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Targeting barrel field spiny stellate cells using a vesicular monoaminergic transporter 2-Cre mouse line

Rodent primary somatosensory cortex (S1) is organized in defined layers, where layer IV serves as the main target for thalamocortical projections. Serotoninergic signaling is important for the organization of thalamocortical projections and consequently proper barrel field development in rodents, an...

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Autores principales: Freitag, Fabio B., Ahemaiti, Aikeremu, Weman, Hannah M., Ambroz, Katharina, Lagerström, Malin C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864935/
https://www.ncbi.nlm.nih.gov/pubmed/33547358
http://dx.doi.org/10.1038/s41598-021-82649-8
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author Freitag, Fabio B.
Ahemaiti, Aikeremu
Weman, Hannah M.
Ambroz, Katharina
Lagerström, Malin C.
author_facet Freitag, Fabio B.
Ahemaiti, Aikeremu
Weman, Hannah M.
Ambroz, Katharina
Lagerström, Malin C.
author_sort Freitag, Fabio B.
collection PubMed
description Rodent primary somatosensory cortex (S1) is organized in defined layers, where layer IV serves as the main target for thalamocortical projections. Serotoninergic signaling is important for the organization of thalamocortical projections and consequently proper barrel field development in rodents, and the vesicular monoamine transporter 2 (VMAT2) can be detected locally in layer IV S1 cortical neurons in mice as old as P10, but the identity of the Vmat2-expressing neurons is unknown. We here show that Vmat2 mRNA and also Vmat2-Cre recombinase are still expressed in adult mice in a sub-population of the S1 cortical neurons in the barrel field. The Vmat2-Cre cells showed a homogenous intrinsically bursting firing pattern determined by whole-cell patch-clamp, localized radial densely spinous basal dendritic trees and almost exclusively lack of apical dendrite, indicative of layer IV spiny stellate cells. Single cell mRNA sequencing analysis showed that S1 cortical Vmat2-Cre;tdTomato cells express the layer IV marker Rorb and mainly cluster with layer IV neurons, and RNAscope analysis revealed that adult Vmat2-Cre neurons express Vmat2 and vesicular glutamate transporter 1 (Vglut1) and Vglut2 mRNA to a high extent. In conclusion, our analysis shows that cortical Vmat2 expression is mainly confined to layer IV neurons with morphological, electrophysiological and transcriptional characteristics indicative of spiny stellate cells.
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spelling pubmed-78649352021-02-08 Targeting barrel field spiny stellate cells using a vesicular monoaminergic transporter 2-Cre mouse line Freitag, Fabio B. Ahemaiti, Aikeremu Weman, Hannah M. Ambroz, Katharina Lagerström, Malin C. Sci Rep Article Rodent primary somatosensory cortex (S1) is organized in defined layers, where layer IV serves as the main target for thalamocortical projections. Serotoninergic signaling is important for the organization of thalamocortical projections and consequently proper barrel field development in rodents, and the vesicular monoamine transporter 2 (VMAT2) can be detected locally in layer IV S1 cortical neurons in mice as old as P10, but the identity of the Vmat2-expressing neurons is unknown. We here show that Vmat2 mRNA and also Vmat2-Cre recombinase are still expressed in adult mice in a sub-population of the S1 cortical neurons in the barrel field. The Vmat2-Cre cells showed a homogenous intrinsically bursting firing pattern determined by whole-cell patch-clamp, localized radial densely spinous basal dendritic trees and almost exclusively lack of apical dendrite, indicative of layer IV spiny stellate cells. Single cell mRNA sequencing analysis showed that S1 cortical Vmat2-Cre;tdTomato cells express the layer IV marker Rorb and mainly cluster with layer IV neurons, and RNAscope analysis revealed that adult Vmat2-Cre neurons express Vmat2 and vesicular glutamate transporter 1 (Vglut1) and Vglut2 mRNA to a high extent. In conclusion, our analysis shows that cortical Vmat2 expression is mainly confined to layer IV neurons with morphological, electrophysiological and transcriptional characteristics indicative of spiny stellate cells. Nature Publishing Group UK 2021-02-05 /pmc/articles/PMC7864935/ /pubmed/33547358 http://dx.doi.org/10.1038/s41598-021-82649-8 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Freitag, Fabio B.
Ahemaiti, Aikeremu
Weman, Hannah M.
Ambroz, Katharina
Lagerström, Malin C.
Targeting barrel field spiny stellate cells using a vesicular monoaminergic transporter 2-Cre mouse line
title Targeting barrel field spiny stellate cells using a vesicular monoaminergic transporter 2-Cre mouse line
title_full Targeting barrel field spiny stellate cells using a vesicular monoaminergic transporter 2-Cre mouse line
title_fullStr Targeting barrel field spiny stellate cells using a vesicular monoaminergic transporter 2-Cre mouse line
title_full_unstemmed Targeting barrel field spiny stellate cells using a vesicular monoaminergic transporter 2-Cre mouse line
title_short Targeting barrel field spiny stellate cells using a vesicular monoaminergic transporter 2-Cre mouse line
title_sort targeting barrel field spiny stellate cells using a vesicular monoaminergic transporter 2-cre mouse line
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864935/
https://www.ncbi.nlm.nih.gov/pubmed/33547358
http://dx.doi.org/10.1038/s41598-021-82649-8
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