Figure 3
Figure 3. IKK activity is important for platelet secretion. (A) Mouse platelets were prepared as described in our “Methods” section. After adding 0.7 mM CaCl2, platelets were incubated with (open symbols) or without (●) 5 μM BMS-345541 for 3 minutes, then stimulated with thrombin (0.05 U/mL) for the indicated times. (B) IKKβ−/− platelets (○) and platelets from Cre− littermate controls (●) were stimulated with thrombin (0.05 U/mL) under similar conditions. Release of [3H]5-HT from dense granules (Dense), PF4 from α-granules (Alpha), and β-hexosaminidase from lysosomes (Lysosome) was measured and percent secretion was calculated. Each data point represents the mean of triplicates and the standard deviation is indicated. (C) IKK-β+/+ and IKK-β−/− platelets were subjected to immunoblotting with anti-IKK-β antibody. (D) IKK-β+/+ and IKK-β−/− platelets were stimulated with 0.1 U/mL thrombin for 3 minutes and subjected to immunoblotting with anti-phospho-Ser95 (pSer-95) and anti-SNAP-23 antibodies.

IKK activity is important for platelet secretion. (A) Mouse platelets were prepared as described in our “Methods” section. After adding 0.7 mM CaCl2, platelets were incubated with (open symbols) or without (●) 5 μM BMS-345541 for 3 minutes, then stimulated with thrombin (0.05 U/mL) for the indicated times. (B) IKKβ−/− platelets (○) and platelets from Cre littermate controls (●) were stimulated with thrombin (0.05 U/mL) under similar conditions. Release of [3H]5-HT from dense granules (Dense), PF4 from α-granules (Alpha), and β-hexosaminidase from lysosomes (Lysosome) was measured and percent secretion was calculated. Each data point represents the mean of triplicates and the standard deviation is indicated. (C) IKK-β+/+ and IKK-β−/− platelets were subjected to immunoblotting with anti-IKK-β antibody. (D) IKK-β+/+ and IKK-β−/− platelets were stimulated with 0.1 U/mL thrombin for 3 minutes and subjected to immunoblotting with anti-phospho-Ser95 (pSer-95) and anti-SNAP-23 antibodies.

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