Fig. 2.
Fig. 2. Typical traces showing the effect of PTX on intracellular Ca2+ transients induced by maximally effective concentrations of C5a, LTB4 , or PAF. Eosinophils were pretreated for 2.5 hours with vehicle (CN) or PTX (1 μg/mL, see the Materials and Methods). The cells were then labeled with fura-2-acetoxymethyl ester and washed and changes in fluorescence were monitored after activation with LTB4 (10−8 mol/L), C5a (10−7 mol/L), or PAF (10−8 mol/L). The time of the addition of the agonists is shown by the arrows. Results are expressed as the increase in the concentration of intracellular calcium (in nanomoles per liter) as a function of time (in seconds).

Typical traces showing the effect of PTX on intracellular Ca2+ transients induced by maximally effective concentrations of C5a, LTB4 , or PAF. Eosinophils were pretreated for 2.5 hours with vehicle (CN) or PTX (1 μg/mL, see the Materials and Methods). The cells were then labeled with fura-2-acetoxymethyl ester and washed and changes in fluorescence were monitored after activation with LTB4 (10−8 mol/L), C5a (10−7 mol/L), or PAF (10−8 mol/L). The time of the addition of the agonists is shown by the arrows. Results are expressed as the increase in the concentration of intracellular calcium (in nanomoles per liter) as a function of time (in seconds).

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