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Distinct neuronal populations contribute to trace conditioning and extinction learning in the hippocampal CA1

Trace conditioning and extinction learning depend on the hippocampus, but it remains unclear how neural activity in the hippocampus is modulated during these two different behavioral processes. To explore this question, we performed calcium imaging from a large number of individual CA1 neurons durin...

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Autores principales: Mount, Rebecca A, Sridhar, Sudiksha, Hansen, Kyle R, Mohammed, Ali I, Abdulkerim, Moona, Kessel, Robb, Nazer, Bobak, Gritton, Howard J, Han, Xue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8064758/
https://www.ncbi.nlm.nih.gov/pubmed/33843589
http://dx.doi.org/10.7554/eLife.56491
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author Mount, Rebecca A
Sridhar, Sudiksha
Hansen, Kyle R
Mohammed, Ali I
Abdulkerim, Moona
Kessel, Robb
Nazer, Bobak
Gritton, Howard J
Han, Xue
author_facet Mount, Rebecca A
Sridhar, Sudiksha
Hansen, Kyle R
Mohammed, Ali I
Abdulkerim, Moona
Kessel, Robb
Nazer, Bobak
Gritton, Howard J
Han, Xue
author_sort Mount, Rebecca A
collection PubMed
description Trace conditioning and extinction learning depend on the hippocampus, but it remains unclear how neural activity in the hippocampus is modulated during these two different behavioral processes. To explore this question, we performed calcium imaging from a large number of individual CA1 neurons during both trace eye-blink conditioning and subsequent extinction learning in mice. Our findings reveal that distinct populations of CA1 cells contribute to trace conditioned learning versus extinction learning, as learning emerges. Furthermore, we examined network connectivity by calculating co-activity between CA1 neuron pairs and found that CA1 network connectivity patterns also differ between conditioning and extinction, even though the overall connectivity density remains constant. Together, our results demonstrate that distinct populations of hippocampal CA1 neurons, forming different sub-networks with unique connectivity patterns, encode different aspects of learning.
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spelling pubmed-80647582021-04-29 Distinct neuronal populations contribute to trace conditioning and extinction learning in the hippocampal CA1 Mount, Rebecca A Sridhar, Sudiksha Hansen, Kyle R Mohammed, Ali I Abdulkerim, Moona Kessel, Robb Nazer, Bobak Gritton, Howard J Han, Xue eLife Neuroscience Trace conditioning and extinction learning depend on the hippocampus, but it remains unclear how neural activity in the hippocampus is modulated during these two different behavioral processes. To explore this question, we performed calcium imaging from a large number of individual CA1 neurons during both trace eye-blink conditioning and subsequent extinction learning in mice. Our findings reveal that distinct populations of CA1 cells contribute to trace conditioned learning versus extinction learning, as learning emerges. Furthermore, we examined network connectivity by calculating co-activity between CA1 neuron pairs and found that CA1 network connectivity patterns also differ between conditioning and extinction, even though the overall connectivity density remains constant. Together, our results demonstrate that distinct populations of hippocampal CA1 neurons, forming different sub-networks with unique connectivity patterns, encode different aspects of learning. eLife Sciences Publications, Ltd 2021-04-12 /pmc/articles/PMC8064758/ /pubmed/33843589 http://dx.doi.org/10.7554/eLife.56491 Text en © 2021, Mount 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 Neuroscience
Mount, Rebecca A
Sridhar, Sudiksha
Hansen, Kyle R
Mohammed, Ali I
Abdulkerim, Moona
Kessel, Robb
Nazer, Bobak
Gritton, Howard J
Han, Xue
Distinct neuronal populations contribute to trace conditioning and extinction learning in the hippocampal CA1
title Distinct neuronal populations contribute to trace conditioning and extinction learning in the hippocampal CA1
title_full Distinct neuronal populations contribute to trace conditioning and extinction learning in the hippocampal CA1
title_fullStr Distinct neuronal populations contribute to trace conditioning and extinction learning in the hippocampal CA1
title_full_unstemmed Distinct neuronal populations contribute to trace conditioning and extinction learning in the hippocampal CA1
title_short Distinct neuronal populations contribute to trace conditioning and extinction learning in the hippocampal CA1
title_sort distinct neuronal populations contribute to trace conditioning and extinction learning in the hippocampal ca1
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8064758/
https://www.ncbi.nlm.nih.gov/pubmed/33843589
http://dx.doi.org/10.7554/eLife.56491
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