Dawes J, Pumphrey C W, McLaren K M, Prowse C V, Pepper D S
Thromb Res. 1982 Jul 1;27(1):65-76. doi: 10.1016/0049-3848(82)90279-1.
Intravenous and subcutaneous injection of heparin or the heparin analogue SSHA into normal volunteers induced release of platelet factor 4 (PF4) but not beta-thromboglobulin (beta-TG). At low heparin doses the amount of PF4 released was related to the plasma heparin concentration achieved. The rise in plasma PF4 was coincident with, and appeared to be a response to, the increase in plasma heparin concentration rather than to the absolute heparin level. After the primary response, the system became refractory to further challenge by the same heparin dose; the full initial magnitude of the response was not regained until 144 h. after heparin was first injected. The maximum amount of PF4 released corresponded to only about 5% of that potentially available from platelets. Moreover, heparin did not stimulate PF4 release from whole blood in vitro. We have demonstrated the presence of PF4 on the vascular endothelium, and suggest that this is the immediate source of the PF4 released by heparin, though it is probably initially derived from platelets. The effect of such binding on the antithrombotic potential of the endothelial surface is discussed.
对正常志愿者静脉内和皮下注射肝素或肝素类似物SSHA可诱导血小板第4因子(PF4)释放,但不会诱导β-血小板球蛋白(β-TG)释放。在低剂量肝素时,释放的PF4量与达到的血浆肝素浓度相关。血浆PF4的升高与血浆肝素浓度的增加同时出现,并且似乎是对血浆肝素浓度增加的反应,而不是对绝对肝素水平的反应。初次反应后,该系统对相同肝素剂量的进一步刺激变得不应答;直到首次注射肝素后144小时才恢复到最初反应的完全强度。释放的PF4最大量仅相当于血小板中潜在可利用量的约5%。此外,肝素在体外不会刺激全血释放PF4。我们已经证明血管内皮细胞上存在PF4,并表明这是肝素释放的PF4的直接来源,尽管它最初可能源自血小板。讨论了这种结合对内皮表面抗血栓形成潜力的影响。