Abstract

Understanding how neural networks generate activity patterns and communicate with each other requires monitoring the electrical activity from many neurons simultaneously. Perfectly suited tools for addressing this challenge are genetically encoded voltage indicators (GEVIs) because they can be targeted to specific cell types and optically report the electrical activity of individual, or populations of neurons. However, analyzing and interpreting the data from voltage imaging experiments is challenging because high recording speeds and properties of current GEVIs yield only low signal-to-noise ratios, making it necessary to apply specific analytical tools. Here, we present NOSA (Neuro-Optical Signal Analysis), a novel open source software designed for analyzing voltage imaging data and identifying temporal interactions between electrical activity patterns of different origin. In this work, we explain the challenges that arise during voltage imaging experiments and provide hands-on analytical solutions. We demonstrate how NOSA’s baseline fitting, filtering algorithms and movement correction can compensate for shifts in baseline fluorescence and extract electrical patterns from low signal-to-noise recordings. NOSA allows to efficiently identify oscillatory frequencies in electrical patterns, quantify neuronal response parameters and moreover provides an option for analyzing simultaneously recorded optical and electrical data derived from patch-clamp or other electrode-based recordings. To identify temporal relations between electrical activity patterns we implemented different options to perform cross correlation analysis, demonstrating their utility during voltage imaging in Drosophila and mice. All features combined, NOSA will facilitate the first steps into using GEVIs and help to realize their full potential for revealing cell-type specific connectivity and functional interactions.

Highlights

  • One goal of The American BRAIN initiative was to develop methods to comprehend complex activity patterns in specific brain networks and even in whole brains (Alivisatos et al, 2012)

  • Because most Genetically encoded voltage indicators (GEVIs) exhibit decreases in their fluorescence in response to depolarization, NOSA provides the option to invert the relative changes in fluorescence (Figure 1B)

  • While there is sophisticated software for processing imaging recordings (Romano et al, 2017; Giovannucci et al, 2019), NOSA is an entirely open access stand-alone software that requires no installation and comes with an intuitive user-interface that allows to precisely control and comprehend each analytical step. In this manuscript we demonstrate the challenges of performing optical electrophysiology and provide hands-on solutions to extract and analyze electrical patterns from recordings with low signal-tonoise ratio (SNR)

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Summary

INTRODUCTION

One goal of The American BRAIN initiative was to develop methods to comprehend complex activity patterns in specific brain networks and even in whole brains (Alivisatos et al, 2012). GEVIs are being continually improved (Lin and Schnitzer, 2016; Storace et al, 2016), high recording speeds, low signal-to-noise ratios (SNR) and GEVI-specific kinetics bring about unique challenges with respect to data analysis (Yang and St-Pierre, 2016; Kulkarni and Miller, 2017) and require the development of adequate processing software. NOSA includes features for spike- and burst detection, movement artifact compensation, and the ability to analyze simultaneously performed optical and electrical recordings. With these analytical tools, intuitive design, and convenient graphical interface, NOSA should greatly facilitate the first steps into using GEVIs, enabling laboratories around the world to perform and analyze multicellular voltage imaging recordings

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