Biernbaum M S, Bownds M D
J Gen Physiol. 1985 Jan;85(1):83-105. doi: 10.1085/jgp.85.1.83.
Purified suspensions of frog rod outer segments still attached to the mitochondria-rich inner segment portion of the receptor cell (OS-IS) can be obtained in quantities (0.1 mg/retina) sufficient for chemical analysis. In oxygenated glucose-bicarbonate Ringer's medium with added Percoll, they display normal dark currents, light sensitivity, and photocurrent kinetics for several hours. Two millimolar cytoplasmic levels of ATP and GTP are maintained, fivefold higher than in isolated OS. The levels are not altered by abolition of the dark current with ouabain. Nucleoside triphosphates are more effectively buffered than in isolated OS, and their levels remain constant during changes in external calcium levels. 32Pi is incorporated into endogenous ATP and GTP pools twice as efficiently as in isolated OS, and is used in the phosphorylation of rhodopsin. OS-IS take up and release 45Ca++ by Na+-, Ca++-, and IBMX-sensitive mechanisms. Illumination causes release of 45Ca++, which confirms retinal studies by other groups using Ca++-sensitive electrodes. Thus, OS-IS suspensions model the behavior of photoreceptors still attached to the living retina. Their availability permits the simultaneous assay and correlation of electrophysiological and chemical changes occurring during excitation and adaptation.
可以获得大量(0.1毫克/视网膜)仍附着于受体细胞富含线粒体的内段部分(视杆外段 - 内段,OS - IS)的青蛙视杆外段纯化悬浮液,足以进行化学分析。在添加了聚蔗糖的充氧葡萄糖 - 碳酸氢盐林格氏液中,它们在数小时内表现出正常的暗电流、光敏感度和光电流动力学。胞质中ATP和GTP的水平维持在2毫摩尔,比分离出的视杆外段高五倍。哇巴因消除暗电流并不会改变这些水平。核苷三磷酸的缓冲效果比分离出的视杆外段更有效,并且在外部钙水平变化期间其水平保持恒定。32Pi掺入内源性ATP和GTP池的效率是分离出的视杆外段的两倍,并用于视紫红质的磷酸化。视杆外段 - 内段通过对钠离子、钙离子和异丁基甲基黄嘌呤敏感的机制摄取和释放45Ca++。光照会导致45Ca++的释放,这证实了其他研究小组使用钙离子敏感电极进行的视网膜研究。因此视杆外段 - 内段悬浮液模拟了仍附着于活体视网膜的光感受器的行为。它们的可用性使得能够同时测定和关联兴奋和适应过程中发生的电生理和化学变化。