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鼠眼视杆细胞漂白:显微分光光度法和抽吸电极记录

Bleaching of mouse rods: microspectrophotometry and suction-electrode recording.

机构信息

Department of Physiology and Biophysics, Boston University School of Medicine, Boston, MA 02118-2526, USA.

出版信息

J Physiol. 2012 May 15;590(10):2353-64. doi: 10.1113/jphysiol.2012.228627. Epub 2012 Mar 25.

Abstract

When a substantial fraction of rhodopsin in a rod photoreceptor is exposed to bright light, the rod is desensitized by a process known as bleaching adaptation. Experiments on isolated photoreceptors in amphibians have revealed many of the features of bleaching adaptation, but such experiments have not so far been possible in mammals. We now describe a method for making microspectrophotometric measurements of pigment concentration and suction-electrode recording of electrical responses over a wide range of bleaching exposures from isolated mouse rods or pieces of mouse retina. We show that if pigment is bleached at a low rate in the presence of bovine serum albumin (BSA), and intermediate photoproducts are allowed to decay, mouse rods are stably desensitized; subsequent treatment with exogenous 11-cis retinal results in pigment regeneration and substantial recovery of sensitivity to the dark-adapted value. Stably bleached wild-type (WT) rods show a decrease in circulating current and acceleration of the time course of decay, much as in steady background light; similar effects are seen in guanylyl cyclase-activating protein knockout (GCAPs(-/-)) rods, indicating that regulation of guanylyl cyclase is not necessary for at least a part of the adaptation produced by bleaching. Our experiments demonstrate that in mammalian rods, as in amphibian rods, steady-state desensitization after bleaching is produced by two components: (1) a reduction in the probability of photon absorption produced by a decrease in rhodopsin concentration; and (2) an equivalent background light whose intensity is proportional to the fraction of bleached pigment, and which adapts the rod like real background light. These two mechanisms together fully account for the ‘log-linear' relationship in mammalian retina between sensitivity and per cent bleach, which can be measured in the steady state following exposure to bright light. Our methods will now make possible an examination of bleaching adaptation and pigment regeneration in mouse animal lines with mutations or other alterations in the proteins of transduction.

摘要

当杆状光感受器中的大量视紫红质暴露于强光下时,杆状细胞会通过一种称为漂白适应的过程脱敏。在两栖动物的分离光感受器实验中已经揭示了漂白适应的许多特征,但到目前为止,在哺乳动物中还无法进行此类实验。我们现在描述了一种从分离的小鼠杆或小鼠视网膜的小块中进行广泛漂白暴露的微分光光度法测量色素浓度和抽吸电极记录电响应的方法。我们表明,如果在牛血清白蛋白 (BSA) 的存在下以低速率使色素漂白,并允许中间光产物衰减,则小鼠杆状细胞会稳定脱敏;随后用外源性 11-顺式视黄醛处理会导致色素再生,并使对暗适应值的敏感性恢复到很大程度。稳定漂白的野生型 (WT) 杆状细胞显示循环电流减小和衰减时间进程加速,就像在稳定背景光下一样;在鸟苷酸环化酶激活蛋白敲除 (GCAPs(-/-)) 杆状细胞中也观察到类似的效应,表明鸟苷酸环化酶的调节对于漂白产生的适应的至少一部分是不必要的。我们的实验表明,在哺乳动物的杆状细胞中,与两栖动物的杆状细胞一样,漂白后的稳态脱敏是由两个组成部分产生的:(1) 由于视紫红质浓度降低而导致的光子吸收概率降低;(2) 一个等效的背景光,其强度与漂白色素的分数成正比,并且像真实的背景光一样适应杆状细胞。这两个机制共同完全解释了在哺乳动物视网膜中灵敏度与漂白百分比之间的“对数线性”关系,这种关系可以在暴露于强光后的稳态下进行测量。我们的方法现在将使在具有转导蛋白突变或其他改变的小鼠动物系中检查漂白适应和色素再生成为可能。

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