Dendrite-Specific Amplification of Weak Synaptic Input during Network Activity In Vivo

Summary: Excitatory synaptic input reaches the soma of a cortical excitatory pyramidal neuron via anatomically segregated apical and basal dendrites. In vivo, dendritic inputs are integrated during depolarized network activity, but how network activity affects apical and basal inputs is not understo...

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Main Authors: Leiron Ferrarese, Jean-Sébastien Jouhanneau, Michiel W.H. Remme, Jens Kremkow, Gergely Katona, Balázs Rózsa, Susanne Schreiber, James F.A. Poulet
Format: Article
Language:English
Published: Elsevier 2018-09-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124718314074
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author Leiron Ferrarese
Jean-Sébastien Jouhanneau
Michiel W.H. Remme
Jens Kremkow
Gergely Katona
Balázs Rózsa
Susanne Schreiber
James F.A. Poulet
author_facet Leiron Ferrarese
Jean-Sébastien Jouhanneau
Michiel W.H. Remme
Jens Kremkow
Gergely Katona
Balázs Rózsa
Susanne Schreiber
James F.A. Poulet
author_sort Leiron Ferrarese
collection DOAJ
description Summary: Excitatory synaptic input reaches the soma of a cortical excitatory pyramidal neuron via anatomically segregated apical and basal dendrites. In vivo, dendritic inputs are integrated during depolarized network activity, but how network activity affects apical and basal inputs is not understood. Using subcellular two-photon stimulation of Channelrhodopsin2-expressing layer 2/3 pyramidal neurons in somatosensory cortex, nucleus-specific thalamic optogenetic stimulation, and paired recordings, we show that slow, depolarized network activity amplifies small-amplitude synaptic inputs targeted to basal dendrites but reduces the amplitude of all inputs from apical dendrites and the cell soma. Intracellular pharmacology and mathematical modeling suggests that the amplification of weak basal inputs is mediated by postsynaptic voltage-gated channels. Thus, network activity dynamically reconfigures the relative somatic contribution of apical and basal inputs and could act to enhance the detectability of weak synaptic inputs. : Ferrarese et al. investigate the impact of network activity on synaptic integration in cortical L2/3 pyramidal neurons in vivo. They report a reduction of apical dendritic inputs but an amplification of small-amplitude basal inputs during depolarized phases of slow network activity. The amplification is dependent on postsynaptic voltage-gated channels.
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spelling doaj.art-387ee88a17d449248fd19612e918f7a92022-12-21T19:18:26ZengElsevierCell Reports2211-12472018-09-01241334553465.e5Dendrite-Specific Amplification of Weak Synaptic Input during Network Activity In VivoLeiron Ferrarese0Jean-Sébastien Jouhanneau1Michiel W.H. Remme2Jens Kremkow3Gergely Katona4Balázs Rózsa5Susanne Schreiber6James F.A. Poulet7Department of Neuroscience, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin-Buch, Robert-Rössle-Str. 10, 13092 Berlin, Germany; Neuroscience Research Center and Cluster of Excellence NeuroCure, Charité-Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, GermanyDepartment of Neuroscience, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin-Buch, Robert-Rössle-Str. 10, 13092 Berlin, Germany; Neuroscience Research Center and Cluster of Excellence NeuroCure, Charité-Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, GermanyDepartment of Biology, Institute for Theoretical Biology, Humboldt-Universität zu Berlin and Bernstein Center for Computational Neuroscience Berlin, Philippstrasse 13, 10115 Berlin, GermanyDepartment of Neuroscience, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin-Buch, Robert-Rössle-Str. 10, 13092 Berlin, Germany; Neuroscience Research Center and Cluster of Excellence NeuroCure, Charité-Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany; Department of Biology, Institute for Theoretical Biology, Humboldt-Universität zu Berlin and Bernstein Center for Computational Neuroscience Berlin, Philippstrasse 13, 10115 Berlin, GermanyLaboratory of 3D Functional Network and Dendritic Imaging, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest 1083, Hungary; MTA-PPKE ITK-NAP B – 2p Measurement Technology Group, The Faculty of Information Technology, Pázmány Péter Catholic University, Budapest 1083, HungaryLaboratory of 3D Functional Network and Dendritic Imaging, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest 1083, Hungary; The Faculty of Information Technology, Pázmány Péter Catholic University, Budapest 1083, HungaryDepartment of Biology, Institute for Theoretical Biology, Humboldt-Universität zu Berlin and Bernstein Center for Computational Neuroscience Berlin, Philippstrasse 13, 10115 Berlin, GermanyDepartment of Neuroscience, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin-Buch, Robert-Rössle-Str. 10, 13092 Berlin, Germany; Neuroscience Research Center and Cluster of Excellence NeuroCure, Charité-Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany; Corresponding authorSummary: Excitatory synaptic input reaches the soma of a cortical excitatory pyramidal neuron via anatomically segregated apical and basal dendrites. In vivo, dendritic inputs are integrated during depolarized network activity, but how network activity affects apical and basal inputs is not understood. Using subcellular two-photon stimulation of Channelrhodopsin2-expressing layer 2/3 pyramidal neurons in somatosensory cortex, nucleus-specific thalamic optogenetic stimulation, and paired recordings, we show that slow, depolarized network activity amplifies small-amplitude synaptic inputs targeted to basal dendrites but reduces the amplitude of all inputs from apical dendrites and the cell soma. Intracellular pharmacology and mathematical modeling suggests that the amplification of weak basal inputs is mediated by postsynaptic voltage-gated channels. Thus, network activity dynamically reconfigures the relative somatic contribution of apical and basal inputs and could act to enhance the detectability of weak synaptic inputs. : Ferrarese et al. investigate the impact of network activity on synaptic integration in cortical L2/3 pyramidal neurons in vivo. They report a reduction of apical dendritic inputs but an amplification of small-amplitude basal inputs during depolarized phases of slow network activity. The amplification is dependent on postsynaptic voltage-gated channels.http://www.sciencedirect.com/science/article/pii/S2211124718314074
spellingShingle Leiron Ferrarese
Jean-Sébastien Jouhanneau
Michiel W.H. Remme
Jens Kremkow
Gergely Katona
Balázs Rózsa
Susanne Schreiber
James F.A. Poulet
Dendrite-Specific Amplification of Weak Synaptic Input during Network Activity In Vivo
Cell Reports
title Dendrite-Specific Amplification of Weak Synaptic Input during Network Activity In Vivo
title_full Dendrite-Specific Amplification of Weak Synaptic Input during Network Activity In Vivo
title_fullStr Dendrite-Specific Amplification of Weak Synaptic Input during Network Activity In Vivo
title_full_unstemmed Dendrite-Specific Amplification of Weak Synaptic Input during Network Activity In Vivo
title_short Dendrite-Specific Amplification of Weak Synaptic Input during Network Activity In Vivo
title_sort dendrite specific amplification of weak synaptic input during network activity in vivo
url http://www.sciencedirect.com/science/article/pii/S2211124718314074
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AT jenskremkow dendritespecificamplificationofweaksynapticinputduringnetworkactivityinvivo
AT gergelykatona dendritespecificamplificationofweaksynapticinputduringnetworkactivityinvivo
AT balazsrozsa dendritespecificamplificationofweaksynapticinputduringnetworkactivityinvivo
AT susanneschreiber dendritespecificamplificationofweaksynapticinputduringnetworkactivityinvivo
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