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Linking Macroscopic with Microscopic Neuroanatomy Using Synthetic Neuronal Populations

Dendritic morphology has been shown to have a dramatic impact on neuronal function. However, population features such as the inherent variability in dendritic morphology between cells belonging to the same neuronal type are often overlooked when studying computation in neural networks. While detaile...

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Detalles Bibliográficos
Autores principales: Schneider, Calvin J., Cuntz, Hermann, Soltesz, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207466/
https://www.ncbi.nlm.nih.gov/pubmed/25340814
http://dx.doi.org/10.1371/journal.pcbi.1003921
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author Schneider, Calvin J.
Cuntz, Hermann
Soltesz, Ivan
author_facet Schneider, Calvin J.
Cuntz, Hermann
Soltesz, Ivan
author_sort Schneider, Calvin J.
collection PubMed
description Dendritic morphology has been shown to have a dramatic impact on neuronal function. However, population features such as the inherent variability in dendritic morphology between cells belonging to the same neuronal type are often overlooked when studying computation in neural networks. While detailed models for morphology and electrophysiology exist for many types of single neurons, the role of detailed single cell morphology in the population has not been studied quantitatively or computationally. Here we use the structural context of the neural tissue in which dendritic trees exist to drive their generation in silico. We synthesize the entire population of dentate gyrus granule cells, the most numerous cell type in the hippocampus, by growing their dendritic trees within their characteristic dendritic fields bounded by the realistic structural context of (1) the granule cell layer that contains all somata and (2) the molecular layer that contains the dendritic forest. This process enables branching statistics to be linked to larger scale neuroanatomical features. We find large differences in dendritic total length and individual path length measures as a function of location in the dentate gyrus and of somatic depth in the granule cell layer. We also predict the number of unique granule cell dendrites invading a given volume in the molecular layer. This work enables the complete population-level study of morphological properties and provides a framework to develop complex and realistic neural network models.
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spelling pubmed-42074662014-10-27 Linking Macroscopic with Microscopic Neuroanatomy Using Synthetic Neuronal Populations Schneider, Calvin J. Cuntz, Hermann Soltesz, Ivan PLoS Comput Biol Research Article Dendritic morphology has been shown to have a dramatic impact on neuronal function. However, population features such as the inherent variability in dendritic morphology between cells belonging to the same neuronal type are often overlooked when studying computation in neural networks. While detailed models for morphology and electrophysiology exist for many types of single neurons, the role of detailed single cell morphology in the population has not been studied quantitatively or computationally. Here we use the structural context of the neural tissue in which dendritic trees exist to drive their generation in silico. We synthesize the entire population of dentate gyrus granule cells, the most numerous cell type in the hippocampus, by growing their dendritic trees within their characteristic dendritic fields bounded by the realistic structural context of (1) the granule cell layer that contains all somata and (2) the molecular layer that contains the dendritic forest. This process enables branching statistics to be linked to larger scale neuroanatomical features. We find large differences in dendritic total length and individual path length measures as a function of location in the dentate gyrus and of somatic depth in the granule cell layer. We also predict the number of unique granule cell dendrites invading a given volume in the molecular layer. This work enables the complete population-level study of morphological properties and provides a framework to develop complex and realistic neural network models. Public Library of Science 2014-10-23 /pmc/articles/PMC4207466/ /pubmed/25340814 http://dx.doi.org/10.1371/journal.pcbi.1003921 Text en © 2014 Schneider et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Schneider, Calvin J.
Cuntz, Hermann
Soltesz, Ivan
Linking Macroscopic with Microscopic Neuroanatomy Using Synthetic Neuronal Populations
title Linking Macroscopic with Microscopic Neuroanatomy Using Synthetic Neuronal Populations
title_full Linking Macroscopic with Microscopic Neuroanatomy Using Synthetic Neuronal Populations
title_fullStr Linking Macroscopic with Microscopic Neuroanatomy Using Synthetic Neuronal Populations
title_full_unstemmed Linking Macroscopic with Microscopic Neuroanatomy Using Synthetic Neuronal Populations
title_short Linking Macroscopic with Microscopic Neuroanatomy Using Synthetic Neuronal Populations
title_sort linking macroscopic with microscopic neuroanatomy using synthetic neuronal populations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207466/
https://www.ncbi.nlm.nih.gov/pubmed/25340814
http://dx.doi.org/10.1371/journal.pcbi.1003921
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