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. 2010 Feb;77(2):159–170. doi: 10.1124/mol.109.060673

Fig. 2.

Fig. 2.

Analysis of Ca2+ mobilization in phagocytes treated with AG-09/1 and AG-09/4. HL-60-FPR1 and HL-60-FPR2 cells (A and B) or human neutrophils (C and D) were loaded with fluorometric imaging plate reader calcium 3 dye, and Ca2+ flux was analyzed, as described under Materials and Methods. Responses were normalized to the response induced by 5 nM fMLF for HL-60-FPR1 cells and neutrophils, or 5 nM WKYMVm for HL-60-FPRL1 cells, which were assigned a value of 100%. D, human neutrophils were treated with 5 μM concentrations of the compounds under investigation (AG-09/1 and AG-09/4), 5 nM fMLF (positive control), or 1% DMSO (negative control), and Ca2+ flux was monitored for the indicated times (arrow indicates when treatment was added). The data are from one experiment that is representative of three independent experiments.