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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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 |
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. |
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