Camussi G, Tetta C, Segoloni G, Chiara Deregibus M, Bussolino F
Agents Actions. 1981 Dec;11(6-7):550-3. doi: 10.1007/BF01978735.
Soluble and phagocytic stimuli released PAF-acether from PMN leucocytes, as determined by chromatography and bioassay by platelet aggregation. The same material caused aggregation of human and rabbit PMN leucocytes in vitro which was inhibited by ETYA and PGI2. PGI2 also inhibited PAF-acether release by PMN leucocytes and, in vivo, PGI2 abolished not only PAF-acether-induced, but also immune complex or C5a-induced thrombocytopenia and neutropenia in rabbits. These data suggest that PAF-acether may be involved in activation of both platelets and PMN leucocytes in vivo.
通过色谱法和血小板聚集生物测定法测定,可溶性和吞噬性刺激物可从多形核白细胞(PMN)中释放出血小板活化因子(PAF-乙醚)。相同物质在体外可导致人和兔PMN白细胞聚集,而这种聚集可被乙磺酰亚胺(ETYA)和前列环素(PGI2)抑制。PGI2还可抑制PMN白细胞释放PAF-乙醚,并且在体内,PGI2不仅可消除PAF-乙醚诱导的,还可消除免疫复合物或C5a诱导的兔血小板减少症和中性粒细胞减少症。这些数据表明,PAF-乙醚可能参与体内血小板和PMN白细胞的激活。