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Cortical interneurons that specialize in disinhibitory control
In the mammalian cerebral cortex, the diversity of interneuronal subtypes underlies a division of labor subserving distinct modes of inhibitory control(1–7). A unique mode of inhibitory control may be provided by inhibitory neurons that specifically suppress the firing of other inhibitory neurons. S...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017628/ https://www.ncbi.nlm.nih.gov/pubmed/24097352 http://dx.doi.org/10.1038/nature12676 |
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author | Pi, Hyun-Jae Hangya, Balázs Kvitsiani, Duda Sanders, Joshua I. Huang, Z. Josh Kepecs, Adam |
author_facet | Pi, Hyun-Jae Hangya, Balázs Kvitsiani, Duda Sanders, Joshua I. Huang, Z. Josh Kepecs, Adam |
author_sort | Pi, Hyun-Jae |
collection | PubMed |
description | In the mammalian cerebral cortex, the diversity of interneuronal subtypes underlies a division of labor subserving distinct modes of inhibitory control(1–7). A unique mode of inhibitory control may be provided by inhibitory neurons that specifically suppress the firing of other inhibitory neurons. Such disinhibition could lead to the selective amplification of local processing and serve the important computational functions of gating and gain modulation(8,9). Although several interneuron populations are known to target other interneurons to varying degrees(10–15), little is known about interneurons specializing in disinhibition and their in vivo function. Here we show that a class of interneurons that express vasoactive intestinal polypeptide (VIP) mediates disinhibitory control in multiple areas of neocortex and is recruited by reinforcement signals. By combining optogenetic activation with single cell recordings, we examined the functional role of VIP interneurons in awake mice, and investigated the underlying circuit mechanisms in vitro in auditory and medial prefrontal cortices. We identified a basic disinhibitory circuit module in which activation of VIP interneurons transiently suppresses primarily somatostatin- and a fraction of parvalbumin-expressing inhibitory interneurons that specialize in the control of the input and output of principal cells, respectively(3,6,16,17). During the performance of an auditory discrimination task, reinforcement signals (reward and punishment) strongly and uniformly activated VIP neurons in auditory cortex, and in turn VIP recruitment increased the gain of a functional subpopulation of principal neurons. These results reveal a specific cell-type and microcircuit underlying disinhibitory control in cortex and demonstrate that it is activated under specific behavioural conditions. |
format | Online Article Text |
id | pubmed-4017628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-40176282014-05-28 Cortical interneurons that specialize in disinhibitory control Pi, Hyun-Jae Hangya, Balázs Kvitsiani, Duda Sanders, Joshua I. Huang, Z. Josh Kepecs, Adam Nature Article In the mammalian cerebral cortex, the diversity of interneuronal subtypes underlies a division of labor subserving distinct modes of inhibitory control(1–7). A unique mode of inhibitory control may be provided by inhibitory neurons that specifically suppress the firing of other inhibitory neurons. Such disinhibition could lead to the selective amplification of local processing and serve the important computational functions of gating and gain modulation(8,9). Although several interneuron populations are known to target other interneurons to varying degrees(10–15), little is known about interneurons specializing in disinhibition and their in vivo function. Here we show that a class of interneurons that express vasoactive intestinal polypeptide (VIP) mediates disinhibitory control in multiple areas of neocortex and is recruited by reinforcement signals. By combining optogenetic activation with single cell recordings, we examined the functional role of VIP interneurons in awake mice, and investigated the underlying circuit mechanisms in vitro in auditory and medial prefrontal cortices. We identified a basic disinhibitory circuit module in which activation of VIP interneurons transiently suppresses primarily somatostatin- and a fraction of parvalbumin-expressing inhibitory interneurons that specialize in the control of the input and output of principal cells, respectively(3,6,16,17). During the performance of an auditory discrimination task, reinforcement signals (reward and punishment) strongly and uniformly activated VIP neurons in auditory cortex, and in turn VIP recruitment increased the gain of a functional subpopulation of principal neurons. These results reveal a specific cell-type and microcircuit underlying disinhibitory control in cortex and demonstrate that it is activated under specific behavioural conditions. 2013-10-06 2013-11-28 /pmc/articles/PMC4017628/ /pubmed/24097352 http://dx.doi.org/10.1038/nature12676 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 Pi, Hyun-Jae Hangya, Balázs Kvitsiani, Duda Sanders, Joshua I. Huang, Z. Josh Kepecs, Adam Cortical interneurons that specialize in disinhibitory control |
title | Cortical interneurons that specialize in disinhibitory control |
title_full | Cortical interneurons that specialize in disinhibitory control |
title_fullStr | Cortical interneurons that specialize in disinhibitory control |
title_full_unstemmed | Cortical interneurons that specialize in disinhibitory control |
title_short | Cortical interneurons that specialize in disinhibitory control |
title_sort | cortical interneurons that specialize in disinhibitory control |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017628/ https://www.ncbi.nlm.nih.gov/pubmed/24097352 http://dx.doi.org/10.1038/nature12676 |
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