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Innate Type 2 Response to Aspergillus fumigatus in a Murine Model of Atopic Dermatitis–like Skin Inflammation

BACKGROUND: Atopic dermatitis (AD) is a chronic and relapsing inflammatory skin disease mediated by T helper type 2 (Th2) cells in acute phase. Group 2 innate lymphoid cells (ILCs) play a role in the initiation of the Th2 response. Although mold exposure is associated with the development of AD, stu...

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Autores principales: Park, Arum, Lee, Eun, Park, Hyojung, Park, Mee-Na, Lee, Jiho, Song, Kun Baek, Yoon, Jisun, Jung, Sungsu, Suh, Nayoung, Yoon, Jin, Yu, Jinho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524237/
https://www.ncbi.nlm.nih.gov/pubmed/34664800
http://dx.doi.org/10.3346/jkms.2021.36.e261
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author Park, Arum
Lee, Eun
Park, Hyojung
Park, Mee-Na
Lee, Jiho
Song, Kun Baek
Yoon, Jisun
Jung, Sungsu
Suh, Nayoung
Yoon, Jin
Yu, Jinho
author_facet Park, Arum
Lee, Eun
Park, Hyojung
Park, Mee-Na
Lee, Jiho
Song, Kun Baek
Yoon, Jisun
Jung, Sungsu
Suh, Nayoung
Yoon, Jin
Yu, Jinho
author_sort Park, Arum
collection PubMed
description BACKGROUND: Atopic dermatitis (AD) is a chronic and relapsing inflammatory skin disease mediated by T helper type 2 (Th2) cells in acute phase. Group 2 innate lymphoid cells (ILCs) play a role in the initiation of the Th2 response. Although mold exposure is associated with the development of AD, studies on the underlying mechanisms are lacking. This study investigated whether group 2 ILCs are involved in inflammation in AD-like skin induced by Aspergillus fumigatus (Af). METHODS: We investigated changes of group 2 ILCs population in Af-induced AD-like skin lesions. To induce AD-like skin lesions, Af extracts were applied to the dorsal skin of BALB/c and Rag1(−/−) mice five times per week, with repeat exposures at 2-week intervals. RESULTS: The clinical parameters were higher in the Af-treated group than in the control group. Histologic findings revealed epiderrmal and dermal thickening as well as eosinophil and mast cell infiltration into the skin of Af-treated mice. Populations of group 2 ILCs in the skin were also significantly higher in the Af-treated group. In addition, interleukin-33 mRNA expression was significantly higher in the skin lesions of the Af-treated mice. In the Rag1(−/−) mice lacking mature lymphocytes, AD-like skin lesions were still induced by Af and ILCs depletion using an anti-CD90.2 mAb lowered the Af-induced inflammatory response. CONCLUSIONS: Group 2 ILCs may play a role in a murine model of Af-induced AD-like skin lesions.
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spelling pubmed-85242372021-10-29 Innate Type 2 Response to Aspergillus fumigatus in a Murine Model of Atopic Dermatitis–like Skin Inflammation Park, Arum Lee, Eun Park, Hyojung Park, Mee-Na Lee, Jiho Song, Kun Baek Yoon, Jisun Jung, Sungsu Suh, Nayoung Yoon, Jin Yu, Jinho J Korean Med Sci Original Article BACKGROUND: Atopic dermatitis (AD) is a chronic and relapsing inflammatory skin disease mediated by T helper type 2 (Th2) cells in acute phase. Group 2 innate lymphoid cells (ILCs) play a role in the initiation of the Th2 response. Although mold exposure is associated with the development of AD, studies on the underlying mechanisms are lacking. This study investigated whether group 2 ILCs are involved in inflammation in AD-like skin induced by Aspergillus fumigatus (Af). METHODS: We investigated changes of group 2 ILCs population in Af-induced AD-like skin lesions. To induce AD-like skin lesions, Af extracts were applied to the dorsal skin of BALB/c and Rag1(−/−) mice five times per week, with repeat exposures at 2-week intervals. RESULTS: The clinical parameters were higher in the Af-treated group than in the control group. Histologic findings revealed epiderrmal and dermal thickening as well as eosinophil and mast cell infiltration into the skin of Af-treated mice. Populations of group 2 ILCs in the skin were also significantly higher in the Af-treated group. In addition, interleukin-33 mRNA expression was significantly higher in the skin lesions of the Af-treated mice. In the Rag1(−/−) mice lacking mature lymphocytes, AD-like skin lesions were still induced by Af and ILCs depletion using an anti-CD90.2 mAb lowered the Af-induced inflammatory response. CONCLUSIONS: Group 2 ILCs may play a role in a murine model of Af-induced AD-like skin lesions. The Korean Academy of Medical Sciences 2021-09-02 /pmc/articles/PMC8524237/ /pubmed/34664800 http://dx.doi.org/10.3346/jkms.2021.36.e261 Text en © 2021 The Korean Academy of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Park, Arum
Lee, Eun
Park, Hyojung
Park, Mee-Na
Lee, Jiho
Song, Kun Baek
Yoon, Jisun
Jung, Sungsu
Suh, Nayoung
Yoon, Jin
Yu, Jinho
Innate Type 2 Response to Aspergillus fumigatus in a Murine Model of Atopic Dermatitis–like Skin Inflammation
title Innate Type 2 Response to Aspergillus fumigatus in a Murine Model of Atopic Dermatitis–like Skin Inflammation
title_full Innate Type 2 Response to Aspergillus fumigatus in a Murine Model of Atopic Dermatitis–like Skin Inflammation
title_fullStr Innate Type 2 Response to Aspergillus fumigatus in a Murine Model of Atopic Dermatitis–like Skin Inflammation
title_full_unstemmed Innate Type 2 Response to Aspergillus fumigatus in a Murine Model of Atopic Dermatitis–like Skin Inflammation
title_short Innate Type 2 Response to Aspergillus fumigatus in a Murine Model of Atopic Dermatitis–like Skin Inflammation
title_sort innate type 2 response to aspergillus fumigatus in a murine model of atopic dermatitis–like skin inflammation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524237/
https://www.ncbi.nlm.nih.gov/pubmed/34664800
http://dx.doi.org/10.3346/jkms.2021.36.e261
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