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Comprehensive analysis of cellular specializations that initiate parallel auditory processing pathways in mice
The cochlear nuclear complex (CN) is the starting point for all central auditory processing and comprises a suite of neuronal cell types that are highly specialized for neural coding of acoustic signals. To examine how their striking functional specializations are determined at the molecular level,...
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/PMC10245571/ https://www.ncbi.nlm.nih.gov/pubmed/37293040 http://dx.doi.org/10.1101/2023.05.15.539065 |
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author | Jing, Junzhan Hu, Ming Ngodup, Tenzin Ma, Qianqian Lau, Shu-Ning Natalie Ljungberg, Cecilia McGinley, Matthew J. Trussell, Laurence O. Jiang, Xiaolong |
author_facet | Jing, Junzhan Hu, Ming Ngodup, Tenzin Ma, Qianqian Lau, Shu-Ning Natalie Ljungberg, Cecilia McGinley, Matthew J. Trussell, Laurence O. Jiang, Xiaolong |
author_sort | Jing, Junzhan |
collection | PubMed |
description | The cochlear nuclear complex (CN) is the starting point for all central auditory processing and comprises a suite of neuronal cell types that are highly specialized for neural coding of acoustic signals. To examine how their striking functional specializations are determined at the molecular level, we performed single-nucleus RNA sequencing of the mouse CN to molecularly define all constituent cell types and related them to morphologically- and electrophysiologically-defined neurons using Patch-seq. We reveal an expanded set of molecular cell types encompassing all previously described major types and discover new subtypes both in terms of topographic and cell-physiologic properties. Our results define a complete cell-type taxonomy in CN that reconciles anatomical position, morphological, physiological, and molecular criteria. This high-resolution account of cellular heterogeneity and specializations from the molecular to the circuit level illustrates molecular underpinnings of functional specializations and enables genetic dissection of auditory processing and hearing disorders with unprecedented specificity. |
format | Online Article Text |
id | pubmed-10245571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-102455712023-06-08 Comprehensive analysis of cellular specializations that initiate parallel auditory processing pathways in mice Jing, Junzhan Hu, Ming Ngodup, Tenzin Ma, Qianqian Lau, Shu-Ning Natalie Ljungberg, Cecilia McGinley, Matthew J. Trussell, Laurence O. Jiang, Xiaolong bioRxiv Article The cochlear nuclear complex (CN) is the starting point for all central auditory processing and comprises a suite of neuronal cell types that are highly specialized for neural coding of acoustic signals. To examine how their striking functional specializations are determined at the molecular level, we performed single-nucleus RNA sequencing of the mouse CN to molecularly define all constituent cell types and related them to morphologically- and electrophysiologically-defined neurons using Patch-seq. We reveal an expanded set of molecular cell types encompassing all previously described major types and discover new subtypes both in terms of topographic and cell-physiologic properties. Our results define a complete cell-type taxonomy in CN that reconciles anatomical position, morphological, physiological, and molecular criteria. This high-resolution account of cellular heterogeneity and specializations from the molecular to the circuit level illustrates molecular underpinnings of functional specializations and enables genetic dissection of auditory processing and hearing disorders with unprecedented specificity. Cold Spring Harbor Laboratory 2023-10-29 /pmc/articles/PMC10245571/ /pubmed/37293040 http://dx.doi.org/10.1101/2023.05.15.539065 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 Jing, Junzhan Hu, Ming Ngodup, Tenzin Ma, Qianqian Lau, Shu-Ning Natalie Ljungberg, Cecilia McGinley, Matthew J. Trussell, Laurence O. Jiang, Xiaolong Comprehensive analysis of cellular specializations that initiate parallel auditory processing pathways in mice |
title | Comprehensive analysis of cellular specializations that initiate parallel auditory processing pathways in mice |
title_full | Comprehensive analysis of cellular specializations that initiate parallel auditory processing pathways in mice |
title_fullStr | Comprehensive analysis of cellular specializations that initiate parallel auditory processing pathways in mice |
title_full_unstemmed | Comprehensive analysis of cellular specializations that initiate parallel auditory processing pathways in mice |
title_short | Comprehensive analysis of cellular specializations that initiate parallel auditory processing pathways in mice |
title_sort | comprehensive analysis of cellular specializations that initiate parallel auditory processing pathways in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245571/ https://www.ncbi.nlm.nih.gov/pubmed/37293040 http://dx.doi.org/10.1101/2023.05.15.539065 |
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