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Apical length governs computational diversity of layer 5 pyramidal neurons

Anatomical similarity across the neocortex has led to the common assumption that the circuitry is modular and performs stereotyped computations. Layer 5 pyramidal neurons (L5PNs) in particular are thought to be central to cortical computation because of their extensive arborisation and nonlinear den...

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Detalles Bibliográficos
Autores principales: Galloni, Alessandro R, Laffere, Aeron, Rancz, Ede
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334021/
https://www.ncbi.nlm.nih.gov/pubmed/32463356
http://dx.doi.org/10.7554/eLife.55761
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author Galloni, Alessandro R
Laffere, Aeron
Rancz, Ede
author_facet Galloni, Alessandro R
Laffere, Aeron
Rancz, Ede
author_sort Galloni, Alessandro R
collection PubMed
description Anatomical similarity across the neocortex has led to the common assumption that the circuitry is modular and performs stereotyped computations. Layer 5 pyramidal neurons (L5PNs) in particular are thought to be central to cortical computation because of their extensive arborisation and nonlinear dendritic operations. Here, we demonstrate that computations associated with dendritic Ca(2+) plateaus in mouse L5PNs vary substantially between the primary and secondary visual cortices. L5PNs in the secondary visual cortex show reduced dendritic excitability and smaller propensity for burst firing. This reduced excitability is correlated with shorter apical dendrites. Using numerical modelling, we uncover a universal principle underlying the influence of apical length on dendritic backpropagation and excitability, based on a Na(+) channel-dependent broadening of backpropagating action potentials. In summary, we provide new insights into the modulation of dendritic excitability by apical dendrite length and show that the operational repertoire of L5PNs is not universal throughout the brain.
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spelling pubmed-73340212020-07-13 Apical length governs computational diversity of layer 5 pyramidal neurons Galloni, Alessandro R Laffere, Aeron Rancz, Ede eLife Neuroscience Anatomical similarity across the neocortex has led to the common assumption that the circuitry is modular and performs stereotyped computations. Layer 5 pyramidal neurons (L5PNs) in particular are thought to be central to cortical computation because of their extensive arborisation and nonlinear dendritic operations. Here, we demonstrate that computations associated with dendritic Ca(2+) plateaus in mouse L5PNs vary substantially between the primary and secondary visual cortices. L5PNs in the secondary visual cortex show reduced dendritic excitability and smaller propensity for burst firing. This reduced excitability is correlated with shorter apical dendrites. Using numerical modelling, we uncover a universal principle underlying the influence of apical length on dendritic backpropagation and excitability, based on a Na(+) channel-dependent broadening of backpropagating action potentials. In summary, we provide new insights into the modulation of dendritic excitability by apical dendrite length and show that the operational repertoire of L5PNs is not universal throughout the brain. eLife Sciences Publications, Ltd 2020-05-28 /pmc/articles/PMC7334021/ /pubmed/32463356 http://dx.doi.org/10.7554/eLife.55761 Text en © 2020, Galloni et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Galloni, Alessandro R
Laffere, Aeron
Rancz, Ede
Apical length governs computational diversity of layer 5 pyramidal neurons
title Apical length governs computational diversity of layer 5 pyramidal neurons
title_full Apical length governs computational diversity of layer 5 pyramidal neurons
title_fullStr Apical length governs computational diversity of layer 5 pyramidal neurons
title_full_unstemmed Apical length governs computational diversity of layer 5 pyramidal neurons
title_short Apical length governs computational diversity of layer 5 pyramidal neurons
title_sort apical length governs computational diversity of layer 5 pyramidal neurons
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334021/
https://www.ncbi.nlm.nih.gov/pubmed/32463356
http://dx.doi.org/10.7554/eLife.55761
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