突触抑制调节视网膜的对比度计算

IF 1.1 4区 医学 Q4 NEUROSCIENCES Visual Neuroscience Pub Date : 2019-01-01 DOI:10.1017/S095252381900004X
Nicholas W Oesch, Jeffrey S Diamond
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引用次数: 0

摘要

抑制通过许多不同类型的细胞介导的多种机制影响神经网络的活动和信号处理。在这里,我们研究了视网膜中的一种 GABA 能中间神经元--A17 氨基细胞--是如何影响视觉信息处理的。我们的研究结果表明,A17会对杆状双极细胞(RBC)突触末端产生相互反馈的抑制性突触,从而扩大RBC突触计算时间对比度的亮度范围,并增强对比度信号在此范围内的可靠性。来自其他羊膜细胞的抑制不会影响这些计算特征。虽然 A17 介导的反馈由 GABAA 和 GABAC 受体共同介导,但后者在扩大对比度计算范围方面起着主要作用。这些结果确定了抑制性中间神经元亚型以及特定突触受体在行为相关神经计算中的特定功能。
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Synaptic inhibition tunes contrast computation in the retina.

Inhibition shapes activity and signal processing in neural networks through numerous mechanisms mediated by many different cell types. Here, we examined how one type of GABAergic interneuron in the retina, the A17 amacrine cell, influences visual information processing. Our results suggest that A17s, which make reciprocal feedback inhibitory synapses onto rod bipolar cell (RBC) synaptic terminals, extend the luminance range over which RBC synapses compute temporal contrast and enhance the reliability of contrast signals over this range. Inhibition from other amacrine cells does not influence these computational features. Although A17-mediated feedback is mediated by both GABAA and GABAC receptors, the latter plays the primary role in extending the range of contrast computation. These results identify specific functions for an inhibitory interneuron subtype, as well as specific synaptic receptors, in a behaviorally relevant neural computation.

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来源期刊
Visual Neuroscience
Visual Neuroscience 医学-神经科学
CiteScore
2.20
自引率
5.30%
发文量
8
审稿时长
>12 weeks
期刊介绍: Visual Neuroscience is an international journal devoted to the publication of experimental and theoretical research on biological mechanisms of vision. A major goal of publication is to bring together in one journal a broad range of studies that reflect the diversity and originality of all aspects of neuroscience research relating to the visual system. Contributions may address molecular, cellular or systems-level processes in either vertebrate or invertebrate species. The journal publishes work based on a wide range of technical approaches, including molecular genetics, anatomy, physiology, psychophysics and imaging, and utilizing comparative, developmental, theoretical or computational approaches to understand the biology of vision and visuo-motor control. The journal also publishes research seeking to understand disorders of the visual system and strategies for restoring vision. Studies based exclusively on clinical, psychophysiological or behavioral data are welcomed, provided that they address questions concerning neural mechanisms of vision or provide insight into visual dysfunction.
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