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. 2021 Apr 29;218(6):e20200940. doi: 10.1084/jem.20200940

Figure S1.

Figure S1.

Ptpn2 regulates early epidermal infiltration of OT-I cells independently of local antigen. (A) In vitro activated Ptpn2fl/fl and Lck-Cre;Ptpn2fl/fl OT-I cells were cultured with IL-2 (25 U/ml) in the presence or absence (Ctrl) of TGFβ (10 ng/ml), as indicated. Analysis of CD103 expression 2 d after addition of TGFβ; data are representative of n = 2 experiments. (B) Enumeration of CD103+ Ptpn2fl/fl (white) or Lck-Cre;Ptpn2fl/fl (orange) OT-I cells in epidermis and dermis in HSV-Ova (left flank)– and WT HSV (right flank)–infected skin 9 d after infection. Data were pooled from n = 2 experiments with n = 7 mice/group. (C and D) Means of KLRG1 OT-I cell numbers in spleen (C) and skin (D) from individual experiments 9 d after single or double HSV infection as in Fig. 1 H; data points from the same individual experiments (n = 7) connected by lines. Statistical significance (*, P < 0.05) determined by Wilcoxon test. (E) In vitro activated gBT-I cells transduced with pMIG.Klrg1.WT (left, middle) or pMIG.Ctrl (right) were cultured with IL-2 (25 U/ml) in the presence or absence (Ctrl) of TGFβ (10 ng/ml), as indicated. Analysis of KLRG1 and CD103 expression by GFP+ gBT-I cells 3 d after addition of TGFβ; data are representative of n = 2 experiments.