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Gp130 Promotes Inflammation via the STAT3/JAK2 Pathway in Allergic Conjunctivitis

PURPOSE: Allergic conjunctivitis (AC) is a common allergic condition worldwide that requires accurate screening and early diagnosis. We found that gp130 is essential for AC, as gp130 levels are elevated in AC. Therefore, this study aimed to elucidate the functions and the possible underlying mechani...

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Autores principales: Bao, Jiayu, Zhang, Peng, Wu, Binge, Wang, Jingyi, Li, Siyuan, Li, Ao, Jie, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082384/
https://www.ncbi.nlm.nih.gov/pubmed/37022703
http://dx.doi.org/10.1167/iovs.64.4.5
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author Bao, Jiayu
Zhang, Peng
Wu, Binge
Wang, Jingyi
Li, Siyuan
Li, Ao
Jie, Ying
author_facet Bao, Jiayu
Zhang, Peng
Wu, Binge
Wang, Jingyi
Li, Siyuan
Li, Ao
Jie, Ying
author_sort Bao, Jiayu
collection PubMed
description PURPOSE: Allergic conjunctivitis (AC) is a common allergic condition worldwide that requires accurate screening and early diagnosis. We found that gp130 is essential for AC, as gp130 levels are elevated in AC. Therefore, this study aimed to elucidate the functions and the possible underlying mechanisms of gp130 in AC. METHODS: To compare mRNA expression profiles, the conjunctival tissues of BALB/c mice with ovalbumin (OVA)-induced AC were subjected to RNA-sequencing (RNA-seq) analysis followed by bioinformatic analysis. A nonrandomized study involving 57 patients with AC and 24 sex- and age-matched healthy individuals was conducted. A protein chip was used to detect cytokine levels in patient tears. Differentially expressed proteins in patient serum were detected using label-free quantitative mass spectrometry. Histamine-stimulated conjunctival epithelial cells (HConEpiCs) were used to construct a cell model. LMT-28 which can inhibit gp130 phosphorylation was dropped onto the murine ocular surface, and the resulting symptoms were observed. RESULTS: Gp130 is upregulated in the conjunctival tissues of OVA-induced mice, the serum and tears of patients, and the histamine-stimulated HConEpiCs. Signal transducer and activator of transcription 3 (STAT3) and Janus kinase 2 (JAK2) were upregulated in the conjunctival tissues of mice with OVA-induced AC and in HConEpiCs. Ocular surface inflammation was significantly relieved in LMT-28-treated mice. The expression of IgE, IL-4, IL-5, and IL-13 in serum of LMT-28-treated mice decreased. The number of mast cells in conjunctival tissue was decreased compared with OVA-induced mice. CONCLUSIONS: Gp130 may play an important role in AC via the gp130/JAK2/STAT3 pathway. Inhibiting gp130 phosphorylation alleviates ocular surface inflammation in mice, presenting a potential treatment approach for AC.
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spelling pubmed-100823842023-04-09 Gp130 Promotes Inflammation via the STAT3/JAK2 Pathway in Allergic Conjunctivitis Bao, Jiayu Zhang, Peng Wu, Binge Wang, Jingyi Li, Siyuan Li, Ao Jie, Ying Invest Ophthalmol Vis Sci Biochemistry and Molecular Biology PURPOSE: Allergic conjunctivitis (AC) is a common allergic condition worldwide that requires accurate screening and early diagnosis. We found that gp130 is essential for AC, as gp130 levels are elevated in AC. Therefore, this study aimed to elucidate the functions and the possible underlying mechanisms of gp130 in AC. METHODS: To compare mRNA expression profiles, the conjunctival tissues of BALB/c mice with ovalbumin (OVA)-induced AC were subjected to RNA-sequencing (RNA-seq) analysis followed by bioinformatic analysis. A nonrandomized study involving 57 patients with AC and 24 sex- and age-matched healthy individuals was conducted. A protein chip was used to detect cytokine levels in patient tears. Differentially expressed proteins in patient serum were detected using label-free quantitative mass spectrometry. Histamine-stimulated conjunctival epithelial cells (HConEpiCs) were used to construct a cell model. LMT-28 which can inhibit gp130 phosphorylation was dropped onto the murine ocular surface, and the resulting symptoms were observed. RESULTS: Gp130 is upregulated in the conjunctival tissues of OVA-induced mice, the serum and tears of patients, and the histamine-stimulated HConEpiCs. Signal transducer and activator of transcription 3 (STAT3) and Janus kinase 2 (JAK2) were upregulated in the conjunctival tissues of mice with OVA-induced AC and in HConEpiCs. Ocular surface inflammation was significantly relieved in LMT-28-treated mice. The expression of IgE, IL-4, IL-5, and IL-13 in serum of LMT-28-treated mice decreased. The number of mast cells in conjunctival tissue was decreased compared with OVA-induced mice. CONCLUSIONS: Gp130 may play an important role in AC via the gp130/JAK2/STAT3 pathway. Inhibiting gp130 phosphorylation alleviates ocular surface inflammation in mice, presenting a potential treatment approach for AC. The Association for Research in Vision and Ophthalmology 2023-04-06 /pmc/articles/PMC10082384/ /pubmed/37022703 http://dx.doi.org/10.1167/iovs.64.4.5 Text en Copyright 2023 The Authors https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License.
spellingShingle Biochemistry and Molecular Biology
Bao, Jiayu
Zhang, Peng
Wu, Binge
Wang, Jingyi
Li, Siyuan
Li, Ao
Jie, Ying
Gp130 Promotes Inflammation via the STAT3/JAK2 Pathway in Allergic Conjunctivitis
title Gp130 Promotes Inflammation via the STAT3/JAK2 Pathway in Allergic Conjunctivitis
title_full Gp130 Promotes Inflammation via the STAT3/JAK2 Pathway in Allergic Conjunctivitis
title_fullStr Gp130 Promotes Inflammation via the STAT3/JAK2 Pathway in Allergic Conjunctivitis
title_full_unstemmed Gp130 Promotes Inflammation via the STAT3/JAK2 Pathway in Allergic Conjunctivitis
title_short Gp130 Promotes Inflammation via the STAT3/JAK2 Pathway in Allergic Conjunctivitis
title_sort gp130 promotes inflammation via the stat3/jak2 pathway in allergic conjunctivitis
topic Biochemistry and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082384/
https://www.ncbi.nlm.nih.gov/pubmed/37022703
http://dx.doi.org/10.1167/iovs.64.4.5
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