Müller glial cell photosensitivity: A novel function bringing higher complexity to vertebrate retinal physiology

Natalia A. Marchese , Maximiliano N. Ríos , Mario E. Guido
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Abstract

The retina of vertebrates is responsible for detecting and capturing ambient light for image and non-image forming (NIF) functions through diverse projections to the brain which regulate visual processing, pupillary light responses, photic synchronization of circadian rhythms and suppression of pineal melatonin, among others. For this, vertebrates have retained through evolution at least two sets of photoreceptors specialized primarily in such visual and NIF tasks: visual photoreceptors cones and rods responsible for day/night vision, and intrinsically photosensitive retinal ganglion cells (ipRGC) together with horizontal cells in some vertebrates, expressing melanopsin (Opn4). Interestingly, Opn4 as well as encephalopsin (Opn3) and neuropsin (Opn5), responding to blue and UV light, respectively, are expressed in the inner retina and command light detection in the blue range of the visible spectra; they are responsible for a number of NIF functions still lacking characterization. Though most retinal photoreceptors are derived from ciliary or neuronal progenitor cells, in recent years Müller glial cells (MCs), the most abundant retinal glial cell type, have been shown to express different blue opsins (Opn3 and Opn5) and the photoisomerase retinal G protein-coupled receptor (RGR), and to respond directly to light. MCs display different essential functions to maintain the homeostasis and cell survival of the whole retina, contributing to glutamate metabolism and chromophore recycling. The novel photoreceptive capacity of MCs, mainly in the blue region, offers several highly intriguing possibilities that increase the complexity levels for light detection in the retina and its light-activated circuits, calling for further investigation. The goal of the present review is to discuss the state of the art of research on the principal macroglial cells in the retina, focusing mainly on the novel photic responses driven by MCs, the biochemical mechanisms triggered after light stimulation and their putative functions and implications.

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神经胶质细胞光敏性:一种新的功能,给脊椎动物视网膜生理带来更高的复杂性
脊椎动物的视网膜负责检测和捕获环境光,以实现图像和非图像形成(NIF)功能,通过向大脑的各种投影来调节视觉处理、瞳孔光反应、昼夜节律的光同步和松果体褪黑激素的抑制等。为此,脊椎动物在进化过程中保留了至少两套主要用于视觉和NIF任务的光感受器:负责昼夜视觉的视锥细胞和视杆细胞,以及一些脊椎动物的内在光敏视网膜神经节细胞(ipRGC)和水平细胞,表达黑视素(Opn4)。有趣的是,Opn4以及脑视蛋白(Opn3)和神经视蛋白(Opn5)分别在视网膜内部表达,并在可见光谱的蓝色范围内进行光检测;它们负责许多仍缺乏表征的NIF功能。虽然大多数视网膜光感受器来源于睫状体或神经元祖细胞,但近年来研究表明,最丰富的视网膜神经胶质细胞类型神经胶质细胞(MCs)表达不同的蓝色视蛋白(Opn3和Opn5)和光异构酶视网膜G蛋白偶联受体(RGR),并直接对光作出反应。MCs在维持整个视网膜的稳态和细胞存活中发挥着不同的基本功能,参与谷氨酸代谢和发色团循环。主要在蓝色区域的MCs的新光感受能力提供了几个非常有趣的可能性,增加了视网膜及其光激活电路中光探测的复杂性,需要进一步研究。本文就视网膜中主要的大胶质细胞的研究现状作一综述,重点介绍由MCs驱动的新型光反应、光刺激后引发的生化机制及其可能的功能和意义。
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