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Developmental divergence of sensory stimulus representation in cortical interneurons
Vasocative-intestinal-peptide (VIP(+)) and somatostatin (SST(+)) interneurons are involved in modulating barrel cortex activity and perception during active whisking. Here we identify a developmental transition point of structural and functional rearrangements onto these interneurons around the star...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7661508/ https://www.ncbi.nlm.nih.gov/pubmed/33184269 http://dx.doi.org/10.1038/s41467-020-19427-z |
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author | Kastli, Rahel Vighagen, Rasmus van der Bourg, Alexander Argunsah, Ali Özgür Iqbal, Asim Voigt, Fabian F. Kirschenbaum, Daniel Aguzzi, Adriano Helmchen, Fritjof Karayannis, Theofanis |
author_facet | Kastli, Rahel Vighagen, Rasmus van der Bourg, Alexander Argunsah, Ali Özgür Iqbal, Asim Voigt, Fabian F. Kirschenbaum, Daniel Aguzzi, Adriano Helmchen, Fritjof Karayannis, Theofanis |
author_sort | Kastli, Rahel |
collection | PubMed |
description | Vasocative-intestinal-peptide (VIP(+)) and somatostatin (SST(+)) interneurons are involved in modulating barrel cortex activity and perception during active whisking. Here we identify a developmental transition point of structural and functional rearrangements onto these interneurons around the start of active sensation at P14. Using in vivo two-photon Ca(2+) imaging, we find that before P14, both interneuron types respond stronger to a multi-whisker stimulus, whereas after P14 their responses diverge, with VIP(+) cells losing their multi-whisker preference and SST(+) neurons enhancing theirs. Additionally, we find that Ca(2+) signaling dynamics increase in precision as the cells and network mature. Rabies virus tracings followed by tissue clearing, as well as photostimulation-coupled electrophysiology reveal that SST(+) cells receive higher cross-barrel inputs compared to VIP(+) neurons at both time points. In addition, whereas prior to P14 both cell types receive direct input from the sensory thalamus, after P14 VIP(+) cells show reduced inputs and SST(+) cells largely shift to motor-related thalamic nuclei. |
format | Online Article Text |
id | pubmed-7661508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76615082020-11-17 Developmental divergence of sensory stimulus representation in cortical interneurons Kastli, Rahel Vighagen, Rasmus van der Bourg, Alexander Argunsah, Ali Özgür Iqbal, Asim Voigt, Fabian F. Kirschenbaum, Daniel Aguzzi, Adriano Helmchen, Fritjof Karayannis, Theofanis Nat Commun Article Vasocative-intestinal-peptide (VIP(+)) and somatostatin (SST(+)) interneurons are involved in modulating barrel cortex activity and perception during active whisking. Here we identify a developmental transition point of structural and functional rearrangements onto these interneurons around the start of active sensation at P14. Using in vivo two-photon Ca(2+) imaging, we find that before P14, both interneuron types respond stronger to a multi-whisker stimulus, whereas after P14 their responses diverge, with VIP(+) cells losing their multi-whisker preference and SST(+) neurons enhancing theirs. Additionally, we find that Ca(2+) signaling dynamics increase in precision as the cells and network mature. Rabies virus tracings followed by tissue clearing, as well as photostimulation-coupled electrophysiology reveal that SST(+) cells receive higher cross-barrel inputs compared to VIP(+) neurons at both time points. In addition, whereas prior to P14 both cell types receive direct input from the sensory thalamus, after P14 VIP(+) cells show reduced inputs and SST(+) cells largely shift to motor-related thalamic nuclei. Nature Publishing Group UK 2020-11-12 /pmc/articles/PMC7661508/ /pubmed/33184269 http://dx.doi.org/10.1038/s41467-020-19427-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kastli, Rahel Vighagen, Rasmus van der Bourg, Alexander Argunsah, Ali Özgür Iqbal, Asim Voigt, Fabian F. Kirschenbaum, Daniel Aguzzi, Adriano Helmchen, Fritjof Karayannis, Theofanis Developmental divergence of sensory stimulus representation in cortical interneurons |
title | Developmental divergence of sensory stimulus representation in cortical interneurons |
title_full | Developmental divergence of sensory stimulus representation in cortical interneurons |
title_fullStr | Developmental divergence of sensory stimulus representation in cortical interneurons |
title_full_unstemmed | Developmental divergence of sensory stimulus representation in cortical interneurons |
title_short | Developmental divergence of sensory stimulus representation in cortical interneurons |
title_sort | developmental divergence of sensory stimulus representation in cortical interneurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7661508/ https://www.ncbi.nlm.nih.gov/pubmed/33184269 http://dx.doi.org/10.1038/s41467-020-19427-z |
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