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Wt1 Positive dB4 Neurons in the Hindbrain Are Crucial for Respiration
Central pattern generator (CPG) networks coordinate the generation of rhythmic activity such as locomotion and respiration. Their development is driven by various transcription factors, one of which is the Wilms tumor protein (Wt1). It is present in dI6 neurons of the mouse spinal cord, and involved...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734174/ https://www.ncbi.nlm.nih.gov/pubmed/33328840 http://dx.doi.org/10.3389/fnins.2020.529487 |
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author | Schnerwitzki, Danny Hayn, Christian Perner, Birgit Englert, Christoph |
author_facet | Schnerwitzki, Danny Hayn, Christian Perner, Birgit Englert, Christoph |
author_sort | Schnerwitzki, Danny |
collection | PubMed |
description | Central pattern generator (CPG) networks coordinate the generation of rhythmic activity such as locomotion and respiration. Their development is driven by various transcription factors, one of which is the Wilms tumor protein (Wt1). It is present in dI6 neurons of the mouse spinal cord, and involved in the coordination of locomotion. Here we report about the presence of Wt1 in neurons of the caudoventral medulla oblongata and their impact on respiration. By employing immunohistofluorescence staining, we were able to characterize these Wt1 positive (+) cells as dB4 neurons. The temporal occurrence of Wt1 suggests a role for this transcription factor in the differentiation of dB4 neurons during embryonic and postnatal development. Conditional knockout of Wt1 in these cells caused an altered population size of V0 neurons already in the developing hindbrain, leading to a decline in the respiration rate in the adults. Thereby, we confirmed and extended the previously proposed similarity between dB4 neurons in the hindbrain and dI6 neurons of the spinal cord, in terms of development and function. Ablation of Wt1+ dB4 neurons resulted in the death of neonates due to the inability to initiate respiration, suggesting a vital role for Wt1+ dB4 neurons in breathing. These results expand the role of Wt1 in the CNS and show that, in addition to its function in differentiation of dI6 neurons, it also contributes to the development of dB4 neurons in the hindbrain that are critically involved in the regulation of respiration. |
format | Online Article Text |
id | pubmed-7734174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77341742020-12-15 Wt1 Positive dB4 Neurons in the Hindbrain Are Crucial for Respiration Schnerwitzki, Danny Hayn, Christian Perner, Birgit Englert, Christoph Front Neurosci Neuroscience Central pattern generator (CPG) networks coordinate the generation of rhythmic activity such as locomotion and respiration. Their development is driven by various transcription factors, one of which is the Wilms tumor protein (Wt1). It is present in dI6 neurons of the mouse spinal cord, and involved in the coordination of locomotion. Here we report about the presence of Wt1 in neurons of the caudoventral medulla oblongata and their impact on respiration. By employing immunohistofluorescence staining, we were able to characterize these Wt1 positive (+) cells as dB4 neurons. The temporal occurrence of Wt1 suggests a role for this transcription factor in the differentiation of dB4 neurons during embryonic and postnatal development. Conditional knockout of Wt1 in these cells caused an altered population size of V0 neurons already in the developing hindbrain, leading to a decline in the respiration rate in the adults. Thereby, we confirmed and extended the previously proposed similarity between dB4 neurons in the hindbrain and dI6 neurons of the spinal cord, in terms of development and function. Ablation of Wt1+ dB4 neurons resulted in the death of neonates due to the inability to initiate respiration, suggesting a vital role for Wt1+ dB4 neurons in breathing. These results expand the role of Wt1 in the CNS and show that, in addition to its function in differentiation of dI6 neurons, it also contributes to the development of dB4 neurons in the hindbrain that are critically involved in the regulation of respiration. Frontiers Media S.A. 2020-11-30 /pmc/articles/PMC7734174/ /pubmed/33328840 http://dx.doi.org/10.3389/fnins.2020.529487 Text en Copyright © 2020 Schnerwitzki, Hayn, Perner and Englert. 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 | Neuroscience Schnerwitzki, Danny Hayn, Christian Perner, Birgit Englert, Christoph Wt1 Positive dB4 Neurons in the Hindbrain Are Crucial for Respiration |
title | Wt1 Positive dB4 Neurons in the Hindbrain Are Crucial for Respiration |
title_full | Wt1 Positive dB4 Neurons in the Hindbrain Are Crucial for Respiration |
title_fullStr | Wt1 Positive dB4 Neurons in the Hindbrain Are Crucial for Respiration |
title_full_unstemmed | Wt1 Positive dB4 Neurons in the Hindbrain Are Crucial for Respiration |
title_short | Wt1 Positive dB4 Neurons in the Hindbrain Are Crucial for Respiration |
title_sort | wt1 positive db4 neurons in the hindbrain are crucial for respiration |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734174/ https://www.ncbi.nlm.nih.gov/pubmed/33328840 http://dx.doi.org/10.3389/fnins.2020.529487 |
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