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Changes of CD103-expressing pulmonary CD4(+) and CD8(+) T cells in S. japonicum infected C57BL/6 mice

BACKGROUND: Recent studies have shown that CD103 is an important marker for tissue-resident memory T cells (TRM) which plays an important role in anti-infection. However, the role of CD103(+) TRM was not elucidated in the progress of S. japonicum infection induced disease. METHODS: 6–8 weeks old C57...

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Detalles Bibliográficos
Autores principales: Zhao, Yi, Yang, Quan, Jin, Chenxi, Feng, Yuanfa, Xie, Shihao, Xie, Hongyan, Qi, Yanwei, Qiu, Huaina, Chen, Hongyuan, Tao, Ailin, Mu, Jianbing, Qin, Wenjuan, Huang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880605/
https://www.ncbi.nlm.nih.gov/pubmed/31775660
http://dx.doi.org/10.1186/s12879-019-4633-8
Descripción
Sumario:BACKGROUND: Recent studies have shown that CD103 is an important marker for tissue-resident memory T cells (TRM) which plays an important role in anti-infection. However, the role of CD103(+) TRM was not elucidated in the progress of S. japonicum infection induced disease. METHODS: 6–8 weeks old C57BL/6 mice were infected by S. japonicum. Mice were sacrificed and the lungs were removed 5–6 weeks after infection. Immunofluorescent staining and Q-PCR were performed to identify the expression of CD103 molecule. Single cellular populations were made, percentages of CD103 on both CD4(+) and CD8(+) T lymphocytes were dynamical observed by flow cytometry (FCM). Moreover, the expression of memory T cells related molecules CD69 and CD62L, T cell function associated molecules CD107a, IFN-γ, IL-4, IL-9, and IL-10 were compared between CD103(+) CD4(+) and CD8(+) T cells by FCM. RESULTS: CD103(+) cells were emerged in the lung of both naive and S. japonicum infected mice. Both the percentage and the absolute numbers of pulmonary CD4(+) and CD8(+) cells were increased after S. japonicum infection (P < 0.05). The percentage of CD103(+) cells in CD8(+) T cells decreased significantly at the early stage of S. japonicum infection (P < 0.05). Increased CD69, decreased CD62L and CD107a expressions were detected on both CD4(+) and CD8(+) CD103(+) T cells in the lungs of infected mice (P < 0.05). Compared to CD8(+) CD103(+) T cells, CD4(+) CD103(+) T cells from infected mice expressed higher level of CD69 and lower level CD62L molecules (P < 0.05). Moreover, higher percentage of IL-4(+), IL-9(+) and IL-10(+) cells on CD4(+) CD103(+) pulmonary T cells was found in infected mice (P < 0.05). Significantly increased IL-4 and IL-9, and decreased IFN-γ expressing cells were detected in CD8(+)CD103(+) cells of infected mice (P < 0.05). CONCLUSIONS: CD103-expressing pulmonary CD4(+) and CD8(+) T cells play important roles in mediating S. japonicum infection induced granulomatous inflammation in the lung.