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Segregation of cortical head direction cell assemblies on alternating theta cycles

High-level cortical systems for spatial navigation, including entorhinal grid cells, critically depend on input from the head direction system. We examined spiking rhythms and modes of synchrony between neurons participating in head direction networks for evidence of internal processing, independent...

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Detalles Bibliográficos
Autores principales: Brandon, Mark P., Bogaard, Andrew R., Schultheiss, Nathan W., Hasselmo, Michael E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3703458/
https://www.ncbi.nlm.nih.gov/pubmed/23603709
http://dx.doi.org/10.1038/nn.3383
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author Brandon, Mark P.
Bogaard, Andrew R.
Schultheiss, Nathan W.
Hasselmo, Michael E.
author_facet Brandon, Mark P.
Bogaard, Andrew R.
Schultheiss, Nathan W.
Hasselmo, Michael E.
author_sort Brandon, Mark P.
collection PubMed
description High-level cortical systems for spatial navigation, including entorhinal grid cells, critically depend on input from the head direction system. We examined spiking rhythms and modes of synchrony between neurons participating in head direction networks for evidence of internal processing, independent of direct sensory drive, which may be important for grid cell function. We demonstrate that head direction networks of rats are segregated into at least two populations of neurons firing on alternate theta cycles (theta cycle skipping) with fixed synchronous or anti-synchronous relationships. Pairs of anti-synchronous theta cycle skipping neurons exhibited larger differences in head direction tuning with a minimum difference of 40 degrees of head direction. Septal inactivation preserved the head direction signal but eliminated theta cycle skipping of head direction cells and grid cell spatial periodicity. We propose that internal mechanisms underlying cycle skipping in head direction networks may be critical for downstream spatial computation by grid cells.
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spelling pubmed-37034582013-12-01 Segregation of cortical head direction cell assemblies on alternating theta cycles Brandon, Mark P. Bogaard, Andrew R. Schultheiss, Nathan W. Hasselmo, Michael E. Nat Neurosci Article High-level cortical systems for spatial navigation, including entorhinal grid cells, critically depend on input from the head direction system. We examined spiking rhythms and modes of synchrony between neurons participating in head direction networks for evidence of internal processing, independent of direct sensory drive, which may be important for grid cell function. We demonstrate that head direction networks of rats are segregated into at least two populations of neurons firing on alternate theta cycles (theta cycle skipping) with fixed synchronous or anti-synchronous relationships. Pairs of anti-synchronous theta cycle skipping neurons exhibited larger differences in head direction tuning with a minimum difference of 40 degrees of head direction. Septal inactivation preserved the head direction signal but eliminated theta cycle skipping of head direction cells and grid cell spatial periodicity. We propose that internal mechanisms underlying cycle skipping in head direction networks may be critical for downstream spatial computation by grid cells. 2013-04-21 2013-06 /pmc/articles/PMC3703458/ /pubmed/23603709 http://dx.doi.org/10.1038/nn.3383 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Brandon, Mark P.
Bogaard, Andrew R.
Schultheiss, Nathan W.
Hasselmo, Michael E.
Segregation of cortical head direction cell assemblies on alternating theta cycles
title Segregation of cortical head direction cell assemblies on alternating theta cycles
title_full Segregation of cortical head direction cell assemblies on alternating theta cycles
title_fullStr Segregation of cortical head direction cell assemblies on alternating theta cycles
title_full_unstemmed Segregation of cortical head direction cell assemblies on alternating theta cycles
title_short Segregation of cortical head direction cell assemblies on alternating theta cycles
title_sort segregation of cortical head direction cell assemblies on alternating theta cycles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3703458/
https://www.ncbi.nlm.nih.gov/pubmed/23603709
http://dx.doi.org/10.1038/nn.3383
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