Levine S P, Moake J L
Thromb Res. 1984 Nov 1;36(3):233-43. doi: 10.1016/0049-3848(84)90223-8.
Ristocetin, protamine and Polybrene promote factor VIII:vWF binding and agglutination of formalinized platelets. It has been suggested that these polycations neutralize platelet negative surface charges and promote the attachment of VIII:vWF to platelets. Platelet factor 4 (PF4), protamine, and Polybrene inhibit heparin activity by neutralizing heparin negative charges. We tested the hypothesis that PF4, which is bound to the platelet surface after platelet activation and secretion, could promote the binding of VIII:vWF and subsequent platelet agglutination. Purified PF4 in concentrations comparable to those of ristocetin did not agglutinate formalinized platelets or induce the disappearance of VIII:vWF from the suspending plasma. Platelets were thrombin-treated in order to induce the release of PF4, and then formalinized and resuspended in normal plasma. These platelets did not agglutinate spontaneously, or at lower ristocetin concentrations than platelets that were not treated with thrombin before formalin fixation. Platelets were also activated by thrombin in the presence of EDTA to prevent surface binding of VIII:vWF or secreted PF4, and then formalinized. These platelets did not bind VIII:vWF in the presence of purified PF4. We conclude that even though PF4 binds to both polyanions and the platelet membrane, it does not promote the attachment of VIII:vWF.
瑞斯托霉素、鱼精蛋白和聚凝胺可促进因子VIII:血管性血友病因子(vWF)结合以及甲醛固定血小板的凝集。有人提出,这些聚阳离子可中和血小板表面的负电荷,并促进VIII:vWF与血小板的附着。血小板第4因子(PF4)、鱼精蛋白和聚凝胺通过中和肝素的负电荷来抑制肝素活性。我们检验了这样一个假说,即血小板活化和分泌后与血小板表面结合的PF4可促进VIII:vWF的结合及随后的血小板凝集。浓度与瑞斯托霉素相当的纯化PF4不会使甲醛固定的血小板凝集,也不会导致悬浮血浆中VIII:vWF消失。对血小板进行凝血酶处理以诱导PF4释放,然后进行甲醛固定并重新悬浮于正常血浆中。这些血小板不会自发凝集,在瑞斯托霉素浓度低于甲醛固定前未用凝血酶处理的血小板时也不会凝集。血小板还在乙二胺四乙酸(EDTA)存在的情况下用凝血酶激活,以防止VIII:vWF或分泌的PF4与表面结合,然后进行甲醛固定。在纯化PF4存在的情况下,这些血小板不会结合VIII:vWF。我们得出结论,尽管PF4可与多阴离子和血小板膜结合,但它不会促进VIII:vWF的附着。