Biró E, Akkerman J W N, Hoek F J, Gorter G, Pronk L M, Sturk A, Nieuwland R
Department of Clinical Chemistry, Academic Medical Center, University of Amsterdam, The Netherlands.
J Thromb Haemost. 2005 Dec;3(12):2754-63. doi: 10.1111/j.1538-7836.2005.01646.x.
The processes that govern the distribution of molecules between platelets and the microparticles (MP) they release are unknown. Certain proteins are sorted selectively into MP, but lipid sorting has not been studied.
To compare the phospholipid composition and cholesterol content of platelet-derived MP obtained with various stimuli with that of isolated platelet membrane fractions.
Washed platelets from venous blood of healthy individuals (n = 6) were stimulated with collagen, thrombin, collagen plus thrombin, or A23187. Platelet activation, MP release and antigen exposure were assessed by flow cytometry. MPs were isolated by differential centrifugation. Platelet plasma-, granule- and intracellular membranes were isolated from platelet concentrates (n = 3; 10 donors each) by pressure homogenization and Percoll density gradient fractionation. The phospholipid composition and cholesterol content of MPs and membrane fractions were analyzed by high performance thin layer chromatography.
The phospholipid composition of MPs was intermediate compared with that of platelet plasma- and granule membranes, and differed significantly from that of intracellular membranes. There were small but significant differences in phospholipid composition between the MPs produced by the various agonists, which paralleled differences in P-selectin exposure in case of the physiological agonists collagen, thrombin, or collagen plus thrombin. The cholesterol content of MPs tended to be higher than that of the three-platelet membrane fractions.
Regarding its phospholipid content, the MP membrane is a composite of the platelet plasma- and granule membranes, showing subtle differences depending on the platelet agonist. The higher cholesterol content of MPs suggests their enrichment in lipid rafts.
血小板与其释放的微粒(MP)之间分子分布的调控过程尚不清楚。某些蛋白质会被选择性地分选到MP中,但脂质分选尚未得到研究。
比较不同刺激条件下获得的血小板衍生MP与分离的血小板膜组分的磷脂组成和胆固醇含量。
用胶原蛋白、凝血酶、胶原蛋白加凝血酶或A23187刺激健康个体(n = 6)静脉血中的洗涤血小板。通过流式细胞术评估血小板活化、MP释放和抗原暴露情况。通过差速离心分离MP。通过压力匀浆和Percoll密度梯度分级从血小板浓缩物(n = 3;每个有10名供体)中分离血小板质膜、颗粒膜和内膜。通过高效薄层色谱分析MP和膜组分的磷脂组成和胆固醇含量。
与血小板质膜和颗粒膜相比,MP的磷脂组成处于中间水平,且与内膜有显著差异。不同激动剂产生的MP在磷脂组成上存在微小但显著的差异,这与生理激动剂胶原蛋白、凝血酶或胶原蛋白加凝血酶情况下P-选择素暴露的差异相似。MP的胆固醇含量往往高于三种血小板膜组分。
就磷脂含量而言,MP膜是血小板质膜和颗粒膜的复合物,根据血小板激动剂的不同表现出细微差异。MP较高的胆固醇含量表明它们在脂筏中富集。