Figure 4
Figure 4. Activation of Bg1 CD8+ T cells in Tie2-LacZ mice. (A) A total of 1.5 × 107 CFSE-labeled splenocytes (corresponding to 3 × 106 CD8+ TCR-transgenic T cells) from Bg1 mice were adoptively transferred into C57BL/6 or Tie2-LacZ mice. Mice were killed on day 4 following transfer and cells from blood, spleen, and lymph nodes were analyzed by flow cytometry for CFSE dilution and CD44 up-regulation on CD8+ lymphocytes. Representative FACS plots from one representative of 2 independent experiments are shown. (B) Quantification of Bg1 T-cell proliferation. A total of 1.5 × 107 CFSE-labeled Bg1 Thy1.1+ splenocytes were injected into C57BL/6 or naive Tie2-LacZ mice. Mice were killed on day 4 following transfer and cells from blood, spleen, and lymph nodes were analyzed by flow cytometry. Values represent mean percentage (± SEM, n = 7; pooled data from 2 independent experiments) of proliferating CD8+Thy1.1+ cells (*P < .05; **P < .005; ***P < .001).

Activation of Bg1 CD8+ T cells in Tie2-LacZ mice. (A) A total of 1.5 × 107 CFSE-labeled splenocytes (corresponding to 3 × 106 CD8+ TCR-transgenic T cells) from Bg1 mice were adoptively transferred into C57BL/6 or Tie2-LacZ mice. Mice were killed on day 4 following transfer and cells from blood, spleen, and lymph nodes were analyzed by flow cytometry for CFSE dilution and CD44 up-regulation on CD8+ lymphocytes. Representative FACS plots from one representative of 2 independent experiments are shown. (B) Quantification of Bg1 T-cell proliferation. A total of 1.5 × 107 CFSE-labeled Bg1 Thy1.1+ splenocytes were injected into C57BL/6 or naive Tie2-LacZ mice. Mice were killed on day 4 following transfer and cells from blood, spleen, and lymph nodes were analyzed by flow cytometry. Values represent mean percentage (± SEM, n = 7; pooled data from 2 independent experiments) of proliferating CD8+Thy1.1+ cells (*P < .05; **P < .005; ***P < .001).

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