Cargando…
Dbx1 precursor cells are a source of inspiratory XII premotoneurons
All behaviors require coordinated activation of motoneurons from central command and premotor networks. The genetic identities of premotoneurons providing behaviorally relevant excitation to any pool of respiratory motoneurons remain unknown. Recently, we established in vitro that Dbx1-derived pre-B...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764567/ https://www.ncbi.nlm.nih.gov/pubmed/26687006 http://dx.doi.org/10.7554/eLife.12301 |
_version_ | 1782417393302110208 |
---|---|
author | Revill, Ann L Vann, Nikolas C Akins, Victoria T Kottick, Andrew Gray, Paul A Del Negro, Christopher A Funk, Gregory D |
author_facet | Revill, Ann L Vann, Nikolas C Akins, Victoria T Kottick, Andrew Gray, Paul A Del Negro, Christopher A Funk, Gregory D |
author_sort | Revill, Ann L |
collection | PubMed |
description | All behaviors require coordinated activation of motoneurons from central command and premotor networks. The genetic identities of premotoneurons providing behaviorally relevant excitation to any pool of respiratory motoneurons remain unknown. Recently, we established in vitro that Dbx1-derived pre-Bötzinger complex neurons are critical for rhythm generation and that a subpopulation serves a premotor function (Wang et al., 2014). Here, we further show that a subpopulation of Dbx1-derived intermediate reticular (IRt) neurons are rhythmically active during inspiration and project to the hypoglossal (XII) nucleus that contains motoneurons important for maintaining airway patency. Laser ablation of Dbx1 IRt neurons, 57% of which are glutamatergic, decreased ipsilateral inspiratory motor output without affecting frequency. We conclude that a subset of Dbx1 IRt neurons is a source of premotor excitatory drive, contributing to the inspiratory behavior of XII motoneurons, as well as a key component of the airway control network whose dysfunction contributes to sleep apnea. DOI: http://dx.doi.org/10.7554/eLife.12301.001 |
format | Online Article Text |
id | pubmed-4764567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47645672016-02-25 Dbx1 precursor cells are a source of inspiratory XII premotoneurons Revill, Ann L Vann, Nikolas C Akins, Victoria T Kottick, Andrew Gray, Paul A Del Negro, Christopher A Funk, Gregory D eLife Neuroscience All behaviors require coordinated activation of motoneurons from central command and premotor networks. The genetic identities of premotoneurons providing behaviorally relevant excitation to any pool of respiratory motoneurons remain unknown. Recently, we established in vitro that Dbx1-derived pre-Bötzinger complex neurons are critical for rhythm generation and that a subpopulation serves a premotor function (Wang et al., 2014). Here, we further show that a subpopulation of Dbx1-derived intermediate reticular (IRt) neurons are rhythmically active during inspiration and project to the hypoglossal (XII) nucleus that contains motoneurons important for maintaining airway patency. Laser ablation of Dbx1 IRt neurons, 57% of which are glutamatergic, decreased ipsilateral inspiratory motor output without affecting frequency. We conclude that a subset of Dbx1 IRt neurons is a source of premotor excitatory drive, contributing to the inspiratory behavior of XII motoneurons, as well as a key component of the airway control network whose dysfunction contributes to sleep apnea. DOI: http://dx.doi.org/10.7554/eLife.12301.001 eLife Sciences Publications, Ltd 2015-12-19 /pmc/articles/PMC4764567/ /pubmed/26687006 http://dx.doi.org/10.7554/eLife.12301 Text en © 2015, Revill et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Revill, Ann L Vann, Nikolas C Akins, Victoria T Kottick, Andrew Gray, Paul A Del Negro, Christopher A Funk, Gregory D Dbx1 precursor cells are a source of inspiratory XII premotoneurons |
title | Dbx1 precursor cells are a source of inspiratory XII premotoneurons |
title_full | Dbx1 precursor cells are a source of inspiratory XII premotoneurons |
title_fullStr | Dbx1 precursor cells are a source of inspiratory XII premotoneurons |
title_full_unstemmed | Dbx1 precursor cells are a source of inspiratory XII premotoneurons |
title_short | Dbx1 precursor cells are a source of inspiratory XII premotoneurons |
title_sort | dbx1 precursor cells are a source of inspiratory xii premotoneurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764567/ https://www.ncbi.nlm.nih.gov/pubmed/26687006 http://dx.doi.org/10.7554/eLife.12301 |
work_keys_str_mv | AT revillannl dbx1precursorcellsareasourceofinspiratoryxiipremotoneurons AT vannnikolasc dbx1precursorcellsareasourceofinspiratoryxiipremotoneurons AT akinsvictoriat dbx1precursorcellsareasourceofinspiratoryxiipremotoneurons AT kottickandrew dbx1precursorcellsareasourceofinspiratoryxiipremotoneurons AT graypaula dbx1precursorcellsareasourceofinspiratoryxiipremotoneurons AT delnegrochristophera dbx1precursorcellsareasourceofinspiratoryxiipremotoneurons AT funkgregoryd dbx1precursorcellsareasourceofinspiratoryxiipremotoneurons |