Fig. 7.
Fig. 7. IP3 production and calcium release are not observed in platelets stimulated with vWF plus botrocetin. / (A) IP3: after human platelets were stimulated with 75 μg/mL collagen (▪) or 6 μg/mL botrocetin plus 10 μg/mL vWF (▧) for the indicated time periods, the production of IP3was measured as described in “Materials and methods.” The data are expressed as means ± SEM of 3 separate experiments. (B) Ca++: stimulation of human platelets with 75 μg/mL collagen (i) or 6 μg/mL botrocetin plus 10 μg/mL vWF (ii) was initiated at the time indicated by the arrow. The [Ca++]i elevation in the absence of extracellular calcium was monitored as changes in fura2 fluorescence for 300 seconds. The ordinate represents the ratio of fura2 fluorescence. The results are representative of 3 experiments.

IP3 production and calcium release are not observed in platelets stimulated with vWF plus botrocetin.

(A) IP3: after human platelets were stimulated with 75 μg/mL collagen (▪) or 6 μg/mL botrocetin plus 10 μg/mL vWF (▧) for the indicated time periods, the production of IP3was measured as described in “Materials and methods.” The data are expressed as means ± SEM of 3 separate experiments. (B) Ca++: stimulation of human platelets with 75 μg/mL collagen (i) or 6 μg/mL botrocetin plus 10 μg/mL vWF (ii) was initiated at the time indicated by the arrow. The [Ca++]i elevation in the absence of extracellular calcium was monitored as changes in fura2 fluorescence for 300 seconds. The ordinate represents the ratio of fura2 fluorescence. The results are representative of 3 experiments.

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