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VIP interneurons regulate cortical size tuning and visual perception
Local cortical circuit function is regulated by diverse populations of GABAergic interneurons with distinct properties and extensive interconnectivity. Inhibitory-to-inhibitory interactions between interneuron populations may play key roles in shaping circuit operation according to behavioral contex...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168200/ https://www.ncbi.nlm.nih.gov/pubmed/37162871 http://dx.doi.org/10.1101/2023.03.14.532664 |
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author | Ferguson, Katie A. Salameh, Jenna Alba, Christopher Selwyn, Hannah Barnes, Clayton Lohani, Sweyta Cardin, Jessica A. |
author_facet | Ferguson, Katie A. Salameh, Jenna Alba, Christopher Selwyn, Hannah Barnes, Clayton Lohani, Sweyta Cardin, Jessica A. |
author_sort | Ferguson, Katie A. |
collection | PubMed |
description | Local cortical circuit function is regulated by diverse populations of GABAergic interneurons with distinct properties and extensive interconnectivity. Inhibitory-to-inhibitory interactions between interneuron populations may play key roles in shaping circuit operation according to behavioral context. A specialized population of GABAergic interneurons that co-express vasoactive intestinal peptide (VIP-INs) are activated during arousal and locomotion and innervate other local interneurons and pyramidal neurons. Although modulation of VIP-IN activity by behavioral state has been extensively studied, their role in regulating information processing and selectivity is less well understood. Using a combination of cellular imaging, short- and long-term manipulation, and perceptual behavior, we examined the impact of VIP-INs on their synaptic target populations in the primary visual cortex of awake behaving mice. We find that loss of VIP-IN activity alters the behavioral state-dependent modulation of somatostatin-expressing interneurons (SST-INs) but not pyramidal neurons (PNs). In contrast, reduced VIP-IN activity disrupts visual feature selectivity for stimulus size in both populations. Inhibitory-to-inhibitory interactions thus directly shape the selectivity of GABAergic interneurons for sensory stimuli. Moreover, the impact of VIP-IN activity on perceptual behavior varies with visual context and is more acute for small than large visual cues. VIP-INs thus contribute to both state-dependent modulation of cortical circuit activity and sensory context-dependent perceptual performance. |
format | Online Article Text |
id | pubmed-10168200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101682002023-05-10 VIP interneurons regulate cortical size tuning and visual perception Ferguson, Katie A. Salameh, Jenna Alba, Christopher Selwyn, Hannah Barnes, Clayton Lohani, Sweyta Cardin, Jessica A. bioRxiv Article Local cortical circuit function is regulated by diverse populations of GABAergic interneurons with distinct properties and extensive interconnectivity. Inhibitory-to-inhibitory interactions between interneuron populations may play key roles in shaping circuit operation according to behavioral context. A specialized population of GABAergic interneurons that co-express vasoactive intestinal peptide (VIP-INs) are activated during arousal and locomotion and innervate other local interneurons and pyramidal neurons. Although modulation of VIP-IN activity by behavioral state has been extensively studied, their role in regulating information processing and selectivity is less well understood. Using a combination of cellular imaging, short- and long-term manipulation, and perceptual behavior, we examined the impact of VIP-INs on their synaptic target populations in the primary visual cortex of awake behaving mice. We find that loss of VIP-IN activity alters the behavioral state-dependent modulation of somatostatin-expressing interneurons (SST-INs) but not pyramidal neurons (PNs). In contrast, reduced VIP-IN activity disrupts visual feature selectivity for stimulus size in both populations. Inhibitory-to-inhibitory interactions thus directly shape the selectivity of GABAergic interneurons for sensory stimuli. Moreover, the impact of VIP-IN activity on perceptual behavior varies with visual context and is more acute for small than large visual cues. VIP-INs thus contribute to both state-dependent modulation of cortical circuit activity and sensory context-dependent perceptual performance. Cold Spring Harbor Laboratory 2023-04-28 /pmc/articles/PMC10168200/ /pubmed/37162871 http://dx.doi.org/10.1101/2023.03.14.532664 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Ferguson, Katie A. Salameh, Jenna Alba, Christopher Selwyn, Hannah Barnes, Clayton Lohani, Sweyta Cardin, Jessica A. VIP interneurons regulate cortical size tuning and visual perception |
title | VIP interneurons regulate cortical size tuning and visual perception |
title_full | VIP interneurons regulate cortical size tuning and visual perception |
title_fullStr | VIP interneurons regulate cortical size tuning and visual perception |
title_full_unstemmed | VIP interneurons regulate cortical size tuning and visual perception |
title_short | VIP interneurons regulate cortical size tuning and visual perception |
title_sort | vip interneurons regulate cortical size tuning and visual perception |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168200/ https://www.ncbi.nlm.nih.gov/pubmed/37162871 http://dx.doi.org/10.1101/2023.03.14.532664 |
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