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. 2005 Apr;114(4):499–506. doi: 10.1111/j.1365-2567.2005.02118.x

Figure 3.

Figure 3

Nitric oxide (NO) and transforming growth factor-β1 (TGF-β1) production by immature dendritic cells (iDCs) and mature DCs (mDCs) from interleukin (IL)-12/IL-23−/− and C57BL/6 mice. Bone marrow-derived DCs were cultured in the absence (iDCs) or presence (mDCs) of lipopolysaccharide (LPS) (1 µg/ml) for 18 hr. After washing, the cells (106) were incubated for a further 48 hr, with or without recombinant interferon-γ (rIFN-γ) (2·5 ng/ml).(a)NO was quantified in culture supernatants by using the Griess reaction. The experiments were repeated four times, with the same pattern of results obtained on each occasion.(b)TGF-β1 was quantified in culture supernatants by enzyme-linked immunosorbent assay (ELISA). The experiments were repeated twice, with the same pattern of results obtained on each occasion. Data represent the mean values ± standard deviation (SD) of a representative experiment. SD values were calculated from triplicate samples. *P < 0·05 versus C57BL/6 DCs.