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      Rapid neural coding in the mouse retina with the first wave of spikes

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      1 , , 2 , 2 , 3 , 4 , 1
      BMC Neuroscience
      BioMed Central
      The Twenty Third Annual Computational Neuroscience Meeting: CNS*2014
      26-31 July 2014

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          Abstract

          For flashed stimuli presentations, it is known that the latency of the first spike of retinal ganglion cells (RGC) encodes information about the stimulus. This was shown at the level of individual neurons but also at the population level by considering the relative latency between certain pairs of RGC [1]. In this work, we further investigated this population code on mouse retinas using a 60-channel MEA (469 RGC pooled from 5 retinas) in response to gratings of varying phase, spatial frequency. Interestingly, due to the presence of a high spontaneous activity, we did not find any RGC pair showing a clear relation between the relative latencies and stimuli as in [1]. So we extended this analysis to the whole population instead of looking at individual pairs, by considering the relative order of all spike latencies, i.e. the shape of the first wave of spikes (FWS) after stimulus onset. We first showed that the FWS is specific to each stimuli. To do so, we defined a distance between the FWS of a reference grating and the gratings with similar spatial frequency and varying phases. This distance was correlated to the phase difference between gratings. Then, to estimate quantitatively the coding efficiency of the FWS, we performed a discrimination task where the aim was to identify the phase among gratings of identical spatial frequency. We compared the performance (fraction of correct predictions, FCP) of the FWS under classical Bayesian decoders to independent response latency of each recorded RGC. Results showed the FWS decoder which is based on the relative rank of latencies only, was as efficient as the pure latency decoder based on absolute latency values (~73% of FCP for both). Finally, as the spikes from the output of the retina are conveyed and processed by higher neural structure such as the Lateral Geniculate Nucleus (LGN), we investigated the possible effects of an a posteriori processing stage on the neural code. We fed a simulated LGN-like layer [2] with the spikes obtained from our recordings. We then analyzed the output spikes from the simulated LGN using the same discrimination task. As the number of RGC increased, the FWS decoder rapidly outperforms the latency decoder. Considering all RGC, we compared the performance obtained before and after the LGN. Results showed the latency decoder discrimination performance decreased (from 73% to 40% of FCP) although the FWS decoder discrimination performance remained more stable (from 73% to 70% of FCP).

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          Rapid neural coding in the retina with relative spike latencies.

          Natural vision is a highly dynamic process. Frequent body, head, and eye movements constantly bring new images onto the retina for brief periods, challenging our understanding of the neural code for vision. We report that certain retinal ganglion cells encode the spatial structure of a briefly presented image in the relative timing of their first spikes. This code is found to be largely invariant to stimulus contrast and robust to noisy fluctuations in response latencies. Mechanistically, the observed response characteristics result from different kinetics in two retinal pathways ("ON" and "OFF") that converge onto ganglion cells. This mechanism allows the retina to rapidly and reliably transmit new spatial information with the very first spikes emitted by a neural population.
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            Relative spike time coding and STDP-based orientation selectivity in the early visual system in natural continuous and saccadic vision: a computational model.

            We have built a phenomenological spiking model of the cat early visual system comprising the retina, the Lateral Geniculate Nucleus (LGN) and V1's layer 4, and established four main results (1) When exposed to videos that reproduce with high fidelity what a cat experiences under natural conditions, adjacent Retinal Ganglion Cells (RGCs) have spike-time correlations at a short timescale (~30 ms), despite neuronal noise and possible jitter accumulation. (2) In accordance with recent experimental findings, the LGN filters out some noise. It thus increases the spike reliability and temporal precision, the sparsity, and, importantly, further decreases down to ~15 ms adjacent cells' correlation timescale. (3) Downstream simple cells in V1's layer 4, if equipped with Spike Timing-Dependent Plasticity (STDP), may detect these fine-scale cross-correlations, and thus connect principally to ON- and OFF-centre cells with Receptive Fields (RF) aligned in the visual space, and thereby become orientation selective, in accordance with Hubel and Wiesel (Journal of Physiology 160:106-154, 1962) classic model. Up to this point we dealt with continuous vision, and there was no absolute time reference such as a stimulus onset, yet information was encoded and decoded in the relative spike times. (4) We then simulated saccades to a static image and benchmarked relative spike time coding and time-to-first spike coding w.r.t. to saccade landing in the context of orientation representation. In both the retina and the LGN, relative spike times are more precise, less affected by pre-landing history and global contrast than absolute ones, and lead to robust contrast invariant orientation representations in V1.
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              Author and article information

              Contributors
              Conference
              BMC Neurosci
              BMC Neurosci
              BMC Neuroscience
              BioMed Central
              1471-2202
              2014
              21 July 2014
              : 15
              : Suppl 1
              : P120
              Affiliations
              [1 ]Neuromathcomp, INRIA, Sophia Antipolis, 06902, France
              [2 ]Institute of Neuroscience, Medical School, Newcastle University, Newcastle UK
              [3 ]Institut de la Vision, UPMC Université Paris 06, Paris, 75012, France
              [4 ]CNRS, UMR 7210, Paris, 75012, France
              Article
              1471-2202-15-S1-P120
              10.1186/1471-2202-15-S1-P120
              4125003
              bedf4716-7d5b-407d-bbde-3fdb566804b8
              Copyright © 2014 Portelli et al; licensee BioMed Central Ltd.

              This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

              The Twenty Third Annual Computational Neuroscience Meeting: CNS*2014
              Québec City, Canada
              26-31 July 2014
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              Neurosciences
              Neurosciences

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