Arribas I, Rodríguez-Puyol D, García-Escribano M C, Díez-Marques M L, Pérez de Lema G, Rodríguez-Puyol M
Clinical Chemistry Department University Hospital Príncipe de Asturias, Madrid, Spain.
Life Sci. 1995;57(10):957-65. doi: 10.1016/0024-3205(95)02030-m.
To analyze the metabolisms of platelet-activating factor (PAF) and Thromboxane A2 (TxA2) when platelets and mesangial cells (MC) interact, immunoreactive thromboxane B2 (TxB2) and PAF were measured after incubation of cultured rat MC with platelets (P) and with platelet supernatants (PS). In both cases, TxB2 significantly decreased with respect to the P synthesis and to the PS content, suggesting an increased degradation of this metabolite or even the existence of a specific effect of MC upon platelet TxB2. When immunoreactive PAF was measured, results were comparable to those observed for TxB2. Moreover, when intrinsic mesangial cell synthesis of PAF was assessed by analyzing the [3H]-acetate incorporation by prelabeled MC in the HPLC fraction coeluting with cold PAF standards, it was possible to demonstrate that P or PS did not modify PAF synthesis in these cells. In summary, present results support the existence of a specific effect of mesangial cells upon platelet TxA2 and PAF.
为分析血小板与系膜细胞(MC)相互作用时血小板活化因子(PAF)和血栓素A2(TxA2)的代谢情况,在培养的大鼠系膜细胞与血小板(P)及血小板上清液(PS)孵育后,检测免疫反应性血栓素B2(TxB2)和PAF。在这两种情况下,TxB2相对于P合成及PS含量均显著降低,提示该代谢产物降解增加,甚至存在系膜细胞对血小板TxB2的特异性作用。检测免疫反应性PAF时,结果与TxB2的观察结果相似。此外,通过分析预标记的系膜细胞中[3H] - 乙酸掺入与冷PAF标准品共洗脱的HPLC馏分来评估系膜细胞内源性PAF合成时,发现P或PS不会改变这些细胞中的PAF合成。总之,目前的结果支持系膜细胞对血小板TxA2和PAF存在特异性作用。