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Activity-dependent tuning of intrinsic excitability in mouse and human neurogliaform cells
The ability to modulate the efficacy of synaptic communication between neurons constitutes an essential property critical for normal brain function. Animal models have proved invaluable in revealing a wealth of diverse cellular mechanisms underlying varied plasticity modes. However, to what extent t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299336/ https://www.ncbi.nlm.nih.gov/pubmed/32496194 http://dx.doi.org/10.7554/eLife.57571 |
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author | Chittajallu, Ramesh Auville, Kurt Mahadevan, Vivek Lai, Mandy Hunt, Steven Calvigioni, Daniela Pelkey, Kenneth A Zaghloul, Kareem A McBain, Chris J |
author_facet | Chittajallu, Ramesh Auville, Kurt Mahadevan, Vivek Lai, Mandy Hunt, Steven Calvigioni, Daniela Pelkey, Kenneth A Zaghloul, Kareem A McBain, Chris J |
author_sort | Chittajallu, Ramesh |
collection | PubMed |
description | The ability to modulate the efficacy of synaptic communication between neurons constitutes an essential property critical for normal brain function. Animal models have proved invaluable in revealing a wealth of diverse cellular mechanisms underlying varied plasticity modes. However, to what extent these processes are mirrored in humans is largely uncharted thus questioning their relevance in human circuit function. In this study, we focus on neurogliaform cells, that possess specialized physiological features enabling them to impart a widespread inhibitory influence on neural activity. We demonstrate that this prominent neuronal subtype, embedded in both mouse and human neural circuits, undergo remarkably similar activity-dependent modulation manifesting as epochs of enhanced intrinsic excitability. In principle, these evolutionary conserved plasticity routes likely tune the extent of neurogliaform cell mediated inhibition thus constituting canonical circuit mechanisms underlying human cognitive processing and behavior. |
format | Online Article Text |
id | pubmed-7299336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-72993362020-06-18 Activity-dependent tuning of intrinsic excitability in mouse and human neurogliaform cells Chittajallu, Ramesh Auville, Kurt Mahadevan, Vivek Lai, Mandy Hunt, Steven Calvigioni, Daniela Pelkey, Kenneth A Zaghloul, Kareem A McBain, Chris J eLife Neuroscience The ability to modulate the efficacy of synaptic communication between neurons constitutes an essential property critical for normal brain function. Animal models have proved invaluable in revealing a wealth of diverse cellular mechanisms underlying varied plasticity modes. However, to what extent these processes are mirrored in humans is largely uncharted thus questioning their relevance in human circuit function. In this study, we focus on neurogliaform cells, that possess specialized physiological features enabling them to impart a widespread inhibitory influence on neural activity. We demonstrate that this prominent neuronal subtype, embedded in both mouse and human neural circuits, undergo remarkably similar activity-dependent modulation manifesting as epochs of enhanced intrinsic excitability. In principle, these evolutionary conserved plasticity routes likely tune the extent of neurogliaform cell mediated inhibition thus constituting canonical circuit mechanisms underlying human cognitive processing and behavior. eLife Sciences Publications, Ltd 2020-06-04 /pmc/articles/PMC7299336/ /pubmed/32496194 http://dx.doi.org/10.7554/eLife.57571 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (https://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Neuroscience Chittajallu, Ramesh Auville, Kurt Mahadevan, Vivek Lai, Mandy Hunt, Steven Calvigioni, Daniela Pelkey, Kenneth A Zaghloul, Kareem A McBain, Chris J Activity-dependent tuning of intrinsic excitability in mouse and human neurogliaform cells |
title | Activity-dependent tuning of intrinsic excitability in mouse and human neurogliaform cells |
title_full | Activity-dependent tuning of intrinsic excitability in mouse and human neurogliaform cells |
title_fullStr | Activity-dependent tuning of intrinsic excitability in mouse and human neurogliaform cells |
title_full_unstemmed | Activity-dependent tuning of intrinsic excitability in mouse and human neurogliaform cells |
title_short | Activity-dependent tuning of intrinsic excitability in mouse and human neurogliaform cells |
title_sort | activity-dependent tuning of intrinsic excitability in mouse and human neurogliaform cells |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299336/ https://www.ncbi.nlm.nih.gov/pubmed/32496194 http://dx.doi.org/10.7554/eLife.57571 |
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