Background-Cholesterol 3-sulfate is present on a variety of cells and in hu
man LP)LI and it has been found in atherosclerotic lesions of human aorta.
Its precise biological role has not yet been described.
Methods and Results-In this study, eve investigated the interaction of plat
elets with cholesterol sulfate, Platelets adhered in a concentration-depend
ent and saturable manner to cholesterol sulfate but did not adhere to chole
sterol cholesterol acetate, estrone sulfate, or dehydroepiandrosterone sulf
ate, suggesting that the specificity of this interaction is determined not
only by the cholesterol moiety but also by the sulfate group, This adhesion
did not increase after platelet activation, and it was not cation-dependen
t, Soluble cholesterol sulfate inhibited adhesion in a concentration-depend
ent manner. However, antibodies against glycoprotein Ib glycoprotein IIb/lI
Ia, CD36, P-selectin, von Willebrand factor, or thrombospondin had no signi
ficant effect on platelet adhesion to cholesterol sulfate, Perfusion of who
le blood in a parallel-plate flow chamber resulted in the rapid and progres
sive adhesion of platelets to cholesterol sulfate but not to cholesterol ac
etate or estrone sulfate.
Conclusions-Cholesterol sulfate supports platelet adhesion and may be one o
f the factors determining the prothrombotic potential of atherosclerotic le
sions.