Fig. 1.
Fig. 1. Effect of inflammatory microcrystals on prostanoid synthesis by human monocytes. (A) Monocytes were incubated for 24 hours with either MSU or CPPD crystals at the indicated concentrations and cell-free supernatants were analyzed for prostanoid (PGE2and TXB2) synthesis. Data obtained from 3 donors are presented, and values are the mean ± SD of duplicate determinations. (B) Monocytes were incubated with MSU crystals (0.6 mg/mL) for the indicated times and prostanoid synthesis was measured. Data obtained from 3 donors are presented, and values are the mean ± SD of duplicate determinations. (C) Monocytes were stimulated in the absence (C), or presence of either MSU or CPPD crystals (0.6 mg/mL) for 24 hours and prostanoid synthesis was measured. When compared with control cells, MSU microcrystals induced significant prostanoid synthesis, *P < .01 (by t test). Data presented are the mean ± SD from at least seven experiments.

Effect of inflammatory microcrystals on prostanoid synthesis by human monocytes. (A) Monocytes were incubated for 24 hours with either MSU or CPPD crystals at the indicated concentrations and cell-free supernatants were analyzed for prostanoid (PGE2and TXB2) synthesis. Data obtained from 3 donors are presented, and values are the mean ± SD of duplicate determinations. (B) Monocytes were incubated with MSU crystals (0.6 mg/mL) for the indicated times and prostanoid synthesis was measured. Data obtained from 3 donors are presented, and values are the mean ± SD of duplicate determinations. (C) Monocytes were stimulated in the absence (C), or presence of either MSU or CPPD crystals (0.6 mg/mL) for 24 hours and prostanoid synthesis was measured. When compared with control cells, MSU microcrystals induced significant prostanoid synthesis, *P < .01 (by t test). Data presented are the mean ± SD from at least seven experiments.

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