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. Author manuscript; available in PMC: 2011 Aug 27.
Published in final edited form as: Immunity. 2010 Jul 30;33(2):203–215. doi: 10.1016/j.immuni.2010.07.013

Figure 3.

Figure 3

Id3−/ − innate-like CD8 T cells were selected on non-hematopoietic cells. (A–D) Flow cytometric analysis of thymocytes derived from chimeric mice 6 weeks after transplantation. (A and C) CD4 and CD8 expression on total thymocytes (upper panels), TCRβ expression on total thymocytes (middle panels) and CD4 and CD8 expression on TCRβ + thymocytes (lower panels). Expression of CD122, CD44 or CD24 on TCRβ +CD8 thymocytes in (B) WT to B2m−/ − chimeras (grey) or Id3−/ − to B2m−/ − chimeras (black) or (D) H2-KbH2-Db/ to WT (grey) or Id3/ H2-KbH2-Db/ to WT chimeras. (E) Average number (+ standard deviation) of CD122+TCRβ +CD8 thymocytes in chimeric mice from the indicated donor and recipient combinations. n> 3 for each combination. P-values are shown for populations at the end of each line. Three independent experiments were performed. See Figure S2 for analysis of the innate-like phenotype on Id3−/ − to WT chimeras.