Efficiency of Information Transmission by Retinal Ganglion Cells

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Efficiency of Information Transmission by Retinal Ganglion Cells Kristin Koch, Judith McLean, Michael Berry, Peter Sterling, Vijay Balasubramanian, Michael A. Freed  Current Biology  Volume 14, Issue 17, Pages 1523-1530 (September 2004) DOI: 10.1016/j.cub.2004.08.060

Figure 1 Standard Stimuli Drive Brisk and Sluggish Cells at Different Rates Stimulus was either a spatially homogeneous flicker or a flickering checkerboard optimized for the receptive field center. Stimulus sequence was typically repeated 80 times to obtain jitter, peak rates for firing events, and the overall mean rate for the entire recording. OFF brisk-transient cell: Spatially homogeneous stimulus-evoked reproducible firing events with a firing precision (jitter) of 3 ms. Peak rate during an event and average rate for entire response were high (375 and 8.3 spikes s−1). Checkerboard evoked a similar number of events with the same precision (3 ms) and similar peak and average rates (369 and 9 spikes s−1). Local-edge cell: Spatially homogeneous stimulus evoked few events, which were reproducible with a precision of 11 ms. Peak and average rates were low (44 and 0.4 spikes s−1). Checkerboard evoked more firing events with a similar precision (10 ms). Peak and average rates were greater than for the spatially homogeneous stimulus (170 and 3.3 spikes s−1). Current Biology 2004 14, 1523-1530DOI: (10.1016/j.cub.2004.08.060)

Figure 2 Responses of Brisk-Sustained and Directionally Selective Cells to Flicker over the Receptive Field Center Check size was optimized to evoke the highest firing rate from each cell. OFF brisk-sustained cell fired precisely (4 ms) with high peak and average firing rates (241 and 32 spikes s−1). ON-OFF DS cell (dendrites shown separately for off and on strata) responded about as precisely as brisk cell (5 ms) but at lower rates (141 and 2.7 spikes s−1). ON DS cell responded less precisely than brisk cell (12 ms) and at lower rates (77 and 16 spikes s−1). Generally, sluggish cells fired less precisely than brisk cells and at lower rates. Current Biology 2004 14, 1523-1530DOI: (10.1016/j.cub.2004.08.060)

Figure 3 Brisk and Sluggish Cells Transmit Information with Similar Efficiency (A–C) Solid line was calculated from the equation for coding capacity C(R, Δt) versus average firing rate (R) with bin width Δt = 5 ms (see text). Dashed line is a constant percentage of C(R, Δt), adjusted for best fit to information rate, total entropy, or noise entropy. For example, in A, dashed line is 0.33 * C(R, Δt), denoting that information efficiency is 33%. K2 is the coefficient of nondetermination, i.e., the percentage of the total variance comprised by the vertical deviations of data points from the dashed line. (D) Information per spike declines with increasing rate. Dashed line is the equation for information efficiency divided by firing rate, 0.33 C(R, Δt)/R. Current Biology 2004 14, 1523-1530DOI: (10.1016/j.cub.2004.08.060)

Figure 4 Quantifying Spike Train's Temporal Correlations and Noisiness Upper graph: Negative Zentropy was greater for brisk than for sluggish cells. Zentropy for both classes resembled that of their respective rate-modulated Poisson simulation, reflecting similar temporal correlations. Lower graph: Fano factor (a measure of noise) was smaller for real cells than for the Poisson simulation. Current Biology 2004 14, 1523-1530DOI: (10.1016/j.cub.2004.08.060)

Figure 5 Spike Trains and Rate-Modulated Poisson Process Have Similar Information Rates, Total Entropy, and Noise Entropy The information rate, total entropy, and noise entropy of brisk and sluggish cells are graphed against the same measures from the Poisson simulation (symbols same as Figure 3). Linear regression fits are constrained to pass through the origin. Deviation of information rate from a regression fit was only 10% of its total variance (K2 = coefficient of nondetermination). Similarly, total entropy and noise entropy deviated by only 2%. By this standard, the efficiency of information transmission is similar for all cells. Current Biology 2004 14, 1523-1530DOI: (10.1016/j.cub.2004.08.060)