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Dynamic Profile of CD4(+) T-Cell-Associated Cytokines/Chemokines following Murine Myocardial Infarction/Reperfusion

CD4(+) T-cells play crucial roles in the injured heart. However, the way in which different CD4(+) T subtypes function in the myocardial infarction/reperfusion (MI/R) heart is still poorly understood. We aimed to detect the dynamic profile of distinct CD4(+) subpopulation-associated cytokines/chemok...

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Autores principales: Yuan, Dongsheng, Tie, Jinjun, Xu, Zhican, Liu, Guanya, Ge, Xinyu, Wang, Zhulin, Zhang, Xumin, Gong, Shiyu, Liu, Gang, Meng, Qingshu, Lin, Fang, Liu, Zhongmin, Fan, Huimin, Zhou, Xiaohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442492/
https://www.ncbi.nlm.nih.gov/pubmed/31011288
http://dx.doi.org/10.1155/2019/9483647
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author Yuan, Dongsheng
Tie, Jinjun
Xu, Zhican
Liu, Guanya
Ge, Xinyu
Wang, Zhulin
Zhang, Xumin
Gong, Shiyu
Liu, Gang
Meng, Qingshu
Lin, Fang
Liu, Zhongmin
Fan, Huimin
Zhou, Xiaohui
author_facet Yuan, Dongsheng
Tie, Jinjun
Xu, Zhican
Liu, Guanya
Ge, Xinyu
Wang, Zhulin
Zhang, Xumin
Gong, Shiyu
Liu, Gang
Meng, Qingshu
Lin, Fang
Liu, Zhongmin
Fan, Huimin
Zhou, Xiaohui
author_sort Yuan, Dongsheng
collection PubMed
description CD4(+) T-cells play crucial roles in the injured heart. However, the way in which different CD4(+) T subtypes function in the myocardial infarction/reperfusion (MI/R) heart is still poorly understood. We aimed to detect the dynamic profile of distinct CD4(+) subpopulation-associated cytokines/chemokines by relying on a closed-chest acute murine MI/R model. The protein levels of 26 CD4(+) T-cell-associated cytokines/chemokines were detected in the heart tissues and serum of mice at day 7 and day 14 post-MI/R or sham surgery. The mRNA levels of IL-4, IL-6, IL-13, IL-27, MIP-1β, MCP-3, and GRO-α were measured in blood mononuclear cells. The protein levels of IL-4, IL-6, IL-13, IL-27, MIP-1β, MCP-3, and GRO-α increased in both injured heart tissues and serum, while IFN-γ, IL-12P70, IL-2, IL-1β, IL-18, TNF-α, IL-5, IL-9, IL-17A, IL-23, IL-10, eotaxin, MIP-1α, RANTES, MCP-1, and MIP-2 increased only in MI/R heart tissues in the day 7 and day 14 groups compared to the sham group. In serum, the IFN-γ, IL-23, and IL-10 levels were downregulated in the MI/R model at both day 7 and day 14 compared to the sham. Compared with the protein expressions in injured heart tissues at day 7, IFN-γ, IL-12P70, IL-2, IL-18, TNF-α, IL-6, IL-4, IL-5, IL-9, IL-17A, IL-23, IL-27, IL-10, eotaxin, IP-10, RANTES, MCP-1, MCP-3, and GRO-α were reduced, while IL-1β and MIP-2 were elevated at day 14. IL-13 and MIP-1β showed higher levels in the MI/R serum at day 14 than at day 7. mRNA levels of IL-4, IL-6, IL-13, and IL-27 were increased in the day 7 group compared to the sham, while MIP-1β, MCP-3, and GRO-α mRNA levels showed no significant difference between the MI/R and sham groups in blood mononuclear cells. Multiple CD4(+) T-cell-associated cytokines/chemokines were upregulated in the MI/R hearts at the chronic stage. These results provided important evidence necessary for developing future immunomodulatory therapies after MI/R.
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spelling pubmed-64424922019-04-22 Dynamic Profile of CD4(+) T-Cell-Associated Cytokines/Chemokines following Murine Myocardial Infarction/Reperfusion Yuan, Dongsheng Tie, Jinjun Xu, Zhican Liu, Guanya Ge, Xinyu Wang, Zhulin Zhang, Xumin Gong, Shiyu Liu, Gang Meng, Qingshu Lin, Fang Liu, Zhongmin Fan, Huimin Zhou, Xiaohui Mediators Inflamm Research Article CD4(+) T-cells play crucial roles in the injured heart. However, the way in which different CD4(+) T subtypes function in the myocardial infarction/reperfusion (MI/R) heart is still poorly understood. We aimed to detect the dynamic profile of distinct CD4(+) subpopulation-associated cytokines/chemokines by relying on a closed-chest acute murine MI/R model. The protein levels of 26 CD4(+) T-cell-associated cytokines/chemokines were detected in the heart tissues and serum of mice at day 7 and day 14 post-MI/R or sham surgery. The mRNA levels of IL-4, IL-6, IL-13, IL-27, MIP-1β, MCP-3, and GRO-α were measured in blood mononuclear cells. The protein levels of IL-4, IL-6, IL-13, IL-27, MIP-1β, MCP-3, and GRO-α increased in both injured heart tissues and serum, while IFN-γ, IL-12P70, IL-2, IL-1β, IL-18, TNF-α, IL-5, IL-9, IL-17A, IL-23, IL-10, eotaxin, MIP-1α, RANTES, MCP-1, and MIP-2 increased only in MI/R heart tissues in the day 7 and day 14 groups compared to the sham group. In serum, the IFN-γ, IL-23, and IL-10 levels were downregulated in the MI/R model at both day 7 and day 14 compared to the sham. Compared with the protein expressions in injured heart tissues at day 7, IFN-γ, IL-12P70, IL-2, IL-18, TNF-α, IL-6, IL-4, IL-5, IL-9, IL-17A, IL-23, IL-27, IL-10, eotaxin, IP-10, RANTES, MCP-1, MCP-3, and GRO-α were reduced, while IL-1β and MIP-2 were elevated at day 14. IL-13 and MIP-1β showed higher levels in the MI/R serum at day 14 than at day 7. mRNA levels of IL-4, IL-6, IL-13, and IL-27 were increased in the day 7 group compared to the sham, while MIP-1β, MCP-3, and GRO-α mRNA levels showed no significant difference between the MI/R and sham groups in blood mononuclear cells. Multiple CD4(+) T-cell-associated cytokines/chemokines were upregulated in the MI/R hearts at the chronic stage. These results provided important evidence necessary for developing future immunomodulatory therapies after MI/R. Hindawi 2019-03-18 /pmc/articles/PMC6442492/ /pubmed/31011288 http://dx.doi.org/10.1155/2019/9483647 Text en Copyright © 2019 Dongsheng Yuan 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
Yuan, Dongsheng
Tie, Jinjun
Xu, Zhican
Liu, Guanya
Ge, Xinyu
Wang, Zhulin
Zhang, Xumin
Gong, Shiyu
Liu, Gang
Meng, Qingshu
Lin, Fang
Liu, Zhongmin
Fan, Huimin
Zhou, Xiaohui
Dynamic Profile of CD4(+) T-Cell-Associated Cytokines/Chemokines following Murine Myocardial Infarction/Reperfusion
title Dynamic Profile of CD4(+) T-Cell-Associated Cytokines/Chemokines following Murine Myocardial Infarction/Reperfusion
title_full Dynamic Profile of CD4(+) T-Cell-Associated Cytokines/Chemokines following Murine Myocardial Infarction/Reperfusion
title_fullStr Dynamic Profile of CD4(+) T-Cell-Associated Cytokines/Chemokines following Murine Myocardial Infarction/Reperfusion
title_full_unstemmed Dynamic Profile of CD4(+) T-Cell-Associated Cytokines/Chemokines following Murine Myocardial Infarction/Reperfusion
title_short Dynamic Profile of CD4(+) T-Cell-Associated Cytokines/Chemokines following Murine Myocardial Infarction/Reperfusion
title_sort dynamic profile of cd4(+) t-cell-associated cytokines/chemokines following murine myocardial infarction/reperfusion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442492/
https://www.ncbi.nlm.nih.gov/pubmed/31011288
http://dx.doi.org/10.1155/2019/9483647
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