Thrombin-induced activation of RhoA and its involvement in the regulation o
f myosin II light chain(20) phosphorylation (MLC-P) in alpha -toxin permeab
ilized platelets was investigated. Permeabilized platelets, expressing norm
al levels of P-selectin, displayed a Ca2+-dependent increase in shape chang
e and MLC-P. Thrombin activated RhoA as measured by a rhotekin-binding assa
y within 30 s of stimulation under conditions of constant [Ca2+](i). Under
the same conditions and timecourse, thrombin or GTP gammaS induced an incre
ase in MLC-P and platelet shape change which was not dependent on an increa
se in [Ca2+](i). The thrombin- and GTP gammaS-induced MLC-P in constant [Ca
2+](i) was inhibited by the addition of Y27632, a Rho-kinase inhibitor. Thi
s study directly demonstrates that thrombin can activate RhoA in platelets
in a timecourse compatible with a role in increasing MLC-P and shape change
(not involving an increase in [Ca2+](i)). This is also Rho-kinase-dependen
t. (C) 2001 Academic Press.