Table 1.
SAP IC50 values for the inhibition of fibrocyte differentiation in human and murine cell cultures.
| Cells | Mouse SAP IC50 μg/ml | Human SAP IC50 μg/ml |
|---|---|---|
| Human PBMC | 0.78 ± 0.15 | 0.41 ± 0.05* |
| Murine PBMC | 7.1 ± 1.0 | 1.6 ± 0.1** |
| Murine Spleen | 9.0 ± 2.1 | 1.3 ± 0.3** |
| Murine Spleen + Cytokines | 15 ± 3.7 | 1.9 ± 0.3** |
Human PBMCs, murine PBMCs, and murine spleen cells were cultured for 5 days at 5 × 104 cells per well, 2.5 × 105 cells per well, and 3.5 × 105 cells per well, respectively, in the presence of human and murine SAP. Murine spleen cells were also cultured in the presence or absence of the cytokines IL-13 and M-CSF. Cells were air dried, fixed, stained, and enumerated by morphology. Using fibrocyte counts normalized to SFM controls, IC50 levels were calculated by fitting SAP bioactivity to a sigmoidal dose response curve with variable slope. Results are expressed as mean ± SEM (n=5 for spleens, n=3 for mouse PBMCs, n=6 for human PBMCs). For the inhibition of fibrocyte differentiation by murine SAP, no significant difference was observed between the IC50 values for murine PBMCs and murine spleen cells (1-way ANOVA, Tukey’s test). Human SAP was significantly more effective than murine SAP on both human cells (p<0.05) and mouse cells (p<0.01; t-test).
p < 0.05;
p < 0.01.