Cited by 598Neuroscience and Neuropharmacology ResearchIon channel regulation and functionNeural dynamics and brain function

Propagation of action potentials in dendrites depends on dendritic morphology

Vetter, Philipp, Roth, Arnd, Häusser, Michael·2001·Journal of Neurophysiology

Abstract

Action potential propagation links information processing in different regions of the dendritic tree. To examine the contribution of dendritic morphology to the efficacy of propagation, simulations were performed in detailed reconstructions of eight different neuronal types. With identical complements of voltage-gated channels, different dendritic morphologies exhibit distinct patterns of propagation. Remarkably, the range of backpropagation efficacies observed experimentally can be reproduced by the variations in dendritic morphology alone. Dendritic geometry also determines the extent to which modulation of channel densities can affect propagation. Thus in Purkinje cells and dopamine neurons, backpropagation is relatively insensitive to changes in channel densities, whereas in pyramidal cells, backpropagation can be modulated over a wide range. We also demonstrate that forward propagation of dendritically initiated action potentials is influenced by morphology in a similar manner. We show that these functional consequences of the differences in dendritic geometries can be explained quantitatively using simple anatomical measures of dendritic branching patterns, which are captured in a reduced model of dendritic geometry. These findings indicate that differences in dendritic geometry act in concert with differences in voltage-gated channel density and kinetics to generate the diversity in dendritic action potential propagation observed between neurons. They also suggest that changes in dendritic geometry during development and plasticity will critically affect propagation. By determining the spatial pattern of action potential signaling, dendritic morphology thus helps to define the size and interdependence of functional compartments in the neuron.

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Crossref · 10.1152/jn.2001.85.2.926

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Authors
Vetter, P., Roth, A., & Häusser, M.
Affiliations
  • University College London (GB)
  • Max Planck Institute for Medical Research (DE)
  • Max Planck Society (DE)
Venue
Journal of Neurophysiology
Published
2001-02-01
Volume
85
Issue
2
Pages
926-937
ISSN
  • 0022-3077 (ISSN-L)
  • 1522-1598
OpenAlex
W2099676980
Cited by
598
References
1
Citations by year
2026: 10 · 2025: 17 · 2024: 23 · 2023: 16 · 2022: 22 · 2021: 26 · 2020: 21 · 2019: 20 · 2018: 16 · 2017: 26 · 2016: 17 · 2015: 35 · 2014: 28 · 2013: 24 · 2012: 26
FWCI
10.01
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Neurophysiology (publishedVersion)
  • PubMed (publishedVersion)
  • Max Planck Institute for Plasma Physics (submittedVersion)
  • UCL Discovery (University College London) (submittedVersion)
  • The HKU Scholars Hub (University of Hong Kong) (submittedVersion)
  • MPG.PuRe (Max Planck Society) (submittedVersion)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Keywords
action potential backpropagation, dendritic morphology, dendritic geometry, voltage-gated ion channels, channel density, forward propagation, Purkinje cells, dopaminergic neurons, pyramidal neurons, dendritic compartmentalization, neuron modeling
MeSH terms
Action Potentials, Animals, Computer Simulation, Dendrites, Mathematics, Models, Neurological, Neurons, Potassium Channels, Sodium Channels, Rats

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