Figure 4.
Figure 4. IgE, but not SF, requires the entry of extracellular calcium to trigger BMMC adhesion to FN. (A) Adhesion of normal BMMCs to FN in response to medium alone (C), 1 μg/mL IgE, or 5 ng/mL SF for 30 minutes with (□) or without (▪) the addition of 1.8 mM CaCl2. (B) Intracellular calcium measurements in BMMCs stimulated with 5 μg/mL IgE (thin solid line; left panel) or 50 ng/mL SF (thin solid line; right panel) alone, or in the presence of 50 μM 2-APB (dashed line) or 5 mM EGTA (thick solid line). The 2-APB was pre-incubated with the cells for 30 minutes, whereas the EGTA was added immediately prior to the addition of IgE or SF at 100 seconds (↓). (C) Adhesion of BMMCs to FN in response to 1 μg/mL IgE or 5 ng/mL SF for 30 minutes in the presence of vehicle control (□), 25 μM (▪), or 50 μM (▨) 2-APB added 30 minutes prior to stimulation. The background adhesion (6%) was subtracted. Adhesion was significantly (P < .05) different between IgE- and IgE + 2-APB–stimulated, but not SF- and SF + 2-APB–stimulated samples. Results shown are the mean ± SEM of triplicate determinations. Similar results were obtained in 3 (A), 3 (B), and 3 (C) separate experiments.

IgE, but not SF, requires the entry of extracellular calcium to trigger BMMC adhesion to FN. (A) Adhesion of normal BMMCs to FN in response to medium alone (C), 1 μg/mL IgE, or 5 ng/mL SF for 30 minutes with (□) or without (▪) the addition of 1.8 mM CaCl2. (B) Intracellular calcium measurements in BMMCs stimulated with 5 μg/mL IgE (thin solid line; left panel) or 50 ng/mL SF (thin solid line; right panel) alone, or in the presence of 50 μM 2-APB (dashed line) or 5 mM EGTA (thick solid line). The 2-APB was pre-incubated with the cells for 30 minutes, whereas the EGTA was added immediately prior to the addition of IgE or SF at 100 seconds (↓). (C) Adhesion of BMMCs to FN in response to 1 μg/mL IgE or 5 ng/mL SF for 30 minutes in the presence of vehicle control (□), 25 μM (▪), or 50 μM (▨) 2-APB added 30 minutes prior to stimulation. The background adhesion (6%) was subtracted. Adhesion was significantly (P < .05) different between IgE- and IgE + 2-APB–stimulated, but not SF- and SF + 2-APB–stimulated samples. Results shown are the mean ± SEM of triplicate determinations. Similar results were obtained in 3 (A), 3 (B), and 3 (C) separate experiments.

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