From serial to parallel: predicting synchronous firing of large neural populations from sequential recordings

Author:

Sorochynskyi Oleksandr,Deny Stéphane,Marre Olivier,Ferrari Ulisse

Abstract

A major goal in neuroscience is to understand how populations of neurons code for stimuli or actions. While the number of neurons that can be recorded simultaneously is increasing at a fast pace, in most cases these recordings cannot access a complete population: some neurons that carry relevant information remain unrecorded. In particular, it is hard to simultaneously record all the neurons of the same type in a given area. Recent progress has made possible to determine the type of each recorded neuron in a given area thanks to genetic and physiological tools. However, it is unclear how to infer the activity of a full population of neurons of the same type from sequential recordings across different experiments. Neural networks exhibit collective behaviour, e.g. noise correlations and synchronous activity, that are not directly captured by a conditionally-independent model that would just pool together the spike trains from sequential recordings. Here we present a method to build population activity from single cell responses taken from sequential recordings, which only requires pairwise recordings to train the model. Our method combines copula distributions and maximum entropy modeling. After training, the model allows us to predict the activity of large populations using only sequential recordings of single cells. We applied this method to a population of ganglion cells, the retinal output, all belonging to the same type. From just the spiking response of each cell to a repeated stimulus, we could predict the full activity of the population. We could then generalize to predict the population responses to different stimuli and even to different experiments. As a result, we were able to use our approach to construct a synthetic model of a very large neuronal population, which uses data combined from multiple experiments. We then predicted the extent of synchronous activity and showed it grew with the number of neurons. This approach is a promising way to infer population activity from sequential recordings in sensory areas.

Publisher

Cold Spring Harbor Laboratory

Reference43 articles.

1. Large-scale recording of neuronal ensembles

2. Simultaneous all-optical manipulation and recording of neural circuit activity with cellular resolution in vivo;Nature methods,2014

3. Recording of a large and complete population in the retina;Journal of Neuroscience,2012

4. Organization of Vomeronasal Sensory Coding Revealed by Fast Volumetric Calcium Imaging

5. Function first: classifying cell types and circuits of the retina;Current opinion in neurobiology,2019

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