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Mesangial Cells Exhibit Features of Antigen-Presenting Cells and Activate CD4+ T Cell Responses

BACKGROUND: Mesangial cells play a prominent role in the development of inflammatory diseases and autoimmune disorders of the kidney. Mesangial cells perform the essential functions of helping to ensure that the glomerular structure is stable and regulating capillary flow, and activated mesangial ce...

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Autores principales: Yu, Hongyu, Cui, Shaoyuan, Mei, Yan, Li, Qinggang, Wu, Lingling, Duan, Shuwei, Cai, Guangyan, Zhu, Hanyu, Fu, Bo, Zhang, Li, Feng, Zhe, Chen, Xiangmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604415/
https://www.ncbi.nlm.nih.gov/pubmed/31317046
http://dx.doi.org/10.1155/2019/2121849
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author Yu, Hongyu
Cui, Shaoyuan
Mei, Yan
Li, Qinggang
Wu, Lingling
Duan, Shuwei
Cai, Guangyan
Zhu, Hanyu
Fu, Bo
Zhang, Li
Feng, Zhe
Chen, Xiangmei
author_facet Yu, Hongyu
Cui, Shaoyuan
Mei, Yan
Li, Qinggang
Wu, Lingling
Duan, Shuwei
Cai, Guangyan
Zhu, Hanyu
Fu, Bo
Zhang, Li
Feng, Zhe
Chen, Xiangmei
author_sort Yu, Hongyu
collection PubMed
description BACKGROUND: Mesangial cells play a prominent role in the development of inflammatory diseases and autoimmune disorders of the kidney. Mesangial cells perform the essential functions of helping to ensure that the glomerular structure is stable and regulating capillary flow, and activated mesangial cells acquire proinflammatory activities. We investigated whether activated mesangial cells display immune properties and control the development of T cell immunity. METHODS: Flow cytometry analysis was used to study the expression of antigen-presenting cell surface markers and costimulatory molecules in mesangial cells. CD4+ T cell activation induced by mesangial cells was detected in terms of T cell proliferation and cytokine production. RESULTS: IFN-γ-treated mesangial cells express membrane proteins involved in antigen presentation and T cell activation, including MHC-II, ICAM-1, CD40, and CD80. This finding suggests that activated mesangial cells can take up and present antigenic peptides to initiate CD4+ T cell responses and thus act as nonprofessional antigen-presenting cells. Polarization of naïve CD4+ T cells (Th0 cells) towards the Th1 phenotype was induced by coculture with activated mesangial cells, and the resulting Th1 cells showed increased mRNA and protein expression of inflammation-associated genes. CONCLUSION: Mesangial cells can present antigen and modulate CD4+ T lymphocyte proliferation and differentiation. Interactions between mesangial cells and T cells are essential for sustaining the inflammatory response in a variety of glomerulonephritides. Therefore, mesangial cells might participate in immune function in the kidney.
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spelling pubmed-66044152019-07-17 Mesangial Cells Exhibit Features of Antigen-Presenting Cells and Activate CD4+ T Cell Responses Yu, Hongyu Cui, Shaoyuan Mei, Yan Li, Qinggang Wu, Lingling Duan, Shuwei Cai, Guangyan Zhu, Hanyu Fu, Bo Zhang, Li Feng, Zhe Chen, Xiangmei J Immunol Res Research Article BACKGROUND: Mesangial cells play a prominent role in the development of inflammatory diseases and autoimmune disorders of the kidney. Mesangial cells perform the essential functions of helping to ensure that the glomerular structure is stable and regulating capillary flow, and activated mesangial cells acquire proinflammatory activities. We investigated whether activated mesangial cells display immune properties and control the development of T cell immunity. METHODS: Flow cytometry analysis was used to study the expression of antigen-presenting cell surface markers and costimulatory molecules in mesangial cells. CD4+ T cell activation induced by mesangial cells was detected in terms of T cell proliferation and cytokine production. RESULTS: IFN-γ-treated mesangial cells express membrane proteins involved in antigen presentation and T cell activation, including MHC-II, ICAM-1, CD40, and CD80. This finding suggests that activated mesangial cells can take up and present antigenic peptides to initiate CD4+ T cell responses and thus act as nonprofessional antigen-presenting cells. Polarization of naïve CD4+ T cells (Th0 cells) towards the Th1 phenotype was induced by coculture with activated mesangial cells, and the resulting Th1 cells showed increased mRNA and protein expression of inflammation-associated genes. CONCLUSION: Mesangial cells can present antigen and modulate CD4+ T lymphocyte proliferation and differentiation. Interactions between mesangial cells and T cells are essential for sustaining the inflammatory response in a variety of glomerulonephritides. Therefore, mesangial cells might participate in immune function in the kidney. Hindawi 2019-06-17 /pmc/articles/PMC6604415/ /pubmed/31317046 http://dx.doi.org/10.1155/2019/2121849 Text en Copyright © 2019 Hongyu Yu et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yu, Hongyu
Cui, Shaoyuan
Mei, Yan
Li, Qinggang
Wu, Lingling
Duan, Shuwei
Cai, Guangyan
Zhu, Hanyu
Fu, Bo
Zhang, Li
Feng, Zhe
Chen, Xiangmei
Mesangial Cells Exhibit Features of Antigen-Presenting Cells and Activate CD4+ T Cell Responses
title Mesangial Cells Exhibit Features of Antigen-Presenting Cells and Activate CD4+ T Cell Responses
title_full Mesangial Cells Exhibit Features of Antigen-Presenting Cells and Activate CD4+ T Cell Responses
title_fullStr Mesangial Cells Exhibit Features of Antigen-Presenting Cells and Activate CD4+ T Cell Responses
title_full_unstemmed Mesangial Cells Exhibit Features of Antigen-Presenting Cells and Activate CD4+ T Cell Responses
title_short Mesangial Cells Exhibit Features of Antigen-Presenting Cells and Activate CD4+ T Cell Responses
title_sort mesangial cells exhibit features of antigen-presenting cells and activate cd4+ t cell responses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604415/
https://www.ncbi.nlm.nih.gov/pubmed/31317046
http://dx.doi.org/10.1155/2019/2121849
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