Nofer J R, Walter M, Kehrel B, Seedorf U, Assmann G
Institut für Klinische Chemie und Laboratoriumsmedizin, Westfälische Wilhelms-Universität Münster, Germany.
Biochem Biophys Res Commun. 1995 Feb 6;207(1):148-54. doi: 10.1006/bbrc.1995.1165.
Glycoprotein IIb/IIIa has been proposed as the platelet receptor for high density lipoproteins (HDL3). We characterized the HDL3-induced second messenger response in normal and glycoprotein IIb/IIIa-deficient platelets. In normal platelets physiological concentrations of HDL3 induced the time-dependent generation of phosphatidic acid in the absence of phosphoinositide turnover. The rise in phosphatidic acid preceded that of diacyglycerol which was inconsistent with phospholipase C/diacylglycerol kinase pathway being the source of phosphatidic acid and suggested the involvement of phospholipase D. In the presence of butanol, HDL3 stimulated the accumulation of phosphatidylbutanol, an unequivocal indicator of phospholipase D activity. No increase in phosphatidic acid, diacylglycerol, and phosphatidylbutanol was observed upon addition of HDL3 to glycoprotein IIb/IIIa-deficient platelets. We conclude that phosphatidic acid is generated in HDL3-stimulated platelets by phospholipase D and that glycoprotein IIb/IIIa is the receptor involved in this process.
糖蛋白IIb/IIIa已被提出作为高密度脂蛋白(HDL3)的血小板受体。我们对正常血小板和缺乏糖蛋白IIb/IIIa的血小板中HDL3诱导的第二信使反应进行了表征。在正常血小板中,生理浓度的HDL3在不存在磷酸肌醇周转的情况下诱导了磷脂酸的时间依赖性生成。磷脂酸的升高先于二酰基甘油,这与磷脂酶C/二酰基甘油激酶途径作为磷脂酸来源不一致,并提示磷脂酶D参与其中。在丁醇存在的情况下,HDL3刺激了磷脂酰丁醇的积累,这是磷脂酶D活性的明确指标。将HDL3添加到缺乏糖蛋白IIb/IIIa的血小板中后,未观察到磷脂酸、二酰基甘油和磷脂酰丁醇的增加。我们得出结论,磷脂酸是由磷脂酶D在HDL3刺激的血小板中产生的,并且糖蛋白IIb/IIIa是参与此过程的受体。