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Spatio-molecular domains identified in the mouse subthalamic nucleus and neighboring glutamatergic and GABAergic brain structures

The subthalamic nucleus (STN) is crucial for normal motor, limbic and associative function. STN dysregulation is correlated with several brain disorders, including Parkinsonʼs disease and obsessive compulsive disorder (OCD), for which high-frequency stimulation of the STN is increasing as therapy. H...

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Autores principales: Wallén-Mackenzie, Åsa, Dumas, Sylvie, Papathanou, Maria, Martis Thiele, Mihaela M., Vlcek, Bianca, König, Niclas, Björklund, Åsa K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334224/
https://www.ncbi.nlm.nih.gov/pubmed/32620779
http://dx.doi.org/10.1038/s42003-020-1028-8
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author Wallén-Mackenzie, Åsa
Dumas, Sylvie
Papathanou, Maria
Martis Thiele, Mihaela M.
Vlcek, Bianca
König, Niclas
Björklund, Åsa K.
author_facet Wallén-Mackenzie, Åsa
Dumas, Sylvie
Papathanou, Maria
Martis Thiele, Mihaela M.
Vlcek, Bianca
König, Niclas
Björklund, Åsa K.
author_sort Wallén-Mackenzie, Åsa
collection PubMed
description The subthalamic nucleus (STN) is crucial for normal motor, limbic and associative function. STN dysregulation is correlated with several brain disorders, including Parkinsonʼs disease and obsessive compulsive disorder (OCD), for which high-frequency stimulation of the STN is increasing as therapy. However, clinical progress is hampered by poor knowledge of the anatomical–functional organization of the STN. Today, experimental mouse genetics provides outstanding capacity for functional decoding, provided selective promoters are available. Here, we implemented single-nuclei RNA sequencing (snRNASeq) of the mouse STN followed through with histological analysis of 16 candidate genes of interest. Our results demonstrate that the mouse STN is composed of at least four spatio-molecularly defined domains, each distinguished by defined sets of promoter activities. Further, molecular profiles dissociate the STN from the adjoining para-STN (PSTN) and neighboring structures of the hypothalamus, mammillary nuclei and zona incerta. Enhanced knowledge of STN´s internal organization should prove useful towards genetics-based functional decoding of this clinically relevant brain structure.
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spelling pubmed-73342242020-07-09 Spatio-molecular domains identified in the mouse subthalamic nucleus and neighboring glutamatergic and GABAergic brain structures Wallén-Mackenzie, Åsa Dumas, Sylvie Papathanou, Maria Martis Thiele, Mihaela M. Vlcek, Bianca König, Niclas Björklund, Åsa K. Commun Biol Article The subthalamic nucleus (STN) is crucial for normal motor, limbic and associative function. STN dysregulation is correlated with several brain disorders, including Parkinsonʼs disease and obsessive compulsive disorder (OCD), for which high-frequency stimulation of the STN is increasing as therapy. However, clinical progress is hampered by poor knowledge of the anatomical–functional organization of the STN. Today, experimental mouse genetics provides outstanding capacity for functional decoding, provided selective promoters are available. Here, we implemented single-nuclei RNA sequencing (snRNASeq) of the mouse STN followed through with histological analysis of 16 candidate genes of interest. Our results demonstrate that the mouse STN is composed of at least four spatio-molecularly defined domains, each distinguished by defined sets of promoter activities. Further, molecular profiles dissociate the STN from the adjoining para-STN (PSTN) and neighboring structures of the hypothalamus, mammillary nuclei and zona incerta. Enhanced knowledge of STN´s internal organization should prove useful towards genetics-based functional decoding of this clinically relevant brain structure. Nature Publishing Group UK 2020-07-03 /pmc/articles/PMC7334224/ /pubmed/32620779 http://dx.doi.org/10.1038/s42003-020-1028-8 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
Wallén-Mackenzie, Åsa
Dumas, Sylvie
Papathanou, Maria
Martis Thiele, Mihaela M.
Vlcek, Bianca
König, Niclas
Björklund, Åsa K.
Spatio-molecular domains identified in the mouse subthalamic nucleus and neighboring glutamatergic and GABAergic brain structures
title Spatio-molecular domains identified in the mouse subthalamic nucleus and neighboring glutamatergic and GABAergic brain structures
title_full Spatio-molecular domains identified in the mouse subthalamic nucleus and neighboring glutamatergic and GABAergic brain structures
title_fullStr Spatio-molecular domains identified in the mouse subthalamic nucleus and neighboring glutamatergic and GABAergic brain structures
title_full_unstemmed Spatio-molecular domains identified in the mouse subthalamic nucleus and neighboring glutamatergic and GABAergic brain structures
title_short Spatio-molecular domains identified in the mouse subthalamic nucleus and neighboring glutamatergic and GABAergic brain structures
title_sort spatio-molecular domains identified in the mouse subthalamic nucleus and neighboring glutamatergic and gabaergic brain structures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334224/
https://www.ncbi.nlm.nih.gov/pubmed/32620779
http://dx.doi.org/10.1038/s42003-020-1028-8
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