Cargando…
Flexible theta sequence compression mediated via phase precessing interneurons
Encoding of behavioral episodes as spike sequences during hippocampal theta oscillations provides a neural substrate for computations on events extended across time and space. However, the mechanisms underlying the numerous and diverse experimentally observed properties of theta sequences remain poo...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245972/ https://www.ncbi.nlm.nih.gov/pubmed/27929374 http://dx.doi.org/10.7554/eLife.20349 |
_version_ | 1782496918416392192 |
---|---|
author | Chadwick, Angus van Rossum, Mark CW Nolan, Matthew F |
author_facet | Chadwick, Angus van Rossum, Mark CW Nolan, Matthew F |
author_sort | Chadwick, Angus |
collection | PubMed |
description | Encoding of behavioral episodes as spike sequences during hippocampal theta oscillations provides a neural substrate for computations on events extended across time and space. However, the mechanisms underlying the numerous and diverse experimentally observed properties of theta sequences remain poorly understood. Here we account for theta sequences using a novel model constrained by the septo-hippocampal circuitry. We show that when spontaneously active interneurons integrate spatial signals and theta frequency pacemaker inputs, they generate phase precessing action potentials that can coordinate theta sequences in place cell populations. We reveal novel constraints on sequence generation, predict cellular properties and neural dynamics that characterize sequence compression, identify circuit organization principles for high capacity sequential representation, and show that theta sequences can be used as substrates for association of conditioned stimuli with recent and upcoming events. Our results suggest mechanisms for flexible sequence compression that are suited to associative learning across an animal’s lifespan. DOI: http://dx.doi.org/10.7554/eLife.20349.001 |
format | Online Article Text |
id | pubmed-5245972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52459722017-01-25 Flexible theta sequence compression mediated via phase precessing interneurons Chadwick, Angus van Rossum, Mark CW Nolan, Matthew F eLife Computational and Systems Biology Encoding of behavioral episodes as spike sequences during hippocampal theta oscillations provides a neural substrate for computations on events extended across time and space. However, the mechanisms underlying the numerous and diverse experimentally observed properties of theta sequences remain poorly understood. Here we account for theta sequences using a novel model constrained by the septo-hippocampal circuitry. We show that when spontaneously active interneurons integrate spatial signals and theta frequency pacemaker inputs, they generate phase precessing action potentials that can coordinate theta sequences in place cell populations. We reveal novel constraints on sequence generation, predict cellular properties and neural dynamics that characterize sequence compression, identify circuit organization principles for high capacity sequential representation, and show that theta sequences can be used as substrates for association of conditioned stimuli with recent and upcoming events. Our results suggest mechanisms for flexible sequence compression that are suited to associative learning across an animal’s lifespan. DOI: http://dx.doi.org/10.7554/eLife.20349.001 eLife Sciences Publications, Ltd 2016-12-08 /pmc/articles/PMC5245972/ /pubmed/27929374 http://dx.doi.org/10.7554/eLife.20349 Text en © 2016, Chadwick et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Chadwick, Angus van Rossum, Mark CW Nolan, Matthew F Flexible theta sequence compression mediated via phase precessing interneurons |
title | Flexible theta sequence compression mediated via phase precessing interneurons |
title_full | Flexible theta sequence compression mediated via phase precessing interneurons |
title_fullStr | Flexible theta sequence compression mediated via phase precessing interneurons |
title_full_unstemmed | Flexible theta sequence compression mediated via phase precessing interneurons |
title_short | Flexible theta sequence compression mediated via phase precessing interneurons |
title_sort | flexible theta sequence compression mediated via phase precessing interneurons |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245972/ https://www.ncbi.nlm.nih.gov/pubmed/27929374 http://dx.doi.org/10.7554/eLife.20349 |
work_keys_str_mv | AT chadwickangus flexiblethetasequencecompressionmediatedviaphaseprecessinginterneurons AT vanrossummarkcw flexiblethetasequencecompressionmediatedviaphaseprecessinginterneurons AT nolanmatthewf flexiblethetasequencecompressionmediatedviaphaseprecessinginterneurons |