Figure 3.
Figure 3. Cytokine production by DCs, Mø1s, and Mø2s after LPS stimulation or uptake of apoptotic cells. (A-C) Day-6 DCs, Mø1s, and Mø2s were extensively washed, and subsequently stimulated with or without LPS for 24 hours. (D-F) DCs, Mø1s, or Mø2s (1 × 105 cells) were cocultured with etoposide-induced apoptotic cells at a 1:1 ratio for 24 hours in RPMI culture medium. Supernatants were harvested and measured by ELISA for IL-10, IL-6, and TNF-α. Data are presented as mean ± SD from duplicate cultures and are representative of at least 3 independent experiments where cells are generated from separate unrelated donors. Dashed lines represent the detection limits of ELISA.

Cytokine production by DCs, Mø1s, and Mø2s after LPS stimulation or uptake of apoptotic cells. (A-C) Day-6 DCs, Mø1s, and Mø2s were extensively washed, and subsequently stimulated with or without LPS for 24 hours. (D-F) DCs, Mø1s, or Mø2s (1 × 105 cells) were cocultured with etoposide-induced apoptotic cells at a 1:1 ratio for 24 hours in RPMI culture medium. Supernatants were harvested and measured by ELISA for IL-10, IL-6, and TNF-α. Data are presented as mean ± SD from duplicate cultures and are representative of at least 3 independent experiments where cells are generated from separate unrelated donors. Dashed lines represent the detection limits of ELISA.

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