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Lookup NU author(s): Dr Gerrit Hilgen, Professor Evelyne SernagorORCiD
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Computing the spike-triggered average (STA) is a simple method to estimate linear receptive fields (RFs) in sensory neurons. For random, uncorrelated stimuli, the STA provides an unbiased RF estimate, but in practice, white noise at high resolution is not an optimal stimulus choice as it usually evokes only weak responses. Therefore, for a visual stimulus, images of randomly modulated blocks of pixels are often used. This solution naturally limits the resolution at which an RF can be measured. Here, we present a simple super-resolution technique that can overcome these limitations. We define a novel stimulus type, the shifted white noise (SWN), by introducing random spatial shifts in the usual stimulus to increase the resolution of the measurements. In simulated data, we show that the average error using the SWN was 1.7 times smaller than when using the classical stimulus, with successful mapping of 2.3 times more neurons, covering a broader range of RF sizes. Moreover, successful RF mapping was achieved with brief recordings of light responses, lasting only about 1 min of activity, which is more than 10 times more efficient than the classical white noise stimulus. In recordings from mouse retinal ganglion cells with large scale multielectrode arrays, we successfully mapped 21 times more RFs than when using the traditional white noise stimuli. In summary, randomly shifting the usual white noise stimulus significantly improves RFs estimation, and requires only short recordings.NEW & NOTEWORTHY We present a novel approach to measure receptive fields in large and heterogeneous populations of sensory neurons recorded with large-scale, high-density multielectrode arrays. Our approach leverages super-resolution principles to improve the yield of the spike-triggered average method. By simply designing a new stimulus, we provide experimentalists with a new and fast technique to simultaneously detect more receptive fields at higher resolution in population of hundreds to thousands of neurons.
Author(s): Pamplona D, Hilgen G, Hennig MH, Cessac B, Sernagor E, Kornprobst P
Publication type: Article
Publication status: Published
Journal: Journal of Neurophysiology
Year: 2022
Volume: 127
Issue: 5
Pages: 1334-1347
Print publication date: 01/05/2022
Online publication date: 29/04/2022
Acceptance date: 03/02/2022
ISSN (print): 0022-3077
ISSN (electronic): 1522-1598
Publisher: American Physiological Society
URL: https://doi.org/10.1152/jn.00076.2021
DOI: 10.1152/jn.00076.2021
PubMed id: 35235437
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