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Effect of Retinoic Acid in a Mouse Model of Allergic Rhinitis

PURPOSE: All-trans retinoic acid (ATRA) modulates immune responses by affecting T cells. Several studies have revealed that allergic inflammation of the lower airways is negatively associated with the vitamin A concentration. However, the role of ATRA in allergic inflammation of the upper airways is...

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Autores principales: Son, Hye-Lim, Park, Hyang-Rim, Park, Yong-Jin, Kim, Soo-Whan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605932/
https://www.ncbi.nlm.nih.gov/pubmed/26333706
http://dx.doi.org/10.4168/aair.2015.7.6.590
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author Son, Hye-Lim
Park, Hyang-Rim
Park, Yong-Jin
Kim, Soo-Whan
author_facet Son, Hye-Lim
Park, Hyang-Rim
Park, Yong-Jin
Kim, Soo-Whan
author_sort Son, Hye-Lim
collection PubMed
description PURPOSE: All-trans retinoic acid (ATRA) modulates immune responses by affecting T cells. Several studies have revealed that allergic inflammation of the lower airways is negatively associated with the vitamin A concentration. However, the role of ATRA in allergic inflammation of the upper airways is unclear. We investigated the effects of ATRA in an allergic rhinitis mouse model. METHODS: BALB/c mice except control groups (CON group) were sensitized with and challenged intra-nasally with Dermatophagoides farina (AR group). The ATRA groups were administered ATRA intraperitoneally. The steroid groups were administered steroid intranasally (ST group). Allergic symptoms and the average eosinophil number were counted. Cytokines and transcription factors were measured by Real-Time PCR and Western blotting. Der f-specific immunoglobulin E (IgE) was measured. Flow cytometry results of CD4(+)CD25(+)Foxp3(+) T cells were analyzed. RESULTS: The symptom scores were lower in the ATRA group than in the AR group and higher than in the CON group. The levels of IgE were lower in the ATRA group than in the AR group and higher than in the CON and ST groups. The levels of Foxp3, TGF-β, and IL-10 mRNA, as well as the percentage of CD4(+)CD25(+)Foxp3(+) T cells, were higher in the ATRA group than in theAR group. In the ATRA group the levels of IFN-γ mRNA were higher, and the levels of GATA-3 and IL-4 mRNA, and ROR-γt were lower. In Western blotting analyses, the expression patterns of all factors, except Foxp3, showed similar to those of mRNA expression. CONCLUSIONS: ATRA has anti-allergic effects in an allergic rhinitis model, and its underlying mechanisms mainly include the induction of regulatory T cells and the inhibition of Th2 responses.
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spelling pubmed-46059322015-11-01 Effect of Retinoic Acid in a Mouse Model of Allergic Rhinitis Son, Hye-Lim Park, Hyang-Rim Park, Yong-Jin Kim, Soo-Whan Allergy Asthma Immunol Res Original Article PURPOSE: All-trans retinoic acid (ATRA) modulates immune responses by affecting T cells. Several studies have revealed that allergic inflammation of the lower airways is negatively associated with the vitamin A concentration. However, the role of ATRA in allergic inflammation of the upper airways is unclear. We investigated the effects of ATRA in an allergic rhinitis mouse model. METHODS: BALB/c mice except control groups (CON group) were sensitized with and challenged intra-nasally with Dermatophagoides farina (AR group). The ATRA groups were administered ATRA intraperitoneally. The steroid groups were administered steroid intranasally (ST group). Allergic symptoms and the average eosinophil number were counted. Cytokines and transcription factors were measured by Real-Time PCR and Western blotting. Der f-specific immunoglobulin E (IgE) was measured. Flow cytometry results of CD4(+)CD25(+)Foxp3(+) T cells were analyzed. RESULTS: The symptom scores were lower in the ATRA group than in the AR group and higher than in the CON group. The levels of IgE were lower in the ATRA group than in the AR group and higher than in the CON and ST groups. The levels of Foxp3, TGF-β, and IL-10 mRNA, as well as the percentage of CD4(+)CD25(+)Foxp3(+) T cells, were higher in the ATRA group than in theAR group. In the ATRA group the levels of IFN-γ mRNA were higher, and the levels of GATA-3 and IL-4 mRNA, and ROR-γt were lower. In Western blotting analyses, the expression patterns of all factors, except Foxp3, showed similar to those of mRNA expression. CONCLUSIONS: ATRA has anti-allergic effects in an allergic rhinitis model, and its underlying mechanisms mainly include the induction of regulatory T cells and the inhibition of Th2 responses. The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2015-11 2015-06-02 /pmc/articles/PMC4605932/ /pubmed/26333706 http://dx.doi.org/10.4168/aair.2015.7.6.590 Text en Copyright © 2015 The Korean Academy of Asthma, Allergy and Clinical Immunology • The Korean Academy of Pediatric Allergy and Respiratory Disease http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Son, Hye-Lim
Park, Hyang-Rim
Park, Yong-Jin
Kim, Soo-Whan
Effect of Retinoic Acid in a Mouse Model of Allergic Rhinitis
title Effect of Retinoic Acid in a Mouse Model of Allergic Rhinitis
title_full Effect of Retinoic Acid in a Mouse Model of Allergic Rhinitis
title_fullStr Effect of Retinoic Acid in a Mouse Model of Allergic Rhinitis
title_full_unstemmed Effect of Retinoic Acid in a Mouse Model of Allergic Rhinitis
title_short Effect of Retinoic Acid in a Mouse Model of Allergic Rhinitis
title_sort effect of retinoic acid in a mouse model of allergic rhinitis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605932/
https://www.ncbi.nlm.nih.gov/pubmed/26333706
http://dx.doi.org/10.4168/aair.2015.7.6.590
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