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

Author:

Hodapp Alexander1ORCID,Kaiser Martin E.1,Thome Christian123ORCID,Ding Lingjun456ORCID,Rozov Andrei178ORCID,Klumpp Matthias1ORCID,Stevens Nikolas1ORCID,Stingl Moritz1,Sackmann Tina1,Lehmann Nadja9ORCID,Draguhn Andreas1ORCID,Burgalossi Andrea45,Engelhardt Maren29ORCID,Both Martin1ORCID

Affiliation:

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

2. Institute of Anatomy and Cell Biology, Medical Faculty, Johannes Kepler University, Linz, Austria.

3. Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, CA, USA.

4. Institute of Neurobiology, University of Tübingen, Tübingen, Germany.

5. Werner-Reichardt Centre for Integrative Neuroscience, Tübingen, Germany.

6. Graduate Training Centre of Neuroscience, IMPRS, Tübingen, Germany.

7. Federal Center of Brain Research and Neurotechnologies, Moscow, Russian Federation.

8. OpenLab of Neurobiology, Kazan Federal University, Kazan, Russian Federation.

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

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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