Oho C, Takisawa H
J Biochem. 1986 Oct;100(4):911-21. doi: 10.1093/oxfordjournals.jbchem.a121804.
The effects of phosphatidylinositol 4,5-bisphosphate (PtdInsP2) and inositol 1,4,5-triphosphate(InsP3) on the Ca2+ release from ATP-dependent Ca2+-transporting microsomes prepared from ox platelets were investigated. Under optimal conditions, both PtdInsP2 and InsP3 released Ca2+ from the microsomes in a similar dose-dependent manner. However, the maximal amount of Ca2+ released by InsP3 was almost one-fourth of that released by PtdInsP2. Neither PtdInsP2 nor InsP3 appeared to act as a Ca2+ ionophore since they showed no effect on the Ca2+ content of liposomes prepared from platelet microsomal lipids. InsP3-induced but not PtdInsP2-induced Ca2+ release was decreased with increasing extravesicular Ca2+ from 0.1 microM to 10 microM and it was completely inhibited by 10 microM Ca2+. PtdInsP2-induced but not InsP3-induced Ca2+ release was markedly inhibited by Mg2+, ruthenium red and neomycin. In addition, InsP3 could induce no additional Ca2+ release after the accumulated Ca2+ had been maximally released by PtdInsP2. These results indicate that PtdInsP2 releases Ca2+ from platelet microsomes more effectively than InsP3 by a mechanism distinct from that of InsP3-induced release, and further that InsP3-sensitive microsomes are included within the population of PtdInsP2-sensitive microsomes.
研究了磷脂酰肌醇4,5 - 二磷酸(PtdInsP2)和肌醇1,4,5 - 三磷酸(InsP3)对从牛血小板制备的依赖ATP的Ca2+转运微粒体释放Ca2+的影响。在最佳条件下,PtdInsP2和InsP3均以类似的剂量依赖性方式从微粒体中释放Ca2+。然而,InsP3释放的Ca2+最大量几乎是PtdInsP2释放量 的四分之一。PtdInsP2和InsP3似乎都不充当Ca2+离子载体,因为它们对由血小板微粒体脂质制备的脂质体的Ca2+含量没有影响。随着细胞外Ca2+从0.1微摩尔增加到10微摩尔,InsP3诱导的而非PtdInsP2诱导的Ca2+释放减少,并被10微摩尔Ca2+完全抑制。Mg2+、钌红和新霉素显著抑制PtdInsP2诱导的而非InsP3诱导的Ca2+释放。此外,在PtdInsP2将积累的Ca2+最大程度释放后,InsP3不能诱导额外的Ca2+释放。这些结果表明,PtdInsP2通过与InsP3诱导释放不同的机制比InsP3更有效地从血小板微粒体中释放Ca2+,并且进一步表明InsP3敏感的微粒体包含在PtdInsP2敏感的微粒体群体中。