Department of Ophthalmology & Visual Science, Yale University, New Haven, United States.
Department of Biology, University of Maryland, College Park, United States.
Elife. 2020 May 15;9:e56077. doi: 10.7554/eLife.56077.
Night vision in mammals depends fundamentally on rod photoreceptors and the well-studied rod bipolar (RB) cell pathway. The central neuron in this pathway, the AII amacrine cell (AC), exhibits a spatially tuned receptive field, composed of an excitatory center and an inhibitory surround, that propagates to ganglion cells, the retina's projection neurons. The circuitry underlying the surround of the AII, however, remains unresolved. Here, we combined structural, functional and optogenetic analyses of the mouse retina to discover that surround inhibition of the AII depends primarily on a single interneuron type, the NOS-1 AC: a multistratified, axon-bearing GABAergic cell, with dendrites in both ON and OFF synaptic layers, but with a pure ON (depolarizing) response to light. Our study demonstrates generally that novel neural circuits can be identified from targeted connectomic analyses and specifically that the NOS-1 AC mediates long-range inhibition during night vision and is a major element of the RB pathway.
哺乳动物的夜视功能主要依赖于视杆细胞和研究充分的视杆双极(RB)细胞通路。该通路中的中枢神经元,即 AII 无长突细胞(AC),具有空间调谐的感受野,由一个兴奋中心和一个抑制环绕组成,其信号传递到视网膜的投射神经元——神经节细胞。然而,AII 环绕的神经环路仍未得到解决。在这里,我们结合小鼠视网膜的结构、功能和光遗传学分析,发现 AII 的环绕抑制主要依赖于一种单一的中间神经元类型,即一氧化氮合酶-1 AC:一种多层次、有轴突的 GABA 能细胞,其树突位于 ON 和 OFF 突触层中,但对光表现出纯 ON(去极化)反应。我们的研究表明,通常可以从靶向连接组学分析中识别新的神经回路,并且具体来说,NOS-1 AC 在夜间视觉中介导长程抑制,是 RB 通路的主要组成部分。