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Protective role of IL-17-producing γδ T cells in a laser-induced choroidal neovascularization mouse model

BACKGROUND: Vision loss in patients with wet/exudative age-related macular degeneration (AMD) is associated with choroidal neovascularization (CNV), and AMD is the leading cause of irreversible vision impairment in older adults. Interleukin-17A (IL-17A) is a component of the microenvironment associa...

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Autores principales: Chang, Yu-Hsien, Hsing, Chung-Hsi, Chiu, Chiao-Juno, Wu, Yi-Rou, Hsu, Sheng-Min, Hsu, Yu-Hsiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676594/
https://www.ncbi.nlm.nih.gov/pubmed/38007487
http://dx.doi.org/10.1186/s12974-023-02952-1
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author Chang, Yu-Hsien
Hsing, Chung-Hsi
Chiu, Chiao-Juno
Wu, Yi-Rou
Hsu, Sheng-Min
Hsu, Yu-Hsiang
author_facet Chang, Yu-Hsien
Hsing, Chung-Hsi
Chiu, Chiao-Juno
Wu, Yi-Rou
Hsu, Sheng-Min
Hsu, Yu-Hsiang
author_sort Chang, Yu-Hsien
collection PubMed
description BACKGROUND: Vision loss in patients with wet/exudative age-related macular degeneration (AMD) is associated with choroidal neovascularization (CNV), and AMD is the leading cause of irreversible vision impairment in older adults. Interleukin-17A (IL-17A) is a component of the microenvironment associated with some autoimmune diseases. Previous studies have indicated that wet AMD patients have elevated serum IL-17A levels. However, the effect of IL-17A on AMD progression needs to be better understood. We aimed to investigate the role of IL-17A in a laser-induced CNV mouse model. METHODS: We established a laser-induced CNV mouse model in wild-type (WT) and IL-17A-deficient mice and then evaluated the disease severity of these mice by using fluorescence angiography. We performed enzyme-linked immunosorbent assay (ELISA) and fluorescence-activated cell sorting (FACS) to analyze the levels of IL-17A and to investigate the immune cell populations in the eyes of WT and IL-17A-deficient mice. We used ARPE-19 cells to clarify the effect of IL-17A under oxidative stress. RESULTS: In the laser-induced CNV model, the CNV lesions were larger in IL-17A-deficient mice than in WT mice. The numbers of γδ T cells, CD3(+)CD4(+)RORγt(+) T cells, Treg cells, and neutrophils were decreased and the number of macrophages was increased in the eyes of IL-17A-deficient mice compared with WT mice. In WT mice, IL-17A-producing γδ T-cell numbers increased in a time-dependent manner from day 7 to 28 after laser injury. IL-6 levels increased and IL-10, IL-24, IL-17F, and GM-CSF levels decreased in the eyes of IL-17A-deficient mice after laser injury. In vitro, IL-17A inhibited apoptosis and induced the expression of the antioxidant protein HO-1 in ARPE-19 cells under oxidative stress conditions. IL-17A facilitated the repair of oxidative stress-induced barrier dysfunction in ARPE-19 cells. CONCLUSIONS: Our findings provide new insight into the protective effect of IL-17A in a laser-induced CNV model and reveal a novel regulatory role of IL-17A-producing γδ T cells in the ocular microenvironment in wet AMD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-023-02952-1.
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spelling pubmed-106765942023-11-25 Protective role of IL-17-producing γδ T cells in a laser-induced choroidal neovascularization mouse model Chang, Yu-Hsien Hsing, Chung-Hsi Chiu, Chiao-Juno Wu, Yi-Rou Hsu, Sheng-Min Hsu, Yu-Hsiang J Neuroinflammation Research BACKGROUND: Vision loss in patients with wet/exudative age-related macular degeneration (AMD) is associated with choroidal neovascularization (CNV), and AMD is the leading cause of irreversible vision impairment in older adults. Interleukin-17A (IL-17A) is a component of the microenvironment associated with some autoimmune diseases. Previous studies have indicated that wet AMD patients have elevated serum IL-17A levels. However, the effect of IL-17A on AMD progression needs to be better understood. We aimed to investigate the role of IL-17A in a laser-induced CNV mouse model. METHODS: We established a laser-induced CNV mouse model in wild-type (WT) and IL-17A-deficient mice and then evaluated the disease severity of these mice by using fluorescence angiography. We performed enzyme-linked immunosorbent assay (ELISA) and fluorescence-activated cell sorting (FACS) to analyze the levels of IL-17A and to investigate the immune cell populations in the eyes of WT and IL-17A-deficient mice. We used ARPE-19 cells to clarify the effect of IL-17A under oxidative stress. RESULTS: In the laser-induced CNV model, the CNV lesions were larger in IL-17A-deficient mice than in WT mice. The numbers of γδ T cells, CD3(+)CD4(+)RORγt(+) T cells, Treg cells, and neutrophils were decreased and the number of macrophages was increased in the eyes of IL-17A-deficient mice compared with WT mice. In WT mice, IL-17A-producing γδ T-cell numbers increased in a time-dependent manner from day 7 to 28 after laser injury. IL-6 levels increased and IL-10, IL-24, IL-17F, and GM-CSF levels decreased in the eyes of IL-17A-deficient mice after laser injury. In vitro, IL-17A inhibited apoptosis and induced the expression of the antioxidant protein HO-1 in ARPE-19 cells under oxidative stress conditions. IL-17A facilitated the repair of oxidative stress-induced barrier dysfunction in ARPE-19 cells. CONCLUSIONS: Our findings provide new insight into the protective effect of IL-17A in a laser-induced CNV model and reveal a novel regulatory role of IL-17A-producing γδ T cells in the ocular microenvironment in wet AMD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-023-02952-1. BioMed Central 2023-11-25 /pmc/articles/PMC10676594/ /pubmed/38007487 http://dx.doi.org/10.1186/s12974-023-02952-1 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chang, Yu-Hsien
Hsing, Chung-Hsi
Chiu, Chiao-Juno
Wu, Yi-Rou
Hsu, Sheng-Min
Hsu, Yu-Hsiang
Protective role of IL-17-producing γδ T cells in a laser-induced choroidal neovascularization mouse model
title Protective role of IL-17-producing γδ T cells in a laser-induced choroidal neovascularization mouse model
title_full Protective role of IL-17-producing γδ T cells in a laser-induced choroidal neovascularization mouse model
title_fullStr Protective role of IL-17-producing γδ T cells in a laser-induced choroidal neovascularization mouse model
title_full_unstemmed Protective role of IL-17-producing γδ T cells in a laser-induced choroidal neovascularization mouse model
title_short Protective role of IL-17-producing γδ T cells in a laser-induced choroidal neovascularization mouse model
title_sort protective role of il-17-producing γδ t cells in a laser-induced choroidal neovascularization mouse model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676594/
https://www.ncbi.nlm.nih.gov/pubmed/38007487
http://dx.doi.org/10.1186/s12974-023-02952-1
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