Figure 3.
Figure 3. The extent of the memory phenotype of H-Y CD8 T cells determines their ability to respond to cytokines in vitro as well as their ability to undergo homeostatic expansion in vivo. (A) Purified CD8+ T cells from female H-2b H-Y (CD8hi), male H-2b H-Y (CD8lo), or male H-2b/d H-Y (CD8int) mice were labeled with CFSE and cultured with IL-2 (200 U/mL), IL-15 (100 ng/mL), or H-Y peptide (1 μM), B6-Tap1-/- splenocytes (1 × 107), and IL-2 (20 U/mL). Proliferation of gated H-Y TCRα+ CD8+ cells was analyzed by FACS at 48 (filled histogram), 72 (dark line), and 96 (light line) hours with each CFSE peak representing one cell division. (B) Purified CD8hi, CD8int, and CD8lo cells were CFSE labeled and transferred into sublethally irradiated B6 female (filled histogram) or male (unfilled histogram) recipients. CFSE profiles of gated CD8+ H-Y TCR+ cells 7 days after transfer are shown in the histograms.

The extent of the memory phenotype of H-Y CD8 T cells determines their ability to respond to cytokines in vitro as well as their ability to undergo homeostatic expansion in vivo. (A) Purified CD8+ T cells from female H-2b H-Y (CD8hi), male H-2b H-Y (CD8lo), or male H-2b/d H-Y (CD8int) mice were labeled with CFSE and cultured with IL-2 (200 U/mL), IL-15 (100 ng/mL), or H-Y peptide (1 μM), B6-Tap1-/- splenocytes (1 × 107), and IL-2 (20 U/mL). Proliferation of gated H-Y TCRα+ CD8+ cells was analyzed by FACS at 48 (filled histogram), 72 (dark line), and 96 (light line) hours with each CFSE peak representing one cell division. (B) Purified CD8hi, CD8int, and CD8lo cells were CFSE labeled and transferred into sublethally irradiated B6 female (filled histogram) or male (unfilled histogram) recipients. CFSE profiles of gated CD8+ H-Y TCR+ cells 7 days after transfer are shown in the histograms.

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