Fig. 10.
Fig. 10. Enrichment of CD4+ TNK cells in TLI-treated mice. / (A) FACS contour plots of gated CD4+ spleen cells from a day-2 post–TLI-treated mouse (left) and a control mouse (right). The numbers in the boxed areas indicate the percentages of CD4+cells expressing either CD44hi/IL-2Rβ+ or CD44lo/IL-2Rβ−. Analysis was restricted to live cells by propidium iodine exclusion. Data are from 1 of 5 representative experiments. (B) Spleen cells from 2-day post–TLI-treated mice were analyzed for CD4, CD44, IL-2Rβ, and specific Vβ expression using 4-color FACS. Error bars represent the mean ± SE of the relative number of CD44hi/IL-Rβ+ (open bar) or CD44lo/IL-2Rβ− (hatched bars) CD4 cells that stain with Vβ 8.1, 8.2, 8.3, or Vβ 8.3 from 3 separate experiments. For each experiment, 3 to 5 spleens were pulled from TLI-treated mice.

Enrichment of CD4+ TNK cells in TLI-treated mice.

(A) FACS contour plots of gated CD4+ spleen cells from a day-2 post–TLI-treated mouse (left) and a control mouse (right). The numbers in the boxed areas indicate the percentages of CD4+cells expressing either CD44hi/IL-2Rβ+ or CD44lo/IL-2Rβ. Analysis was restricted to live cells by propidium iodine exclusion. Data are from 1 of 5 representative experiments. (B) Spleen cells from 2-day post–TLI-treated mice were analyzed for CD4, CD44, IL-2Rβ, and specific Vβ expression using 4-color FACS. Error bars represent the mean ± SE of the relative number of CD44hi/IL-Rβ+ (open bar) or CD44lo/IL-2Rβ (hatched bars) CD4 cells that stain with Vβ 8.1, 8.2, 8.3, or Vβ 8.3 from 3 separate experiments. For each experiment, 3 to 5 spleens were pulled from TLI-treated mice.

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