Figure 5
Figure 5. CD4 and CD8 TMs home to tissues that supply them with their favored homeostatic cytokines. (A) Cytokine receptor expression on the MP CD4 and CD8 TMs (gated as CD4+CD25−CD44hi and CD8+CD44hi, respectively) in the spleen of 1-year-old B6 mice measured by flow cytometry. Representative histogram plots and mean fluorescence intensity (MFI) measurements are shown (n > 4). (B) Proliferation of CD4 and CD8 TMs in response to cytokine stimulation (100 ng/mL) for 3 days in vitro measured by cell counts. TMs were purified from 1-year-old B6 mice. Representative data are presented as mean of triplicates ± SEM (n = 4). (C,D) Proliferation of CD4 and CD8 TMs in response to cytokine stimulation in vivo measured by BLI. MFG-labeled OT2 (CD4) or OT1 (CD8) TEs (1 × 106) were adoptively transferred into each albino B6 recipient mouse. Six months later, the recipients harboring the OT2 or OT1 TMs received administration (IP) of either IL-7 or IL-15 daily (10 μg) for 5 sequential days. (C) Time-course tracking of the TBL change of the indicated recipient mice receiving either IL-7 or IL-15. Data are presented as mean ± SEM. (D) Representative BLI images of the indicated mice right before the 1st cytokine administration (day 1) and 1 day after the last cytokine administration (day 6; n = 3-4). (E) Tissue expression of IL-7 and IL-15 in 1-year-old B6 mice measured by Taqman Q-PCR. Representative data are presented as mean of triplicates ± SEM (n = 4).

CD4 and CD8 TMs home to tissues that supply them with their favored homeostatic cytokines. (A) Cytokine receptor expression on the MP CD4 and CD8 TMs (gated as CD4+CD25CD44hi and CD8+CD44hi, respectively) in the spleen of 1-year-old B6 mice measured by flow cytometry. Representative histogram plots and mean fluorescence intensity (MFI) measurements are shown (n > 4). (B) Proliferation of CD4 and CD8 TMs in response to cytokine stimulation (100 ng/mL) for 3 days in vitro measured by cell counts. TMs were purified from 1-year-old B6 mice. Representative data are presented as mean of triplicates ± SEM (n = 4). (C,D) Proliferation of CD4 and CD8 TMs in response to cytokine stimulation in vivo measured by BLI. MFG-labeled OT2 (CD4) or OT1 (CD8) TEs (1 × 106) were adoptively transferred into each albino B6 recipient mouse. Six months later, the recipients harboring the OT2 or OT1 TMs received administration (IP) of either IL-7 or IL-15 daily (10 μg) for 5 sequential days. (C) Time-course tracking of the TBL change of the indicated recipient mice receiving either IL-7 or IL-15. Data are presented as mean ± SEM. (D) Representative BLI images of the indicated mice right before the 1st cytokine administration (day 1) and 1 day after the last cytokine administration (day 6; n = 3-4). (E) Tissue expression of IL-7 and IL-15 in 1-year-old B6 mice measured by Taqman Q-PCR. Representative data are presented as mean of triplicates ± SEM (n = 4).

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