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. Author manuscript; available in PMC: 2020 Aug 15.
Published in final edited form as: J Immunol. 2019 Jun 24;203(4):936–945. doi: 10.4049/jimmunol.1900093

Figure 5. Phenotype of lung TRM cells is independent of TCR signal strength.

Figure 5

Challenged mice were generated as in Figure 1. (A) Representative flow plots of CD69 and CD103 staining on iv OT-I T cells in the lung and FRT on 10 and 34 dpi from mice. (B) The percentage of iv OT-I T cells expressing CD103+CD69, CD103+CD69+ or CD103CD69+ (C-F) On 34 dpi, lungs (C, D) and spleens (E, F) were harvested and cells were stimulated ex vivo with 1 μg/mL N4 peptide. As a positive control, cells were stimulated with PMA/Ionomycin. (C, E) Representative IFN-γ staining of iv lung (C) or total spleen (E) OT-I T cells unstimulated, stimulated with PMA/Ionomycin or N4 peptide. (D, F) Percentage of iv lung (D) or total spleen (F) IFN-γ+ OT-I T cells after ex vivo N4 stimulation. The results (B) are combined from 2 independent experiments with at least 3 mice per group, per experiment (± SEM). The results (D,F) are 1 representative experiment of 2 independent experiments with at least 5 mice per group, per experiment (± SEM). *p < 0.05, ** p < 0.01 (unpaired t test).