Figure 5
GM-CSF regulates CD4
+ effector T cells through MFG-E8.
(A) Peritoneal macrophages were exposed to apoptotic thymocytes and cocultured with syngeneic wild-type CD3+CD45RA+CD62hi naive T cells. T cells were then analyzed for IL-17 and IFN-γ production. Numbers refer to the percentage of cells within an indicated gate. (B) Flt3-L–derived bone marrow dendritic cells were exposed to apoptotic thymocytes and used to stimulate syngeneic wild-type naive T cells. (C) Engineered macrophages were exposed to apoptotic thymocytes and used to stimulate syngeneic wild-type naive T cells. (D). Splenocytes were stimulated with PMA and ionomycin, and cytokine production of gated CD3+CD4+ cells was determined by flow cytometry. Similar results were obtained in at least 2 experiments.