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Transcriptomes of electrophysiologically recorded Dbx1-derived respiratory neurons of the preBötzinger complex in neonatal mice

Breathing depends on interneurons in the preBötzinger complex (preBötC) derived from Dbx1-expressing precursors. Here we investigate whether rhythm- and pattern-generating functions reside in discrete classes of Dbx1 preBötC neurons. In a slice model of breathing with ~ 5 s cycle period, putatively...

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Autores principales: Kallurkar, Prajkta S., Picardo, Maria Cristina D., Sugimura, Yae K., Saha, Margaret S., Conradi Smith, Gregory D., Del Negro, Christopher A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861066/
https://www.ncbi.nlm.nih.gov/pubmed/35190626
http://dx.doi.org/10.1038/s41598-022-06834-z
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author Kallurkar, Prajkta S.
Picardo, Maria Cristina D.
Sugimura, Yae K.
Saha, Margaret S.
Conradi Smith, Gregory D.
Del Negro, Christopher A.
author_facet Kallurkar, Prajkta S.
Picardo, Maria Cristina D.
Sugimura, Yae K.
Saha, Margaret S.
Conradi Smith, Gregory D.
Del Negro, Christopher A.
author_sort Kallurkar, Prajkta S.
collection PubMed
description Breathing depends on interneurons in the preBötzinger complex (preBötC) derived from Dbx1-expressing precursors. Here we investigate whether rhythm- and pattern-generating functions reside in discrete classes of Dbx1 preBötC neurons. In a slice model of breathing with ~ 5 s cycle period, putatively rhythmogenic Type-1 Dbx1 preBötC neurons activate 100–300 ms prior to Type-2 neurons, putatively specialized for output pattern, and 300–500 ms prior to the inspiratory motor output. We sequenced Type-1 and Type-2 transcriptomes and identified differential expression of 123 genes including ionotropic receptors (Gria3, Gabra1) that may explain their preinspiratory activation profiles and Ca(2+) signaling (Cracr2a, Sgk1) involved in inspiratory and sigh bursts. Surprisingly, neuropeptide receptors that influence breathing (e.g., µ-opioid and bombesin-like peptide receptors) were only sparsely expressed, which suggests that cognate peptides and opioid drugs exert their profound effects on a small fraction of the preBötC core. These data in the public domain help explain the neural origins of breathing.
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spelling pubmed-88610662022-02-22 Transcriptomes of electrophysiologically recorded Dbx1-derived respiratory neurons of the preBötzinger complex in neonatal mice Kallurkar, Prajkta S. Picardo, Maria Cristina D. Sugimura, Yae K. Saha, Margaret S. Conradi Smith, Gregory D. Del Negro, Christopher A. Sci Rep Article Breathing depends on interneurons in the preBötzinger complex (preBötC) derived from Dbx1-expressing precursors. Here we investigate whether rhythm- and pattern-generating functions reside in discrete classes of Dbx1 preBötC neurons. In a slice model of breathing with ~ 5 s cycle period, putatively rhythmogenic Type-1 Dbx1 preBötC neurons activate 100–300 ms prior to Type-2 neurons, putatively specialized for output pattern, and 300–500 ms prior to the inspiratory motor output. We sequenced Type-1 and Type-2 transcriptomes and identified differential expression of 123 genes including ionotropic receptors (Gria3, Gabra1) that may explain their preinspiratory activation profiles and Ca(2+) signaling (Cracr2a, Sgk1) involved in inspiratory and sigh bursts. Surprisingly, neuropeptide receptors that influence breathing (e.g., µ-opioid and bombesin-like peptide receptors) were only sparsely expressed, which suggests that cognate peptides and opioid drugs exert their profound effects on a small fraction of the preBötC core. These data in the public domain help explain the neural origins of breathing. Nature Publishing Group UK 2022-02-21 /pmc/articles/PMC8861066/ /pubmed/35190626 http://dx.doi.org/10.1038/s41598-022-06834-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kallurkar, Prajkta S.
Picardo, Maria Cristina D.
Sugimura, Yae K.
Saha, Margaret S.
Conradi Smith, Gregory D.
Del Negro, Christopher A.
Transcriptomes of electrophysiologically recorded Dbx1-derived respiratory neurons of the preBötzinger complex in neonatal mice
title Transcriptomes of electrophysiologically recorded Dbx1-derived respiratory neurons of the preBötzinger complex in neonatal mice
title_full Transcriptomes of electrophysiologically recorded Dbx1-derived respiratory neurons of the preBötzinger complex in neonatal mice
title_fullStr Transcriptomes of electrophysiologically recorded Dbx1-derived respiratory neurons of the preBötzinger complex in neonatal mice
title_full_unstemmed Transcriptomes of electrophysiologically recorded Dbx1-derived respiratory neurons of the preBötzinger complex in neonatal mice
title_short Transcriptomes of electrophysiologically recorded Dbx1-derived respiratory neurons of the preBötzinger complex in neonatal mice
title_sort transcriptomes of electrophysiologically recorded dbx1-derived respiratory neurons of the prebötzinger complex in neonatal mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861066/
https://www.ncbi.nlm.nih.gov/pubmed/35190626
http://dx.doi.org/10.1038/s41598-022-06834-z
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