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. 2012 Aug;136(4):437–447. doi: 10.1111/j.1365-2567.2012.03600.x

Figure 2.

Figure 2

Transgenic mice with Cre recombinase under the control of the endogenous OX40 promoter were crossed with GFP reporter mice to generate F1 mice that show stable expression of GFP in cells that have expressed OX40. OX40Cre+ GFP+ or littermates were injected subcutaneously with MCA205 tumours and the tumour-infiltrating cells were harvested at day 14. (a) Dot plots show GFP expression in peripheral blood mononuclear cells (PBMC) or tumour-infiltrating cells from tumour-bearing OX40Cre+ GFP+ F1 mice or littermates. (b) CD4 and CD8 expression on gated GFP+ cells in the peripheral blood of a naive mouse or in a tumour. (c) GFP expression in gated d14 tumour-infiltrating CD4+ or CD11b+ cells from OX40Cre+ GFP+ or littermates. (d) Analysis of CD44 expression on gated CD8+ cells in the tumour-draining lymph node, non-draining lymph node and tumour of day 17 tumour-bearing OX40Cre+ GFP+ mice or littermates.