Figure 4.
Figure 4. Effect of PGE2 on exocytosis of β-hex by hMCs. (A) hMCs were primed for 5 days with IL-4, sensitized with IgE overnight, and then stimulated with medium alone, anti-IgE, or staphylococcal PGN (50 μg/mL) for 30 minutes in the presence or absence of PGE2 (10 μM). Values are expressed as percent of total cellular β-hex release and are the mean ± SEM from 5 experiments. (B) Primed and unprimed hMCs were stimulated for 30 minutes with PGE2 (10 μM) and compared for exocytosis. Some of the primed cells were treated overnight with PTX before activation. Values are mean ± SEM from 3 experiments. *Significant relative to unprimed cells.

Effect of PGE2 on exocytosis of β-hex by hMCs. (A) hMCs were primed for 5 days with IL-4, sensitized with IgE overnight, and then stimulated with medium alone, anti-IgE, or staphylococcal PGN (50 μg/mL) for 30 minutes in the presence or absence of PGE2 (10 μM). Values are expressed as percent of total cellular β-hex release and are the mean ± SEM from 5 experiments. (B) Primed and unprimed hMCs were stimulated for 30 minutes with PGE2 (10 μM) and compared for exocytosis. Some of the primed cells were treated overnight with PTX before activation. Values are mean ± SEM from 3 experiments. *Significant relative to unprimed cells.

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