Abstract

In vivo electrophysiology is the gold standard technique used to investigate sub-second neural dynamics in freely behaving animals. However, monitoring cell-type-specific population activity is not a trivial task. Over the last decade, fiber photometry based on genetically encoded calcium indicators (GECIs) has been widely adopted as a versatile tool to monitor cell-type-specific population activity in vivo. However, this approach suffers from low temporal resolution. Here, we combine these two approaches to monitor both sub-second field potentials and cell-type-specific population activity in freely behaving mice. By developing an economical custom-made system and constructing a hybrid implant of an electrode and a fiber optic cannula, we simultaneously monitor artifact-free mesopontine field potentials and calcium transients in cholinergic neurons across the sleep-wake cycle. We find that mesopontine cholinergic activity co-occurs with sub-second pontine waves, called P-waves, during rapid eye movement sleep. Given the simplicity of our approach, simultaneous electrophysiological recording and cell-type-specific imaging provides a novel and valuable tool for interrogating state-dependent neural circuit dynamics in vivo.

Highlights

  • Intracranial electrophysiological recordings monitor neuronal activity at various spatial scales, from single cells to populations across brain regions, with high temporal resolution (Buzsaki, 2004; Buzsaki et al, 2012; Jun et al, 2017)

  • We focus on pontine waves (P-waves), which were reported in mice recently (Tsunematsu et al, 2020)

  • We show that P-waves during REM sleep co-occurs with calcium transients in mesopontine cholinergic neurons

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Summary

Introduction

Intracranial electrophysiological recordings monitor neuronal activity at various spatial scales, from single cells to populations across brain regions, with high temporal resolution (Buzsaki, 2004; Buzsaki et al, 2012; Jun et al, 2017). Over the last two decades, genetically encoded calcium indicators (GECIs) have been widely used to interrogate neuronal ensemble dynamics, and activity of non-neuronal cells, such as astrocytes in vivo (Nakai et al, 2001; Chen et al, 2013; Stobart et al, 2018; Dana et al, 2019; Inoue et al, 2019; Stringer et al, 2019). Because of the intrinsic nature of calcium signals, the low temporal resolution of GECIs are not ideal for monitoring sub-second

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