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Spatially resolved dendritic integration: towards a functional classification of neurons
The vast tree-like dendritic structure of neurons allows them to receive and integrate input from many neurons. A wide variety of neuronal morphologies exist, however, their role in dendritic integration, and how it shapes the response of the neuron, is not yet fully understood. Here, we study the e...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694565/ https://www.ncbi.nlm.nih.gov/pubmed/33282551 http://dx.doi.org/10.7717/peerj.10250 |
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author | Kirch, Christoph Gollo, Leonardo L. |
author_facet | Kirch, Christoph Gollo, Leonardo L. |
author_sort | Kirch, Christoph |
collection | PubMed |
description | The vast tree-like dendritic structure of neurons allows them to receive and integrate input from many neurons. A wide variety of neuronal morphologies exist, however, their role in dendritic integration, and how it shapes the response of the neuron, is not yet fully understood. Here, we study the evolution and interactions of dendritic spikes in excitable neurons with complex real branch structures. We focus on dozens of digitally reconstructed illustrative neurons from the online repository NeuroMorpho.org, which contains over 130,000 neurons. Yet, our methods can be promptly extended to any other neuron. This approach allows us to estimate and map specific and heterogeneous patterns of activity observed across extensive dendritic trees with thousands of compartments. We propose a classification of neurons based on the location of the soma (centrality) and the number of branches connected to the soma. These are key topological factors in determining the neuron’s energy consumption, firing rate, and the dynamic range, which quantifies the range in synaptic input rate that can be reliably encoded by the neuron’s firing rate. Moreover, we find that bifurcations, the structural building blocks of complex dendrites, play a major role in increasing the dynamic range of neurons. Our results provide a better understanding of the effects of neuronal morphology in the diversity of neuronal dynamics and function. |
format | Online Article Text |
id | pubmed-7694565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76945652020-12-04 Spatially resolved dendritic integration: towards a functional classification of neurons Kirch, Christoph Gollo, Leonardo L. PeerJ Computational Biology The vast tree-like dendritic structure of neurons allows them to receive and integrate input from many neurons. A wide variety of neuronal morphologies exist, however, their role in dendritic integration, and how it shapes the response of the neuron, is not yet fully understood. Here, we study the evolution and interactions of dendritic spikes in excitable neurons with complex real branch structures. We focus on dozens of digitally reconstructed illustrative neurons from the online repository NeuroMorpho.org, which contains over 130,000 neurons. Yet, our methods can be promptly extended to any other neuron. This approach allows us to estimate and map specific and heterogeneous patterns of activity observed across extensive dendritic trees with thousands of compartments. We propose a classification of neurons based on the location of the soma (centrality) and the number of branches connected to the soma. These are key topological factors in determining the neuron’s energy consumption, firing rate, and the dynamic range, which quantifies the range in synaptic input rate that can be reliably encoded by the neuron’s firing rate. Moreover, we find that bifurcations, the structural building blocks of complex dendrites, play a major role in increasing the dynamic range of neurons. Our results provide a better understanding of the effects of neuronal morphology in the diversity of neuronal dynamics and function. PeerJ Inc. 2020-11-24 /pmc/articles/PMC7694565/ /pubmed/33282551 http://dx.doi.org/10.7717/peerj.10250 Text en © 2020 Kirch and Gollo https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Computational Biology Kirch, Christoph Gollo, Leonardo L. Spatially resolved dendritic integration: towards a functional classification of neurons |
title | Spatially resolved dendritic integration: towards a functional classification of neurons |
title_full | Spatially resolved dendritic integration: towards a functional classification of neurons |
title_fullStr | Spatially resolved dendritic integration: towards a functional classification of neurons |
title_full_unstemmed | Spatially resolved dendritic integration: towards a functional classification of neurons |
title_short | Spatially resolved dendritic integration: towards a functional classification of neurons |
title_sort | spatially resolved dendritic integration: towards a functional classification of neurons |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694565/ https://www.ncbi.nlm.nih.gov/pubmed/33282551 http://dx.doi.org/10.7717/peerj.10250 |
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