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Blood, Vol. 93 No. 10 (May 15), 1999:
pp. 3408-3417
Agonist-Induced Regulation of Myosin Phosphatase Activity in Human
Platelets Through Activation of Rho-Kinase
Yoshinori Suzuki,
Masatoshi Yamamoto,
Hideo Wada,
Masaaki Ito,
Takeshi Nakano,
Yasuharu Sasaki,
Shuh Narumiya,
Hiroshi Shiku, and
Masakatsu Nishikawa
From the 2nd and the 1st Departments of Internal Medicine, Mie
University School of Medicine, Tsu, Mie, Japan; Frontier 21, Life
Science Research Center, Asahi Chemical Industry Co, Ltd, Fuji,
Shizuoka; and the Department of Pharmacology, Kyoto University Faculty
of Medicine, Kyoto, Japan.
Human platelets contained about 15 times lower amounts of Rho-kinase
than Ca2+/calmodulin-dependent myosin light chain (MLC)
kinase. Anti-myosin-binding subunit (MBS) antibody
coimmunoprecipitated Rho-kinase of human platelets, and addition of
GTP S-RhoA stimulated phosphorylation of the 130-kD MBS of myosin
phosphatase and consequently inactivated myosin phosphatase. Two kinds
of selective Rho-kinase inhibitors, HA1077 and Y-27632, reduced both
GTP S-RhoA-dependent MBS phosphorylation and inactivation of the
phosphatase activity. Activation of human platelets with thrombin, a
stable thromboxane A2 analog STA2, epinephrine,
and serotonin resulted in an increase in MBS phosphorylation, and the
agonist-induced MBS phosphorylation was prevented by pretreatment with
the respective receptor antagonist. HA1077 and Y-27632 inhibited MBS
phosphorylation in platelets stimulated with these agonists. These
compounds also blocked agonist-induced inactivation of myosin phosphatase in intact platelets. In addition, HA1077 and Y-27632 inhibited 20-kD MLC phosphorylation at Ser19 and ATP
secretion of platelets stimulated with STA2, thrombin (0.05 U/mL), and simultaneous addition of serotonin and epinephrine, whereas
these compounds did not affect MLC phosphorylation or ATP secretion
when platelets were stimulated with more than 0.1 U/mL
thrombin. Thus, activation of Rho-kinase and the resultant phosphorylation of MBS is likely to be the common pathway for platelet
activation induced by various agonists. These results also suggest that
Rho-kinase-mediated MLC phosphorylation contributes to a greater
extent to the platelet secretion induced by relatively weak agonists.

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