Authi K S, Crawford N
Biochem J. 1985 Aug 15;230(1):247-53. doi: 10.1042/bj2300247.
Evidence has accumulated in support of a role for intracellularly generated inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] in raising cytosol [Ca2+] when various hormones, neurotransmitters, growth factors and other stimulants act on cell surfaces. The increase in [Ca2+] that follows stimulant-receptor interaction is accompanied by rapid hydrolysis of phosphoinositides. One product, Ins(1,4,5)P3, arising from the breakdown of phosphatidylinositol 4,5-bisphosphate was shown to promote the release of Ca2+ from non-mitochondrial stores in a variety of cells. Although platelet intracellular membranes have been implicated in the control of cytosol [Ca2+] and we previously characterized a Ca2+-sequestering mechanism associated with them, we have as yet no knowledge of how this Ca2+ store is mobilized after a stimulus-receptor interaction at the platelet surface. Using free-flow electrophoresis, we isolated and purified human platelet intracellular membranes. They show high enrichment and exclusive localization of the endoplasmic-reticulum marker NADH:cytochrome c reductase, and they sequester Ca2+ by an ATP-dependent process, reaching steady-state values in 10-12 min. Saturation with Ca2+ occurs at around 10-30 microM external Ca2+. When Ins(1,4,5)P3 is added to the 45Ca-loaded vesicles, a rapid release of Ca2+ occurs (approx. 35% in 15-30s). The magnitude of the release depends upon external [Ca2+], being maximum in the range 0.3-0.8 microM and low at external [Ca2+] greater than 1 microM. After release there is a rapid re-uptake of Ca2+, with restoration of the former steady-state values within 1 min. Half-maximal release occurs at approx. 0.25 microM-Ins(1,4,5)P3. This release and re-uptake pattern is not observed with ionophore A23187 or arachidonic acid, both of which liberate Ca2+ irreversibly. Inositol 1,4-bisphosphate was ineffective in releasing Ca2+ from these intracellular membranes. The results support the role of Ins(1,4,5)P3 as a specific intracellular mediator, transducing the action of excitatory agonists acting on the platelet surface into metabolic, mechanochemical and other functional events, known to occur during platelet activation.
有证据表明,当各种激素、神经递质、生长因子和其他刺激物作用于细胞表面时,细胞内生成的肌醇1,4,5-三磷酸[Ins(1,4,5)P3]在升高胞质溶胶[Ca2+]方面发挥作用。刺激物与受体相互作用后[Ca2+]的增加伴随着磷酸肌醇的快速水解。一种产物,即由磷脂酰肌醇4,5-二磷酸分解产生的Ins(1,4,5)P3,已被证明能促进多种细胞中非线粒体钙库释放Ca2+。尽管血小板细胞内膜与胞质溶胶[Ca2+]的调控有关,且我们之前已对与其相关的Ca2+螯合机制进行了表征,但我们尚不清楚在血小板表面发生刺激物与受体相互作用后,该Ca2+库是如何被动员的。我们使用自由流动电泳分离并纯化了人血小板细胞内膜。它们显示出内质网标记物NADH:细胞色素c还原酶的高度富集和专属定位,并且它们通过依赖ATP的过程螯合Ca2+,在10 - 12分钟内达到稳态值。在外部Ca2+浓度约为10 - 30 microM时发生Ca2+饱和。当将Ins(1,4,5)P3添加到负载45Ca的囊泡中时,会迅速释放Ca2+(在15 - 30秒内约释放35%)。释放的幅度取决于外部[Ca2+],在0.3 - 0.8 microM范围内最大,在外部[Ca2+]大于1 microM时较低。释放后Ca2+会迅速重新摄取,在1分钟内恢复到先前的稳态值。半最大释放发生在约0.25 microM - Ins(1,4,5)P3时。用离子载体A23187或花生四烯酸未观察到这种释放和重新摄取模式,这两种物质都会不可逆地释放Ca2+。肌醇1,4-二磷酸在从这些细胞内膜释放Ca2+方面无效。这些结果支持Ins(1,4,5)P3作为一种特定的细胞内介质的作用,将作用于血小板表面的兴奋性激动剂的作用转化为代谢、机械化学和其他功能事件,这些事件已知在血小板激活过程中发生。