König B, Bergmann U, König W
Lehrstuhl für Medizinische Mikrobiologie und Immunologie, Ruhr-Universität Bochum, Germany.
Infect Immun. 1992 Aug;60(8):3150-5. doi: 10.1128/iai.60.8.3150-3155.1992.
Purified glycolipid from Pseudomonas aeruginosa induced the generation of significant amounts of 12-hydroxyeicosatetraenoic acid (12-HETE) and serotonin release from human platelets. The release of serotonin was first observed 2 min after addition of the glycolipid and increased with time. Significant serotonin release was obtained at glycolipid concentrations above 5 micrograms/ml and increased dose-dependently up to 100% at glycolipid concentrations above 40 micrograms/ml. Glycolipid induced 12-HETE in a time- and dose-dependent manner. 12-HETE formation was first measured after 10 min of incubation and increased with time. Optimal 12-HETE formation was obtained at a glycolipid concentration of 50 micrograms/ml; higher concentrations of glycolipid led to a decrease in 12-HETE formation, indicating a cytotoxic effect. Stimulation of platelets with glycolipid (12-HETE formation and serotonin release) was accompanied by calcium influx, translocation of protein kinase C, activation of guanylylimidodiphosphate binding, and increased GTPase activity in platelet membranes within the same concentration range.
从铜绿假单胞菌中纯化的糖脂可诱导人血小板产生大量的12-羟基二十碳四烯酸(12-HETE)并释放5-羟色胺。在加入糖脂后2分钟首次观察到5-羟色胺的释放,且随时间增加。当糖脂浓度高于5微克/毫升时可获得显著的5-羟色胺释放,在糖脂浓度高于40微克/毫升时,其释放呈剂量依赖性增加,最高可达100%。糖脂以时间和剂量依赖性方式诱导12-HETE的产生。在孵育10分钟后首次检测到12-HETE的形成,并随时间增加。在糖脂浓度为50微克/毫升时可获得最佳的12-HETE形成;更高浓度的糖脂会导致12-HETE形成减少,表明具有细胞毒性作用。在相同浓度范围内,用糖脂刺激血小板(12-HETE形成和5-羟色胺释放)伴随着钙内流、蛋白激酶C易位、鸟苷酰亚胺二磷酸结合激活以及血小板膜中GTP酶活性增加。