Dainaka J, Ichikawa A, Koibuchi Y, Nakagawa M, Tomita K
Biochem Pharmacol. 1986 Nov 1;35(21):3739-44. doi: 10.1016/0006-2952(86)90659-3.
When the tridecamer component of compound 48/80 (Fraction D, Fr.D), a Ca2+-dependent histamine releaser, was incubated with rat mast cells that had been prelabeled with [32P]phosphate, [3H]inositol or [3H]glycerol, it induced a rapid decrease in [32P]phosphatidylinositol-4,5-bisphosphate (PIP2) followed by increases of [3H]inositol-1,4,5-trisphosphate (Ins P3) and [3H]diacylglycerol during the 10 sec prior to detectable histamine release. Fr.D-induced changes of the metabolism of these compounds occurred even in the absence of Ca2+, but to a lesser extent than in the presence of Ca2+. In contrast, the accumulation of [3H]arachidonic acid into phosphatidylcholine (PC), phosphatidylinositol (PI) and phosphatidic acid (PA) in [3H]arachidonic acid-prelabeled mast cells was Ca2+-dependently stimulated by Fr.D with a concomitant decrease in [3H]phosphatidylethanolamine (PE). These Ca2+-dependent changes in PC and PE were not observed in mast cells preloaded with [32P]phosphate, while [32P]PI and [32P]PA increased Ca2+ independently. Fr.D also increased 45Ca2+ uptake by mast cells within 5 sec after the stimulation. These results indicate that Fr.D binding to mast cell Ca2+ independently induces rapid changes of PI cycle-related metabolism of plasma membrane components, while it also induces Ca2+-dependent accumulation of arachidonic acid into PC, PI and PA in association with the decrease of PE, which may be important during the latent period prior to the Ca2+-dependent release of histamine from Fr.D-stimulated mast cells.
化合物48/80的十三聚体成分(D组分,Fr.D)是一种依赖Ca2+的组胺释放剂,当它与预先用[32P]磷酸盐、[3H]肌醇或[3H]甘油标记的大鼠肥大细胞一起孵育时,在可检测到组胺释放前的10秒内,它会导致[32P]磷脂酰肌醇-4,5-二磷酸(PIP2)迅速减少,随后[3H]肌醇-1,4,5-三磷酸(Ins P3)和[3H]二酰基甘油增加。即使在没有Ca2+的情况下,Fr.D也会引起这些化合物代谢的变化,但程度比有Ca2+时小。相反,在[3H]花生四烯酸预先标记的肥大细胞中,Fr.D以Ca2+依赖的方式刺激[3H]花生四烯酸积累到磷脂酰胆碱(PC)、磷脂酰肌醇(PI)和磷脂酸(PA)中,同时[3H]磷脂酰乙醇胺(PE)减少。在用[32P]磷酸盐预加载的肥大细胞中未观察到PC和PE的这些Ca2+依赖性变化,而[32P]PI和[32P]PA则独立于Ca2+增加。Fr.D还在刺激后5秒内增加了肥大细胞对45Ca2+的摄取。这些结果表明,Fr.D与肥大细胞Ca2+结合可独立诱导质膜成分中PI循环相关代谢的快速变化,同时它还诱导Ca2+依赖的花生四烯酸积累到PC、PI和PA中,并伴有PE的减少,这在Fr.D刺激的肥大细胞Ca2+依赖的组胺释放潜伏期可能很重要。