| Literature DB >> 27275008 |
Geoffrey Portelli1, John M Barrett2, Gerrit Hilgen2, Timothée Masquelier3, Alessandro Maccione4, Stefano Di Marco4, Luca Berdondini4, Pierre Kornprobst1, Evelyne Sernagor2.
Abstract
How a population of retinal ganglion cells (RGCs) encodes the visual scene remains an open question. Going beyond individual RGC coding strategies, results in salamander suggest that the relative latencies of a RGC pair encode spatial information. Thus, a population code based on this concerted spiking could be a powerful mechanism to transmit visual information rapidly and efficiently. Here, we tested this hypothesis in mouse by recording simultaneous light-evoked responses from hundreds of RGCs, at pan-retinal level, using a new generation of large-scale, high-density multielectrode array consisting of 4096 electrodes. Interestingly, we did not find any RGCs exhibiting a clear latency tuning to the stimuli, suggesting that in mouse, individual RGC pairs may not provide sufficient information. We show that a significant amount of information is encoded synergistically in the concerted spiking of large RGC populations. Thus, the RGC population response described with relative activities, or ranks, provides more relevant information than classical independent spike count- or latency- based codes. In particular, we report for the first time that when considering the relative activities across the whole population, the wave of first stimulus-evoked spikes is an accurate indicator of stimulus content. We show that this coding strategy coexists with classical neural codes, and that it is more efficient and faster. Overall, these novel observations suggest that already at the level of the retina, concerted spiking provides a reliable and fast strategy to rapidly transmit new visual scenes.Entities:
Keywords: ganglion cells; multielectrode array; population coding; rank order coding; retina
Mesh:
Year: 2016 PMID: 27275008 PMCID: PMC4891767 DOI: 10.1523/ENEURO.0134-15.2016
Source DB: PubMed Journal: eNeuro ISSN: 2373-2822