Ala-Laurila Petri, Cornwall M Carter, Crouch Rosalie K, Kono Masahiro
From the Department of Physiology and Biophysics, Boston University School of Medicine, Boston, Massachusetts 02118; Department of Biological and Environmental Sciences, University of Helsinki, Helsinki FI-00014, Finland.
From the Department of Physiology and Biophysics, Boston University School of Medicine, Boston, Massachusetts 02118.
J Biol Chem. 2009 Jun 12;284(24):16492-16500. doi: 10.1074/jbc.M109.004697. Epub 2009 Apr 22.
11-cis-retinol has previously been shown in physiological experiments to promote dark adaptation and recovery of photoresponsiveness of bleached salamander red cones but not of bleached salamander red rods. The purpose of this study was to evaluate the direct interaction of 11-cis-retinol with expressed human and salamander cone opsins, and to determine by microspectrophotometry pigment formation in isolated salamander photoreceptors. We show here in a cell-free system using incorporation of radioactive guanosine 5'-3-O-(thio)triphosphate into transducin as an index of activity, that 11-cis-retinol inactivates expressed salamander cone opsins, acting an inverse agonist. Similar results were obtained with expressed human red and green opsins. 11-cis-retinol had no significant effect on the activity of human blue cone opsin. In contrast, 11-cis-retinol activates the expressed salamander and human red rod opsins, acting as an agonist. Using microspectrophotometry of salamander cone photoreceptors before and after bleaching and following subsequent treatment with 11-cis-retinol, we show that 11-cis-retinol promotes pigment formation. Pigment was not formed in salamander red rods or green rods (containing the same opsin as blue cones) treated under the same conditions. These results demonstrate that 11-cis-retinol is not a useful substrate for rod photoreceptors although it is for cone photoreceptors. These data support the premise that rods and cones have mechanisms for handling retinoids and regenerating visual pigment that are specific to photoreceptor type. These mechanisms are critical to providing regenerated pigments in a time scale required for the function of these two types of photoreceptors.
11-顺式视黄醇先前在生理学实验中已表明可促进蝾螈红色视锥细胞漂白后的暗适应及光反应性恢复,但对蝾螈红色视杆细胞漂白后则无此作用。本研究的目的是评估11-顺式视黄醇与表达的人类及蝾螈视锥蛋白的直接相互作用,并通过显微分光光度法测定分离出的蝾螈光感受器中的色素形成。我们在此无细胞系统中表明,以放射性鸟苷5'-3-O-(硫代)三磷酸掺入转导蛋白作为活性指标,11-顺式视黄醇可使表达的蝾螈视锥蛋白失活,起反向激动剂的作用。对表达的人类红色和绿色视蛋白也获得了类似结果。11-顺式视黄醇对人类蓝色视锥蛋白的活性无显著影响。相反,11-顺式视黄醇可激活表达的蝾螈及人类红色视杆蛋白,起激动剂的作用。通过对蝾螈视锥光感受器漂白前后及随后用11-顺式视黄醇处理后的显微分光光度法检测,我们发现11-顺式视黄醇可促进色素形成。在相同条件下处理的蝾螈红色视杆细胞或绿色视杆细胞(含有与蓝色视锥相同的视蛋白)中未形成色素。这些结果表明,11-顺式视黄醇虽对视锥光感受器是有用的底物,但对视杆光感受器并非如此。这些数据支持这样的前提,即视杆细胞和视锥细胞具有处理类视黄醇及再生视色素的机制,这些机制是光感受器类型特异性的。这些机制对于在这两种类型光感受器功能所需的时间范围内提供再生色素至关重要。