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. 1997 Jan 20;185(2):197–206. doi: 10.1084/jem.185.2.197

Figure 2.

Figure 2

Both wild-type Jak3 transgenes reconstitute T cell, but not B cell, development in Jak3 −/− mice. (A) The bone marrow, thymus, and spleen cells of Jak3 +/−, Jak3 −/−, Jak3 −/− (tgkd), and 35-d-old Jak3 −/− (tgthy+spl) and Jak3 −/− (tgthy) mice were stained with the indicated antibodies and analyzed by flow cytometry. Staining is shown on a logarithmic scale of fluorescence intensity. Numbers in the quadrants indicate subpopulation percentages. The dot plots are representative of average staining profiles, although some Jak3 −/− individuals had greatly increased CD4+/CD8+ ratios in the thymus and spleen. (B) The total cellularity of bone marrow, thymus, and spleen of mice analyzed in these experiments is indicated. For each organ, Jak3 +/−, lane 1; Jak3 −/−, lane 2; Jak3 −/− (tgthy+spl), lane 3; Jak3 −/− (tgthy), lane 4; and Jak3 −/− (tgkd), lane 5 are shown. Note the reconstitution of normal thymocyte cellularity by both wild-type, but not the kinase-dead, Jak3 transgenes. Data shown are representative of greater than six independent experiments.