Volume 83, Issue 1, Pages (July 2014)

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Volume 83, Issue 1, Pages 87-92 (July 2014) High-Fidelity Reproduction of Spatiotemporal Visual Signals for Retinal Prosthesis  Lauren H. Jepson, Pawel Hottowy, Geoffrey A. Weiner, Władysław Dabrowski, Alan M. Litke, E.J. Chichilnisky  Neuron  Volume 83, Issue 1, Pages 87-92 (July 2014) DOI: 10.1016/j.neuron.2014.04.044 Copyright © 2014 Elsevier Inc. Terms and Conditions

Figure 1 Spatiotemporal Visual and Electrical Activation of a Complete Local Population of Retinal Ganglion Cells (A) Receptive fields of six ON parasol cells measured in a single recording are shown with ellipses representing the 1 SD contour of a Gaussian fit to the spatial sensitivity profile (see Experimental Procedures). Cell numbers relate to (B). Schematic of moving bar stimulus is shown at left. (B) For each cell, spikes recorded during a single trial of moving bar visual stimulation that was selected for subsequent replication are shown as black dots in the top traces. Times of applied current pulses, derived from the spikes recorded in response to visual stimulation, are shown as arrowheads in the middle traces. Times of spikes recorded during a single electrical stimulation trial are shown as gray dots in the bottom traces. Neuron 2014 83, 87-92DOI: (10.1016/j.neuron.2014.04.044) Copyright © 2014 Elsevier Inc. Terms and Conditions

Figure 2 Responses to Repeated Presentations of Visual and Electrical Stimuli (A) Spike trains elicited by a moving bar visual stimulus are shown for the same cells as in Figure 1, in raster format, with each tick representing the time of a spike, and each row representing a single trial. Coarse vertical band structure for each cell reveals reproducibility of visual responses across trials. (B) Spike trains obtained during electrical stimulation trials with no visual stimulus are shown in the same format as (A). Electrical stimuli (arrowheads above rasters) were delivered at the times of spikes recorded in a single visual stimulation trial (see Figure 1). Precise vertical band structure reflects electrically elicited spikes occurring at a reproducible time in many or all trials. Neuron 2014 83, 87-92DOI: (10.1016/j.neuron.2014.04.044) Copyright © 2014 Elsevier Inc. Terms and Conditions

Figure 3 Inferring Stimulus Speed from Recorded Spike Trains A motion-decoding algorithm (Frechette et al., 2005) based on known features of motion sensing in the primate visual system was used to infer the speed of the moving stimulus from recorded spike trains. This decoding was performed by computing the strength of a motion signal as a function of putative stimulus speed and then identifying the speed that yielded the strongest motion signal. (A) For each recorded trial of visual and electrical stimulation (100 or 50 trials, respectively), the strength of the motion signal extracted from retinal spike trains is shown as a function of putative speed. Vertical line indicates true speed of the visual stimulus. Each black curve was obtained from a single trial of visual stimulation, each gray curve from a single trial of electrical stimulation, from the same six cells as Figures 1 and 2. The white curve represents data from the visual stimulus trial selected for reproduction with electrical stimulation. (B) Variability of speed estimates for visual and electrical stimulation. Histograms in the left panel indicate the speed estimates obtained by identifying the peaks of the curves shown in (A). Top (black) histogram indicates estimates from visual stimulation, bottom (gray) from electrical stimulation. White arrowheads indicate speed estimates of visual stimulus trials chosen for reproduction. Speed estimates were near the true stimulus speed for both kinds of stimulation. Two additional data sets are shown, in the middle (eight cells) and right (six cells) histograms, each with 100 trials of visual and electrical stimulation. In each case, the SDs of speed estimates obtained from visual stimulation (0.058, 0.063, and 0.044 mm/s across preparations) and electrical stimulation (0.050, 0.049, and 0.079 mm/s) were similar. Neuron 2014 83, 87-92DOI: (10.1016/j.neuron.2014.04.044) Copyright © 2014 Elsevier Inc. Terms and Conditions