Bolsover S R, Brown J E
J Physiol. 1985 Jul;364:381-93. doi: 10.1113/jphysiol.1985.sp015751.
Photoreceptor cells of Limulus ventral eyes were bathed in artificial sea water (ASW) that contained 10 mM-EGTA and no added Ca2+ (EGTA-ASW). Test flashes elicited responses that increased to a maximum size within 10 min in EGTA-ASW but did not change further when dark-adapted cells were bathed for an additional 35 min in this solution. Light responses progressively declined from this maximum size if the cells were repetitively illuminated in EGTA-ASW. In this state of reduced responsiveness, response amplitudes were further reduced by intracellular ionophoretic injection of EGTA; response amplitudes were increased by intracellular ionophoretic injection of Ca2+. Both of these findings are opposite to what is normally observed for cells bathed in ASW. Also, after repetitive illumination in EGTA-ASW, both the slope of the response versus intensity relationship became steeper and light responses often had a delayed increase in amplitude. The light responses and the response versus intensity relation returned to normal when the bathing medium was changed back to ASW containing 10 mM-Ca2+. The light-induced rise in luminescence recorded from photoreceptors injected with the photoprotein aequorin (the 'aequorin response') declined by at most 50% after dark-adapted photoreceptors were bathed in EGTA-ASW for 45 min. However, the aequorin response progressively declined by 98% if cells were repetitively illuminated while bathed in EGTA-ASW. The total intracellular Ca content of whole end-organs was measured by atomic absorption spectroscopy. Total intracellular Ca content did not change significantly while photoreceptors were bathed in EGTA-ASW even after repetitive illumination. We suggest that cytosolic Ca2+ is required by one or more steps in the mechanisms that link rhodopsin isomerization to both (i) an increase in the conductance of the cell membrane to Na+ and (ii) a release of Ca2+ from a light-labile store.
鲎腹眼的光感受器细胞浸浴在含有10 mM乙二醇双乙醚二胺四乙酸(EGTA)且未添加Ca2+的人工海水(EGTA - ASW)中。测试闪光引发的反应在EGTA - ASW中10分钟内增加到最大幅度,但当暗适应细胞在此溶液中再浸浴35分钟时,反应不再进一步变化。如果细胞在EGTA - ASW中反复受到光照,光反应会从这个最大幅度逐渐下降。在这种反应性降低的状态下,通过细胞内离子电泳注射EGTA会进一步降低反应幅度;通过细胞内离子电泳注射Ca2+会增加反应幅度。这两个发现都与浸浴在ASW中的细胞通常观察到的情况相反。此外,在EGTA - ASW中反复光照后,反应与强度关系的斜率变得更陡,并且光反应的幅度通常会延迟增加。当浴液换回含有10 mM Ca2+的ASW时,光反应以及反应与强度的关系恢复正常。在用光蛋白水母发光蛋白注射的光感受器中记录到的光诱导发光增加(“水母发光蛋白反应”),在暗适应的光感受器浸浴在EGTA - ASW中45分钟后,最多下降50%。然而,如果细胞在浸浴在EGTA - ASW中时反复受到光照,水母发光蛋白反应会逐渐下降98%。通过原子吸收光谱法测量整个终末器官的细胞内总钙含量。即使在反复光照后,当光感受器浸浴在EGTA - ASW中时,细胞内总钙含量也没有显著变化。我们认为,在将视紫红质异构化与(i)细胞膜对Na+的电导增加以及(ii)从光不稳定储存库释放Ca2+相联系的机制中的一个或多个步骤需要胞质Ca2+。