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Cell Type-Dependent Activation Sequence During Rhythmic Bursting in the PreBötzinger Complex in Respiratory Rhythmic Slices From Mice
Spontaneous respiratory rhythmic burst activity can be preserved in the preBötzinger Complex (preBötC) of rodent medullary transverse slices. It is known, that the activation sequence of inspiratory neurons in the preBötC stochastically varies from cycle to cycle. To test whether the activation timi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129845/ https://www.ncbi.nlm.nih.gov/pubmed/30233397 http://dx.doi.org/10.3389/fphys.2018.01219 |
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author | Oke, Yoshihiko Miwakeichi, Fumikazu Oku, Yoshitaka Hirrlinger, Johannes Hülsmann, Swen |
author_facet | Oke, Yoshihiko Miwakeichi, Fumikazu Oku, Yoshitaka Hirrlinger, Johannes Hülsmann, Swen |
author_sort | Oke, Yoshihiko |
collection | PubMed |
description | Spontaneous respiratory rhythmic burst activity can be preserved in the preBötzinger Complex (preBötC) of rodent medullary transverse slices. It is known, that the activation sequence of inspiratory neurons in the preBötC stochastically varies from cycle to cycle. To test whether the activation timing of an inspiratory neuron depends on its neurotransmitter, we performed calcium imaging of preBötC neurons using double-transgenic mice expressing EGFP in GlyT2(+) neurons and tdTomato in GAD65(+) neurons. Five types of inspiratory neurons were identified using the fluorescence protein expression and the maximum cross-correlation coefficient between neuronal calcium fluctuation and field potential. Regarding the activation sequence, irregular type putative excitatory (GlyT2(-)/GAD65(-)) neurons and irregular type glycinergic (GlyT2(+)/GAD65(-)) neurons tended to be activated early, while regular type putative excitatory neurons, regular type glycinergic neurons tended to be activated later. In conclusion, the different cell types define a general framework for the stochastically changing activation sequence of inspiratory neurons in the preBötC. |
format | Online Article Text |
id | pubmed-6129845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61298452018-09-19 Cell Type-Dependent Activation Sequence During Rhythmic Bursting in the PreBötzinger Complex in Respiratory Rhythmic Slices From Mice Oke, Yoshihiko Miwakeichi, Fumikazu Oku, Yoshitaka Hirrlinger, Johannes Hülsmann, Swen Front Physiol Physiology Spontaneous respiratory rhythmic burst activity can be preserved in the preBötzinger Complex (preBötC) of rodent medullary transverse slices. It is known, that the activation sequence of inspiratory neurons in the preBötC stochastically varies from cycle to cycle. To test whether the activation timing of an inspiratory neuron depends on its neurotransmitter, we performed calcium imaging of preBötC neurons using double-transgenic mice expressing EGFP in GlyT2(+) neurons and tdTomato in GAD65(+) neurons. Five types of inspiratory neurons were identified using the fluorescence protein expression and the maximum cross-correlation coefficient between neuronal calcium fluctuation and field potential. Regarding the activation sequence, irregular type putative excitatory (GlyT2(-)/GAD65(-)) neurons and irregular type glycinergic (GlyT2(+)/GAD65(-)) neurons tended to be activated early, while regular type putative excitatory neurons, regular type glycinergic neurons tended to be activated later. In conclusion, the different cell types define a general framework for the stochastically changing activation sequence of inspiratory neurons in the preBötC. Frontiers Media S.A. 2018-09-03 /pmc/articles/PMC6129845/ /pubmed/30233397 http://dx.doi.org/10.3389/fphys.2018.01219 Text en Copyright © 2018 Oke, Miwakeichi, Oku, Hirrlinger and Hülsmann. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Oke, Yoshihiko Miwakeichi, Fumikazu Oku, Yoshitaka Hirrlinger, Johannes Hülsmann, Swen Cell Type-Dependent Activation Sequence During Rhythmic Bursting in the PreBötzinger Complex in Respiratory Rhythmic Slices From Mice |
title | Cell Type-Dependent Activation Sequence During Rhythmic Bursting in the PreBötzinger Complex in Respiratory Rhythmic Slices From Mice |
title_full | Cell Type-Dependent Activation Sequence During Rhythmic Bursting in the PreBötzinger Complex in Respiratory Rhythmic Slices From Mice |
title_fullStr | Cell Type-Dependent Activation Sequence During Rhythmic Bursting in the PreBötzinger Complex in Respiratory Rhythmic Slices From Mice |
title_full_unstemmed | Cell Type-Dependent Activation Sequence During Rhythmic Bursting in the PreBötzinger Complex in Respiratory Rhythmic Slices From Mice |
title_short | Cell Type-Dependent Activation Sequence During Rhythmic Bursting in the PreBötzinger Complex in Respiratory Rhythmic Slices From Mice |
title_sort | cell type-dependent activation sequence during rhythmic bursting in the prebötzinger complex in respiratory rhythmic slices from mice |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129845/ https://www.ncbi.nlm.nih.gov/pubmed/30233397 http://dx.doi.org/10.3389/fphys.2018.01219 |
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