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. Author manuscript; available in PMC: 2020 May 21.
Published in final edited form as: Immunity. 2019 Apr 2;50(5):1249–1261.e5. doi: 10.1016/j.immuni.2019.03.002

Figure 5. Skin-homing memory cells are decreased in Itgb6−/−Itgb8ΔKC mice.

Figure 5.

(A and B) Splenic B8R+ cells from WT or Itgb6−/−Itgb8ΔKC mice were analyzed for memory subsets based on expression of CXCR3 and CX3XR1 by flow cytometry at day 68 post skin vaccinia virus (VV) infection: CXCR3+CX3CR1 Tcm cells, CXCR3+CX3CR1int Tpm cells and CXCR3CX3CR1high Tem cells. (A) Representative flow cytometry plots gated on B8R+ cells and the (B, left panel) frequency and (B, right panel) number of each memory subset of B8R+ cells are shown. (C and D) E-selectin or P-selectin binding (ESL+ or PSL+ respectively) of splenic B8R+ cells were analyzed by flow cytometry following skin VV infection. Representative flow plots (C) and the frequency of ESL+ (top panels) or PSL+ (bottom panels) B8R+ cells day 7 and 68 post infection are shown. (D) Frequency of ESL+ (top panels) or PSL+ (bottom panels) among each subset of memory B8R+ cells in the spleen are shown. Data are representative of two separate experiments. Each dot represents an individual mouse. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001. See also Figure S6.