Figure 2
Figure 2. PGE1 inhibits Ca2+ and RhoA/ROCK-dependent phosphorylation of MLC. Washed platelets (3 × 108 platelets per milliliter) were stimulated with thrombin (0.05 U/mL) for 1 minute in the presence or absence of Y27632 (10 µM), BAPTA-AM (20 µM), or PGE1 (100 nM), and phospho-MLCser19 was assessed by immunoblotting. (A) Representative immunoblots from 5 independent experiments. (B) Densitometry of MLCser19 phosphorylation of 5 different experiments. ns, not significant. *P < .05 compared with thrombin only; **P < .01 compared with thrombin only.

PGE1 inhibits Ca2+ and RhoA/ROCK-dependent phosphorylation of MLC. Washed platelets (3 × 108 platelets per milliliter) were stimulated with thrombin (0.05 U/mL) for 1 minute in the presence or absence of Y27632 (10 µM), BAPTA-AM (20 µM), or PGE1 (100 nM), and phospho-MLCser19 was assessed by immunoblotting. (A) Representative immunoblots from 5 independent experiments. (B) Densitometry of MLCser19 phosphorylation of 5 different experiments. ns, not significant. *P < .05 compared with thrombin only; **P < .01 compared with thrombin only.

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