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. Author manuscript; available in PMC: 2022 Aug 1.
Published in final edited form as: Cell Mol Life Sci. 2021 Jun 15;78(15):5789–5805. doi: 10.1007/s00018-021-03877-9

Figure 5. Phenotypic characterization of CD103Tg CD4 T cells.

Figure 5.

(A) LN T cell frequency and numbers in 2D2 and 2D2.CD103Tgβ7Tg mice. The histogram (left) is representative (left) and the graph (right) is the summary of 4 independent experiments with 5 2D2 and 5 2D2.CD103Tgβ7Tg mice.

(B) Phenotype of 2D2 and 2D2.CD103Tgβ7Tg LN T cells. Naïve versus memory phenotype was assessed by CD44 versus CD62L staining in CD4 LN T cells (top) and by CD44 versus CD122 staining in CD8 LN T cells (bottom). Results are representative 3 independent experiments with 4 2D2 and 4 2D2.CD103Tgβ7Tg mice.

(C) CD4 versus CD8 profiles of TCRβ+-gated LN T cells from WT and CD103Tgβ7Tg mice (left). The bar graph shows CD4 T cell frequencies from LNs of WT and CD103Tgβ7Tg mice (right). The results show the summary of 8 independent experiments with a total of 9 WT and 9 CD103Tgβ7Tg mice.

(D) CD103 and β7 expression were determined on CD4 LN T cells of the indicated mice (top). Histograms show staining of anti-CD103 or anti-β7 (shaded) versus isotype control antibody (open). Bar graphs show the ΔMFI of CD103 and β7 on CD4 LN T cells of the indicated mice (bottom). The results are a summary of 4 independent experiments with a total of 4 WT and 4 CD103Tgβ7Tg mice.

(E) Frequency of Foxp3+ Treg cells in the thymus, LN, and spleen of WT and CD103Tgβ7Tg mice. The results are representative of 6 independent experiments with a total of 6 WT and 6 CD103Tgβ7Tg mice.