Dendritic axon origin enables information gating by perisomatic inhibition in pyramidal neurons.


Journal

Science (New York, N.Y.)
ISSN: 1095-9203
Titre abrégé: Science
Pays: United States
ID NLM: 0404511

Informations de publication

Date de publication:
23 09 2022
Historique:
entrez: 22 9 2022
pubmed: 23 9 2022
medline: 28 9 2022
Statut: ppublish

Résumé

Information processing in neuronal networks involves the recruitment of selected neurons into coordinated spatiotemporal activity patterns. This sparse activation results from widespread synaptic inhibition in conjunction with neuron-specific synaptic excitation. We report the selective recruitment of hippocampal pyramidal cells into patterned network activity. During ripple oscillations in awake mice, spiking is much more likely in cells in which the axon originates from a basal dendrite rather than from the soma. High-resolution recordings in vitro and computer modeling indicate that these spikes are elicited by synaptic input to the axon-carrying dendrite and thus escape perisomatic inhibition. Pyramidal cells with somatic axon origin can be activated during ripple oscillations by blocking their somatic inhibition. The recruitment of neurons into active ensembles is thus determined by axonal morphological features.

Identifiants

pubmed: 36137045
doi: 10.1126/science.abj1861
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1448-1452

Auteurs

Alexander Hodapp (A)

Institute of Physiology and Pathophysiology, Medical Faculty, Heidelberg University, Heidelberg, Germany.

Martin E Kaiser (ME)

Institute of Physiology and Pathophysiology, Medical Faculty, Heidelberg University, Heidelberg, Germany.

Christian Thome (C)

Institute of Physiology and Pathophysiology, Medical Faculty, Heidelberg University, Heidelberg, Germany.
Institute of Anatomy and Cell Biology, Medical Faculty, Johannes Kepler University, Linz, Austria.
Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, CA, USA.

Lingjun Ding (L)

Institute of Neurobiology, University of Tübingen, Tübingen, Germany.
Werner-Reichardt Centre for Integrative Neuroscience, Tübingen, Germany.
Graduate Training Centre of Neuroscience, IMPRS, Tübingen, Germany.

Andrei Rozov (A)

Institute of Physiology and Pathophysiology, Medical Faculty, Heidelberg University, Heidelberg, Germany.
Federal Center of Brain Research and Neurotechnologies, Moscow, Russian Federation.
OpenLab of Neurobiology, Kazan Federal University, Kazan, Russian Federation.

Matthias Klumpp (M)

Institute of Physiology and Pathophysiology, Medical Faculty, Heidelberg University, Heidelberg, Germany.

Nikolas Stevens (N)

Institute of Physiology and Pathophysiology, Medical Faculty, Heidelberg University, Heidelberg, Germany.

Moritz Stingl (M)

Institute of Physiology and Pathophysiology, Medical Faculty, Heidelberg University, Heidelberg, Germany.

Tina Sackmann (T)

Institute of Physiology and Pathophysiology, Medical Faculty, Heidelberg University, Heidelberg, Germany.

Nadja Lehmann (N)

Institute of Neuroanatomy, Mannheim Center for Translational Neuroscience (MCTN), Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.

Andreas Draguhn (A)

Institute of Physiology and Pathophysiology, Medical Faculty, Heidelberg University, Heidelberg, Germany.

Andrea Burgalossi (A)

Institute of Neurobiology, University of Tübingen, Tübingen, Germany.
Werner-Reichardt Centre for Integrative Neuroscience, Tübingen, Germany.

Maren Engelhardt (M)

Institute of Anatomy and Cell Biology, Medical Faculty, Johannes Kepler University, Linz, Austria.
Institute of Neuroanatomy, Mannheim Center for Translational Neuroscience (MCTN), Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.

Martin Both (M)

Institute of Physiology and Pathophysiology, Medical Faculty, Heidelberg University, Heidelberg, Germany.

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