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
Summary
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
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.