Smith J B, Smith L, Higgins B L
J Biol Chem. 1985 Nov 25;260(27):14413-6.
Inositol 1,4,5-trisphosphate (IP3) rapidly increased 45Ca2+ efflux from a nonmitochondrial organelle in cultured vascular smooth muscle cells that were permeabilized with saponin. A nucleotide, preferably ATP, was essential for IP3-evoked 45Ca2+ release. Two nonhydrolyzable ATP analogues satisfied the nucleotide requirement for IP3-evoked 45Ca2+ release. IP3 strongly stimulated 45Ca2+ efflux at low temperatures (1 to 15 degrees C). Decreasing the temperature from 37 to 4 degrees C inhibited the rate of IP3-stimulated efflux by only about 33%. The failure of such low temperatures to strongly inhibit IP3-induced 45Ca2+ efflux suggests that IP3 activated a Ca2+ channel, rather than a carrier, by a ligand-binding, rather than a metabolic, reaction.
肌醇1,4,5-三磷酸(IP3)可迅速增加经皂角苷通透处理的培养血管平滑肌细胞中非线粒体细胞器的45Ca2+外流。一种核苷酸,最好是ATP,对于IP3引发的45Ca2+释放至关重要。两种不可水解的ATP类似物满足了IP3引发的45Ca2+释放对核苷酸的需求。IP3在低温(1至15摄氏度)下强烈刺激45Ca2+外流。将温度从37摄氏度降至4摄氏度仅使IP3刺激的外流速率降低约33%。如此低温未能强烈抑制IP3诱导的45Ca2+外流,这表明IP3通过配体结合而非代谢反应激活了Ca2+通道,而非载体。