Fig. 5.
Intracellular expression of cytokines in BM DCs at different stages of cell differentiation.
(A) Detection of intracellular cytokines by flow cytometry in CD86− and CD86+ BM DCs. CD11c+immunobead-sorted DCs were double labeled with FITC anti-CD86 and PE anticytokine mAbs. Figures within quadrants indicate percentages of cells. (B) Detection of TGF-β1 by ELISA in 24-hour culture supernatants of FACS-sorted CD86− DCs and CD86+ DCs (2 × 106 cells/well). Results are representative of 4 separate experiments.