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. 2019 Nov 13;217(2):e20190969. doi: 10.1084/jem.20190969

Figure S3.

Figure S3.

Signaling events in Pggt1b−/− thymocyte and homeostasis of Fntb−/− mice. (A) Immunoblot analysis of p-Pak1/2 and Tiam1 in semimature CD4SP thymocytes from WT and Pggt1b−/− mice upon CCL19 stimulation. (B) Immunoblot analysis of p-Mob1 in mature CD4SP thymocytes from WT and Pggt1b−/− mice upon CCL19 stimulation. (C) Immunoblot analysis of p-Pak1/2 or p-Foxo1/3a in semimature CD4SP thymocytes from WT mice upon CCL19 or anti-CD3/28 stimulation. (D) Immunoblot analysis of Hdj-2 in mature CD4SP thymocytes from WT and Fntb−/− mice. (E) Immunoblot analysis of p-Pak1/2 and Tiam1 in mature CD4SP thymocytes from WT and Fntb−/− mice upon CCL19 stimulation. (F) Frequencies (left) and numbers (right) of CD4+ T cells and CD8+ T cells in PLN of WT and Fntb−/− mice. (G) Frequencies of CD44loCD62Lhi naive (left) and CD44hiCD62Llo effector/memory (right) cells in CD4+ or CD8+ T cells from PLNs of WT and Fntb−/− mice. (H) Frequencies of Ki-67+ (left) and active caspase-3+ (right) cells in CD4+ or CD8+ T cells from PLNs of WT and Fntb−/− mice. (I) Expression of CD44 and CD69, as indicated by MFI, on WT and Fntb−/− naive CD4+ T cells upon overnight stimulation with plate-bound anti-CD3/28 (n = 9 per genotype). Data are shown as mean ± SEM. *, P < 0.05; **, P < 0.01; two-tailed unpaired Student’s t test in F–I. Data are from two (A–D) or four (F–H) independent experiments.