Figure 4
Figure 4. Inhibition of calmodulin abrogates fMLP- and SDF-1–induced LDV-FITC binding. (A) U937-FPR cells were pretreated with DMSO or W7 and stimulated at time 0 with Mn2+, buffer, fMLP, or SDF-1. LDV-FITC binding was analyzed in real time. One of 3 independent experiments is shown. (B) Ionomycin-induced pH changes in BCECF-loaded U937-FPR cells were determined using a fluorometer. Cells were pretreated with DMSO, ethylisopropyl amiloride (EIPA; 10 μM), a Na+/H+ exchange inhibitor, or W7 and stimulated with ionomycin at time 0.

Inhibition of calmodulin abrogates fMLP- and SDF-1–induced LDV-FITC binding. (A) U937-FPR cells were pretreated with DMSO or W7 and stimulated at time 0 with Mn2+, buffer, fMLP, or SDF-1. LDV-FITC binding was analyzed in real time. One of 3 independent experiments is shown. (B) Ionomycin-induced pH changes in BCECF-loaded U937-FPR cells were determined using a fluorometer. Cells were pretreated with DMSO, ethylisopropyl amiloride (EIPA; 10 μM), a Na+/H+ exchange inhibitor, or W7 and stimulated with ionomycin at time 0.

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