Dendritic excitations govern back-propagation via a spike-rate accelerometer

Dendrites on neurons support electrical excitations, but the computational significance of these events is not well understood. We developed molecular, optical, and computational tools for all-optical electrophysiology in dendrites. We mapped sub-millisecond voltage dynamics throughout the dendritic trees of CA1 pyramidal neurons under diverse optogenetic and synaptic stimulus patterns, in acute brain slices. Our data show history-dependent spike back-propagation in distal dendrites, driven by locally generated Na<sup>+</sup> spikes (dSpikes). Dendritic depolarization created a transient window for dSpike propagation, opened by A-type K<sub>V</sub> channel inactivation, and closed by slow Na<sub>V</sub> inactivation. Collisions of dSpikes with synaptic inputs triggered calcium channel and N-methyl-D-aspartate receptor (NMDAR)-dependent dendritic plateau potentials and accompanying complex spikes at the soma. This hierarchical ion channel network acts as a spike-rate accelerometer, providing an intuitive picture connecting dendritic biophysics to associative plasticity rules.

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Publication Details

Journal
Nature Communications
Published
2025-02-04
DOI
https://doi.org/10.1038/s41467-025-55819-9
Citations
20
Primary Topic
Photoreceptor and optogenetics research
Type
article
Field-Weighted Citation Impact
18.18

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article

Dendritic excitations govern back-propagation via a spike-rate accelerometer

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20 citations
Nature Communications
Photoreceptor and optogenetics research
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article

Dendritic excitations govern back-propagation via a spike-rate accelerometer

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article en
20 citations

Abstract

Dendrites on neurons support electrical excitations, but the computational significance of these events is not well understood. We developed molecular, optical, and computational tools for all-optical electrophysiology in dendrites. We mapped sub-millisecond voltage dynamics throughout the dendritic trees of CA1 pyramidal neurons under diverse optogenetic and synaptic stimulus patterns, in acute brain slices. Our data show history-dependent spike back-propagation in distal dendrites, driven by locally generated Na<sup>+</sup> spikes (dSpikes). Dendritic depolarization created a transient window for dSpike propagation, opened by A-type K<sub>V</sub> channel inactivation, and closed by slow Na<sub>V</sub> inactivation. Collisions of dSpikes with synaptic inputs triggered calcium channel and N-methyl-D-aspartate receptor (NMDAR)-dependent dendritic plateau potentials and accompanying complex spikes at the soma. This hierarchical ion channel network acts as a spike-rate accelerometer, providing an intuitive picture connecting dendritic biophysics to associative plasticity rules.

Nature CommunicationsVol. 16(1)
Howard Hughes Medical Institute (US), Harvard University (US), Daegu Gyeongbuk Institute of Science and Technology (KR), Janelia Research Campus (US), Harvard University Press (US), Columbia University (US)
National Institutes of Health
Climate action
Openalex Percentile: Top 0%
Photoreceptor and optogenetics research
18.18
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