Microcircuit Rules Governing Impact of Single Interneurons on Purkinje Cell Output In Vivo

Summary: The functional impact of single interneurons on neuronal output in vivo and how interneurons are recruited by physiological activity patterns remain poorly understood. In the cerebellar cortex, molecular layer interneurons and their targets, Purkinje cells, receive excitatory inputs from gr...

Full description

Bibliographic Details
Main Authors: Charlotte Arlt, Michael Häusser
Format: Article
Language:English
Published: Elsevier 2020-03-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124720301637
_version_ 1818451049933963264
author Charlotte Arlt
Michael Häusser
author_facet Charlotte Arlt
Michael Häusser
author_sort Charlotte Arlt
collection DOAJ
description Summary: The functional impact of single interneurons on neuronal output in vivo and how interneurons are recruited by physiological activity patterns remain poorly understood. In the cerebellar cortex, molecular layer interneurons and their targets, Purkinje cells, receive excitatory inputs from granule cells and climbing fibers. Using dual patch-clamp recordings from interneurons and Purkinje cells in vivo, we probe the spatiotemporal interactions between these circuit elements. We show that single interneuron spikes can potently inhibit Purkinje cell output, depending on interneuron location. Climbing fiber input activates many interneurons via glutamate spillover but results in inhibition of those interneurons that inhibit the same Purkinje cell receiving the climbing fiber input, forming a disinhibitory motif. These interneuron circuits are engaged during sensory processing, creating diverse pathway-specific response functions. These findings demonstrate how the powerful effect of single interneurons on Purkinje cell output can be sculpted by various interneuron circuit motifs to diversify cerebellar computations. : Using dual two-photon guided patch-clamp recordings from molecular-layer interneurons and Purkinje cells in vivo, Arlt and Häusser show that single-interneuron spikes can potently inhibit Purkinje cell output and uncover the microcircuit logic by which interneurons and their targets are recruited by different excitatory afferents. Keywords: cerebellum, Purkinje cell, interneuron, patch clamp, inhibition, climbing fiber, glutamate spillover, in vivo, two-photon imaging, synaptic integration
first_indexed 2024-12-14T21:01:01Z
format Article
id doaj.art-901e8834b8b54c648ad841946a51921d
institution Directory Open Access Journal
issn 2211-1247
language English
last_indexed 2024-12-14T21:01:01Z
publishDate 2020-03-01
publisher Elsevier
record_format Article
series Cell Reports
spelling doaj.art-901e8834b8b54c648ad841946a51921d2022-12-21T22:47:35ZengElsevierCell Reports2211-12472020-03-0130930203035.e3Microcircuit Rules Governing Impact of Single Interneurons on Purkinje Cell Output In VivoCharlotte Arlt0Michael Häusser1Wolfson Institute for Biomedical Research and Department of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London WC1E 6BT, UKWolfson Institute for Biomedical Research and Department of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London WC1E 6BT, UK; Corresponding authorSummary: The functional impact of single interneurons on neuronal output in vivo and how interneurons are recruited by physiological activity patterns remain poorly understood. In the cerebellar cortex, molecular layer interneurons and their targets, Purkinje cells, receive excitatory inputs from granule cells and climbing fibers. Using dual patch-clamp recordings from interneurons and Purkinje cells in vivo, we probe the spatiotemporal interactions between these circuit elements. We show that single interneuron spikes can potently inhibit Purkinje cell output, depending on interneuron location. Climbing fiber input activates many interneurons via glutamate spillover but results in inhibition of those interneurons that inhibit the same Purkinje cell receiving the climbing fiber input, forming a disinhibitory motif. These interneuron circuits are engaged during sensory processing, creating diverse pathway-specific response functions. These findings demonstrate how the powerful effect of single interneurons on Purkinje cell output can be sculpted by various interneuron circuit motifs to diversify cerebellar computations. : Using dual two-photon guided patch-clamp recordings from molecular-layer interneurons and Purkinje cells in vivo, Arlt and Häusser show that single-interneuron spikes can potently inhibit Purkinje cell output and uncover the microcircuit logic by which interneurons and their targets are recruited by different excitatory afferents. Keywords: cerebellum, Purkinje cell, interneuron, patch clamp, inhibition, climbing fiber, glutamate spillover, in vivo, two-photon imaging, synaptic integrationhttp://www.sciencedirect.com/science/article/pii/S2211124720301637
spellingShingle Charlotte Arlt
Michael Häusser
Microcircuit Rules Governing Impact of Single Interneurons on Purkinje Cell Output In Vivo
Cell Reports
title Microcircuit Rules Governing Impact of Single Interneurons on Purkinje Cell Output In Vivo
title_full Microcircuit Rules Governing Impact of Single Interneurons on Purkinje Cell Output In Vivo
title_fullStr Microcircuit Rules Governing Impact of Single Interneurons on Purkinje Cell Output In Vivo
title_full_unstemmed Microcircuit Rules Governing Impact of Single Interneurons on Purkinje Cell Output In Vivo
title_short Microcircuit Rules Governing Impact of Single Interneurons on Purkinje Cell Output In Vivo
title_sort microcircuit rules governing impact of single interneurons on purkinje cell output in vivo
url http://www.sciencedirect.com/science/article/pii/S2211124720301637
work_keys_str_mv AT charlottearlt microcircuitrulesgoverningimpactofsingleinterneuronsonpurkinjecelloutputinvivo
AT michaelhausser microcircuitrulesgoverningimpactofsingleinterneuronsonpurkinjecelloutputinvivo