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. Author manuscript; available in PMC: 2015 Mar 16.
Published in final edited form as: J Immunol. 2011 Dec 2;188(1):294–301. doi: 10.4049/jimmunol.1101590

Figure 3.

Figure 3

The immunosuppressive function of Gr1+CD11b+ cells is nitric oxide and cell contact dependent. A) T cells were cultured as described in Materials and Methods. The addition of the pan-nitric oxide synthase inhibitor L-NAME (1mM) reversed the suppression of both CD4+ and CD8+ T cell proliferation by Gr1+CD11b+ cells; B) The presence of a transwell abrogated the suppression of T cells by Gr1+CD11b+ cells. CD4+ and CD8+ T cells were co-cultured with purified Gr1+CD11b+ cells in the presence or absence of transwell as described in Materials and Methods. Three independent experiments were performed and one representative data set is shown. *p<0.05, **p<0.001, ***p<0.0001.

The background CPM counts were between 300–800.