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Characterization of γδT cells in lung of Plasmodium yoelii-infected C57BL/6 mice
BACKGROUND: Malaria has high morbidity and mortality rates in some parts of tropical and subtropical countries. Besides respiratory and metabolic function, lung plays a role in immune system. γδT cells have multiple functions in producing cytokines and chemokines, regulating the immune response by i...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885449/ https://www.ncbi.nlm.nih.gov/pubmed/33588839 http://dx.doi.org/10.1186/s12936-021-03619-z |
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author | Wei, Haixia Jin, Chenxi Peng, Anping Xie, Hongyan Xie, Shihao Feng, Yuanfa Xie, Anqi Li, Jiajie Fang, Chao Yang, Quan Qiu, Huaina Qi, Yanwei Yin, Zhinan Wang, Xinhua Huang, Jun |
author_facet | Wei, Haixia Jin, Chenxi Peng, Anping Xie, Hongyan Xie, Shihao Feng, Yuanfa Xie, Anqi Li, Jiajie Fang, Chao Yang, Quan Qiu, Huaina Qi, Yanwei Yin, Zhinan Wang, Xinhua Huang, Jun |
author_sort | Wei, Haixia |
collection | PubMed |
description | BACKGROUND: Malaria has high morbidity and mortality rates in some parts of tropical and subtropical countries. Besides respiratory and metabolic function, lung plays a role in immune system. γδT cells have multiple functions in producing cytokines and chemokines, regulating the immune response by interacting with other cells. It remains unclear about the role of γδT cells in the lung of mice infected by malaria parasites. METHODS: Flow cytometry (FCM) was used to evaluate the frequency of γδT cells and the effects of γδT cells on the phenotype and function of B and T cells in Plasmodium yoelii-infected wild-type (WT) or γδTCR knockout (γδT KO) mice. Haematoxylin-eosin (HE) staining was used to observe the pathological changes in the lungs. RESULTS: The percentage and absolute number of γδT cells in the lung increased after Plasmodium infection (p < 0.01). More γδT cells were expressing CD80, CD11b, or PD-1 post-infection (p < 0.05), while less γδT cells were expressing CD34, CD62L, and CD127 post-infection (p < 0.05). The percentages of IL-4(+), IL-5(+), IL-6(+), IL-21(+), IL-1α(+), and IL-17(+) γδT cells were increased (p < 0.05), but the percentage of IFN-γ-expressing γδT cells decreased (p < 0.05) post-infection. The pathological changes in the lungs of the infected γδT KO mice were not obvious compared with the infected WT mice. The proportion of CD3(+) cells and absolute numbers of CD3(+) cells, CD3(+) CD4(+) cells, CD3(+) CD8(+) cells decreased in γδT KO infected mice (p < 0.05). γδT KO infected mice exhibited no significant difference in the surface molecular expression of T cells compared with the WT infected mice (p > 0.05). While, the percentage of IFN-γ-expressing CD3(+) and CD3(+) CD8(+) cells increased in γδT KO infected mice (p < 0.05). There was no significant difference in the absolute numbers of the total, CD69(+), ICOS(+), and CD80(+) B cells between the WT infected and γδT KO infected mice (p > 0.05). CONCLUSIONS: The content, phenotype, and function of γδT cells in the lung of C57BL/6 mice were changed after Plasmodium infection. γδT cells contribute to T cell immune response in the progress of Plasmodium infection. |
format | Online Article Text |
id | pubmed-7885449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78854492021-02-17 Characterization of γδT cells in lung of Plasmodium yoelii-infected C57BL/6 mice Wei, Haixia Jin, Chenxi Peng, Anping Xie, Hongyan Xie, Shihao Feng, Yuanfa Xie, Anqi Li, Jiajie Fang, Chao Yang, Quan Qiu, Huaina Qi, Yanwei Yin, Zhinan Wang, Xinhua Huang, Jun Malar J Research BACKGROUND: Malaria has high morbidity and mortality rates in some parts of tropical and subtropical countries. Besides respiratory and metabolic function, lung plays a role in immune system. γδT cells have multiple functions in producing cytokines and chemokines, regulating the immune response by interacting with other cells. It remains unclear about the role of γδT cells in the lung of mice infected by malaria parasites. METHODS: Flow cytometry (FCM) was used to evaluate the frequency of γδT cells and the effects of γδT cells on the phenotype and function of B and T cells in Plasmodium yoelii-infected wild-type (WT) or γδTCR knockout (γδT KO) mice. Haematoxylin-eosin (HE) staining was used to observe the pathological changes in the lungs. RESULTS: The percentage and absolute number of γδT cells in the lung increased after Plasmodium infection (p < 0.01). More γδT cells were expressing CD80, CD11b, or PD-1 post-infection (p < 0.05), while less γδT cells were expressing CD34, CD62L, and CD127 post-infection (p < 0.05). The percentages of IL-4(+), IL-5(+), IL-6(+), IL-21(+), IL-1α(+), and IL-17(+) γδT cells were increased (p < 0.05), but the percentage of IFN-γ-expressing γδT cells decreased (p < 0.05) post-infection. The pathological changes in the lungs of the infected γδT KO mice were not obvious compared with the infected WT mice. The proportion of CD3(+) cells and absolute numbers of CD3(+) cells, CD3(+) CD4(+) cells, CD3(+) CD8(+) cells decreased in γδT KO infected mice (p < 0.05). γδT KO infected mice exhibited no significant difference in the surface molecular expression of T cells compared with the WT infected mice (p > 0.05). While, the percentage of IFN-γ-expressing CD3(+) and CD3(+) CD8(+) cells increased in γδT KO infected mice (p < 0.05). There was no significant difference in the absolute numbers of the total, CD69(+), ICOS(+), and CD80(+) B cells between the WT infected and γδT KO infected mice (p > 0.05). CONCLUSIONS: The content, phenotype, and function of γδT cells in the lung of C57BL/6 mice were changed after Plasmodium infection. γδT cells contribute to T cell immune response in the progress of Plasmodium infection. BioMed Central 2021-02-15 /pmc/articles/PMC7885449/ /pubmed/33588839 http://dx.doi.org/10.1186/s12936-021-03619-z Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://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 Wei, Haixia Jin, Chenxi Peng, Anping Xie, Hongyan Xie, Shihao Feng, Yuanfa Xie, Anqi Li, Jiajie Fang, Chao Yang, Quan Qiu, Huaina Qi, Yanwei Yin, Zhinan Wang, Xinhua Huang, Jun Characterization of γδT cells in lung of Plasmodium yoelii-infected C57BL/6 mice |
title | Characterization of γδT cells in lung of Plasmodium yoelii-infected C57BL/6 mice |
title_full | Characterization of γδT cells in lung of Plasmodium yoelii-infected C57BL/6 mice |
title_fullStr | Characterization of γδT cells in lung of Plasmodium yoelii-infected C57BL/6 mice |
title_full_unstemmed | Characterization of γδT cells in lung of Plasmodium yoelii-infected C57BL/6 mice |
title_short | Characterization of γδT cells in lung of Plasmodium yoelii-infected C57BL/6 mice |
title_sort | characterization of γδt cells in lung of plasmodium yoelii-infected c57bl/6 mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885449/ https://www.ncbi.nlm.nih.gov/pubmed/33588839 http://dx.doi.org/10.1186/s12936-021-03619-z |
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