杆状双极细胞的进化与杆状视觉。

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Rikard Frederiksen, Yi-Rong Peng, Alapakkam P Sampath, Gordon L Fain
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引用次数: 0

摘要

双极细胞是脊椎动物视网膜中间神经元,将杆状和锥状光感受器的信号传递给无突细胞和神经节细胞。双极细胞存在于所有脊椎动物中,与光感受器具有许多结构和分子亲和力;它们可能在脊椎动物进化的早期与杆状和锥状祖先一起出现。有两种类型的双极细胞,以去极化(ON)或超极化(OFF)响应中央照明。在大多数脊椎动物物种中,视杆信号被传递给专门的视杆双极细胞,这些细胞将来自许多视杆的信号汇总起来,便于在视觉阈值处进行检测。七鳃鳗是在寒武纪晚期从所有其他脊椎动物中分化出来的,它同时具有杆ON和杆OFF双极细胞,但哺乳动物只有杆ON细胞。哺乳动物的杆状细胞信号通过AII(或A2)无突细胞间接传递到输出神经元,这些细胞连接到锥ON和锥OFF双极细胞,然后再连接到神经节细胞。这些发现提出了在视网膜进化过程中rod OFF双极细胞何时丢失的问题。由于对软骨鱼(角鲨)和尾尾动物(蝾螈)的杆状OFF双极细胞进行了生理记录,杆状OFF双极细胞及其回路至少在泥盆纪之前一直保留在脊椎动物祖先中。最近的证据表明,斑马鱼视网膜处理杆状信号的过程与哺乳动物相似,这表明杆状OFF双极细胞至少丢失了两次。单独使用棒ON双极细胞可能提供了一种选择性优势,从增加的信号到噪声辨别接近视觉阈值。杆状细胞和锥状细胞在结构和分子上与双极细胞有许多相似之处,双极细胞是视网膜的中间神经元,将光感受器的信号传递到视网膜输出端。双极细胞可以是ON(中心去极化)或OFF(中心超极化),杆状或锥体占主导地位。七鳃鳗在5亿年前从所有其他脊椎动物中分化出来,具有ON和OFF双极细胞,它们可以是杆状或锥体显性的。我们认为,这种独立的杆/锥双极细胞通路的配置是早期脊椎动物的代表。杆ON和杆OFF双极至少持续到泥盆纪两栖动物的祖先,但哺乳动物和硬骨鱼只有杆ON双极细胞,并通过专门的无突细胞传递杆OFF信号。我们认为,在脊椎动物进化过程中,至少在两个不同的谱系中,杆状OFF双极细胞丢失了,可能是为了增加杆状视觉的信噪比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evolution of rod bipolar cells and rod vision.

Bipolar cells are vertebrate retinal interneurons conveying signals from rod and cone photoreceptors to amacrine and ganglion cells. Bipolar cells are found in all vertebrates and have many structural and molecular affinities with photoreceptors; they probably appeared very early during vertebrate evolution in conjunction with rod and cone progenitors. There are two types of bipolar cells, responding to central illumination with depolarization (ON) or hyperpolarization (OFF). In most vertebrate species, rod signals are conveyed to specialized rod bipolar cells, which sum signals from many rods and facilitate detection at the visual threshold. Lamprey, which diverged from all other vertebrates in the late Cambrian, have both rod ON and rod OFF bipolar cells, but mammals have only rod ON cells. Rod signals in mammals are conveyed to output neurons indirectly via AII (or A2) amacrine cells, which synapse onto cone ON and cone OFF bipolar-cells and then to ganglion cells. These findings raise the question of when during retinal evolution rod OFF bipolar cells were lost. Because physiological recordings have been made from rod OFF bipolar cells in both cartilaginous fishes (dogfish) and urodeles (salamanders), rod OFF bipolar cells and their circuits must have been retained in vertebrate progenitors at least until the Devonian. Recent evidence showing that zebrafish retina processes rod signals similar to those in mammals indicates that rod OFF bipolar cells were lost at least twice. The sole utilization of rod ON bipolar cells may have provided a selective advantage from increased signal-to-noise discrimination near the visual threshold. KEY POINTS: Rods and cones have many structural and molecular similarities to bipolar cells, which are retinal interneurons conveying signals from photoreceptors to the retinal output. Bipolar cells can be either ON (centre depolarizing) or OFF (centre hyperpolarizing) and either rod or cone dominant. Lamprey, which diverged from all other vertebrates 500 million years ago, have both ON and OFF bipolar cells, which can each be either rod or cone dominant. We argue that this configuration of separate rod/cone bipolar-cell pathways is representative of early vertebrates. Rod ON and rod OFF bipolars persisted at least until the progenitors of amphibians in the Devonian, but mammals and teleost fishes have only rod ON bipolar cells and convey rod OFF signals via a specialized amacrine cell. We argue that rod OFF bipolar cells were lost in at least two different lineages during vertebrate evolution, probably to increase the signal-to-noise of rod vision.

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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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