Cargando…

Communication and wiring in the cortical connectome

In cerebral cortex, the huge mass of axonal wiring that carries information between near and distant neurons is thought to provide the neural substrate for cognitive and perceptual function. The goal of mapping the connectivity of cortical axons at different spatial scales, the cortical connectome,...

Descripción completa

Detalles Bibliográficos
Autores principales: Budd, Julian M. L., Kisvárday, Zoltán F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472565/
https://www.ncbi.nlm.nih.gov/pubmed/23087619
http://dx.doi.org/10.3389/fnana.2012.00042
_version_ 1782246620232941568
author Budd, Julian M. L.
Kisvárday, Zoltán F.
author_facet Budd, Julian M. L.
Kisvárday, Zoltán F.
author_sort Budd, Julian M. L.
collection PubMed
description In cerebral cortex, the huge mass of axonal wiring that carries information between near and distant neurons is thought to provide the neural substrate for cognitive and perceptual function. The goal of mapping the connectivity of cortical axons at different spatial scales, the cortical connectome, is to trace the paths of information flow in cerebral cortex. To appreciate the relationship between the connectome and cortical function, we need to discover the nature and purpose of the wiring principles underlying cortical connectivity. A popular explanation has been that axonal length is strictly minimized both within and between cortical regions. In contrast, we have hypothesized the existence of a multi-scale principle of cortical wiring where to optimize communication there is a trade-off between spatial (construction) and temporal (routing) costs. Here, using recent evidence concerning cortical spatial networks we critically evaluate this hypothesis at neuron, local circuit, and pathway scales. We report three main conclusions. First, the axonal and dendritic arbor morphology of single neocortical neurons may be governed by a similar wiring principle, one that balances the conservation of cellular material and conduction delay. Second, the same principle may be observed for fiber tracts connecting cortical regions. Third, the absence of sufficient local circuit data currently prohibits any meaningful assessment of the hypothesis at this scale of cortical organization. To avoid neglecting neuron and microcircuit levels of cortical organization, the connectome framework should incorporate more morphological description. In addition, structural analyses of temporal cost for cortical circuits should take account of both axonal conduction and neuronal integration delays, which appear mostly of the same order of magnitude. We conclude the hypothesized trade-off between spatial and temporal costs may potentially offer a powerful explanation for cortical wiring patterns.
format Online
Article
Text
id pubmed-3472565
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-34725652012-10-19 Communication and wiring in the cortical connectome Budd, Julian M. L. Kisvárday, Zoltán F. Front Neuroanat Neuroscience In cerebral cortex, the huge mass of axonal wiring that carries information between near and distant neurons is thought to provide the neural substrate for cognitive and perceptual function. The goal of mapping the connectivity of cortical axons at different spatial scales, the cortical connectome, is to trace the paths of information flow in cerebral cortex. To appreciate the relationship between the connectome and cortical function, we need to discover the nature and purpose of the wiring principles underlying cortical connectivity. A popular explanation has been that axonal length is strictly minimized both within and between cortical regions. In contrast, we have hypothesized the existence of a multi-scale principle of cortical wiring where to optimize communication there is a trade-off between spatial (construction) and temporal (routing) costs. Here, using recent evidence concerning cortical spatial networks we critically evaluate this hypothesis at neuron, local circuit, and pathway scales. We report three main conclusions. First, the axonal and dendritic arbor morphology of single neocortical neurons may be governed by a similar wiring principle, one that balances the conservation of cellular material and conduction delay. Second, the same principle may be observed for fiber tracts connecting cortical regions. Third, the absence of sufficient local circuit data currently prohibits any meaningful assessment of the hypothesis at this scale of cortical organization. To avoid neglecting neuron and microcircuit levels of cortical organization, the connectome framework should incorporate more morphological description. In addition, structural analyses of temporal cost for cortical circuits should take account of both axonal conduction and neuronal integration delays, which appear mostly of the same order of magnitude. We conclude the hypothesized trade-off between spatial and temporal costs may potentially offer a powerful explanation for cortical wiring patterns. Frontiers Media S.A. 2012-10-16 /pmc/articles/PMC3472565/ /pubmed/23087619 http://dx.doi.org/10.3389/fnana.2012.00042 Text en Copyright © 2012 Budd and Kisvárday. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Budd, Julian M. L.
Kisvárday, Zoltán F.
Communication and wiring in the cortical connectome
title Communication and wiring in the cortical connectome
title_full Communication and wiring in the cortical connectome
title_fullStr Communication and wiring in the cortical connectome
title_full_unstemmed Communication and wiring in the cortical connectome
title_short Communication and wiring in the cortical connectome
title_sort communication and wiring in the cortical connectome
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472565/
https://www.ncbi.nlm.nih.gov/pubmed/23087619
http://dx.doi.org/10.3389/fnana.2012.00042
work_keys_str_mv AT buddjulianml communicationandwiringinthecorticalconnectome
AT kisvardayzoltanf communicationandwiringinthecorticalconnectome