin-Sil
Jo, Eun Heui
Park, Min Cheol
An, Hyo-Jin
author_sort Kim, Hye-Min
collection PubMed
description Collagen, a major structural protein in mammalian tissues, is effective against skin wounds and osteoarthritis. Although bovine and porcine collagens have mainly been used, several potential risks of mammalian collagen have led to the use of fish collagen (FC) as an alternative. FC and its peptides are used as common cosmeceutical products because of their antihypertensive, anti-bacterial, and antioxidant activities. Despite the effects of FC on wrinkle reduction, UV-protection, and wound healing, the relationship between FC and atopic dermatitis (AD) has not yet been reported. Therefore, we investigated the anti-AD effects of FC against house dust mite (Dermatophagoides farinae, HDM)-induced AD in NC/Nga mice and TNF-α/IFN-γ-stimulated HaCaT keratinocytes. FC alleviated AD apparent symptoms, such as dermatitis score, transepidermal water loss, epidermal thickness, and mast cell infiltration upon declining pro-inflammatory cytokines and mediators, IL-6, IL-5, IL-13, TSLP, and TNF-α. The skin barrier protein, filaggrin, was also recovered by FC administration in vivo and in vitro. Immune response and skin barrier dysfunction are both mitigated by three routes of FC administration: oral, topical, and both routes via the regulation of IκB, MAPKs, and STATs pathways. In summary, FC could be a potential therapeutic agent for AD by regulating immune balance and skin barrier function.
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spelling pubmed-104928632023-09-11 Anti-atopic dermatitis effect of fish collagen on house dust mite-induced mice and HaCaT keratinocytes Kim, Hye-Min Jin, Bo-Ram Lee, Jin-Sil Jo, Eun Heui Park, Min Cheol An, Hyo-Jin Sci Rep Article Collagen, a major structural protein in mammalian tissues, is effective against skin wounds and osteoarthritis. Although bovine and porcine collagens have mainly been used, several potential risks of mammalian collagen have led to the use of fish collagen (FC) as an alternative. FC and its peptides are used as common cosmeceutical products because of their antihypertensive, anti-bacterial, and antioxidant activities. Despite the effects of FC on wrinkle reduction, UV-protection, and wound healing, the relationship between FC and atopic dermatitis (AD) has not yet been reported. Therefore, we investigated the anti-AD effects of FC against house dust mite (Dermatophagoides farinae, HDM)-induced AD in NC/Nga mice and TNF-α/IFN-γ-stimulated HaCaT keratinocytes. FC alleviated AD apparent symptoms, such as dermatitis score, transepidermal water loss, epidermal thickness, and mast cell infiltration upon declining pro-inflammatory cytokines and mediators, IL-6, IL-5, IL-13, TSLP, and TNF-α. The skin barrier protein, filaggrin, was also recovered by FC administration in vivo and in vitro. Immune response and skin barrier dysfunction are both mitigated by three routes of FC administration: oral, topical, and both routes via the regulation of IκB, MAPKs, and STATs pathways. In summary, FC could be a potential therapeutic agent for AD by regulating immune balance and skin barrier function. Nature Publishing Group UK 2023-09-09 /pmc/articles/PMC10492863/ /pubmed/37689763 http://dx.doi.org/10.1038/s41598-023-41831-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kim, Hye-Min
Jin, Bo-Ram
Lee, Jin-Sil
Jo, Eun Heui
Park, Min Cheol
An, Hyo-Jin
Anti-atopic dermatitis effect of fish collagen on house dust mite-induced mice and HaCaT keratinocytes
title Anti-atopic dermatitis effect of fish collagen on house dust mite-induced mice and HaCaT keratinocytes
title_full Anti-atopic dermatitis effect of fish collagen on house dust mite-induced mice and HaCaT keratinocytes
title_fullStr Anti-atopic dermatitis effect of fish collagen on house dust mite-induced mice and HaCaT keratinocytes
title_full_unstemmed Anti-atopic dermatitis effect of fish collagen on house dust mite-induced mice and HaCaT keratinocytes
title_short Anti-atopic dermatitis effect of fish collagen on house dust mite-induced mice and HaCaT keratinocytes
title_sort anti-atopic dermatitis effect of fish collagen on house dust mite-induced mice and hacat keratinocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10492863/
https://www.ncbi.nlm.nih.gov/pubmed/37689763
http://dx.doi.org/10.1038/s41598-023-41831-w
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