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Neuron-specific spinal cord translatomes reveal a neuropeptide code for mouse dorsal horn excitatory neurons
The spinal dorsal horn harbors a sophisticated and heterogeneous network of excitatory and inhibitory neurons that process peripheral signals encoding different sensory modalities. Although it has long been recognized that this network is crucial both for the separation and the integration of sensor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933427/ https://www.ncbi.nlm.nih.gov/pubmed/33664406 http://dx.doi.org/10.1038/s41598-021-84667-y |
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author | Das Gupta, Rebecca Rani Scheurer, Louis Pelczar, Pawel Wildner, Hendrik Zeilhofer, Hanns Ulrich |
author_facet | Das Gupta, Rebecca Rani Scheurer, Louis Pelczar, Pawel Wildner, Hendrik Zeilhofer, Hanns Ulrich |
author_sort | Das Gupta, Rebecca Rani |
collection | PubMed |
description | The spinal dorsal horn harbors a sophisticated and heterogeneous network of excitatory and inhibitory neurons that process peripheral signals encoding different sensory modalities. Although it has long been recognized that this network is crucial both for the separation and the integration of sensory signals of different modalities, a systematic unbiased approach to the use of specific neuromodulatory systems is still missing. Here, we have used the translating ribosome affinity purification (TRAP) technique to map the translatomes of excitatory glutamatergic (vGluT2(+)) and inhibitory GABA and/or glycinergic (vGAT(+) or Gad67(+)) neurons of the mouse spinal cord. Our analyses demonstrate that inhibitory and excitatory neurons are not only set apart, as expected, by the expression of genes related to the production, release or re-uptake of their principal neurotransmitters and by genes encoding for transcription factors, but also by a differential engagement of neuromodulator, especially neuropeptide, signaling pathways. Subsequent multiplex in situ hybridization revealed eleven neuropeptide genes that are strongly enriched in excitatory dorsal horn neurons and display largely non-overlapping expression patterns closely adhering to the laminar and presumably also functional organization of the spinal cord grey matter. |
format | Online Article Text |
id | pubmed-7933427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79334272021-03-08 Neuron-specific spinal cord translatomes reveal a neuropeptide code for mouse dorsal horn excitatory neurons Das Gupta, Rebecca Rani Scheurer, Louis Pelczar, Pawel Wildner, Hendrik Zeilhofer, Hanns Ulrich Sci Rep Article The spinal dorsal horn harbors a sophisticated and heterogeneous network of excitatory and inhibitory neurons that process peripheral signals encoding different sensory modalities. Although it has long been recognized that this network is crucial both for the separation and the integration of sensory signals of different modalities, a systematic unbiased approach to the use of specific neuromodulatory systems is still missing. Here, we have used the translating ribosome affinity purification (TRAP) technique to map the translatomes of excitatory glutamatergic (vGluT2(+)) and inhibitory GABA and/or glycinergic (vGAT(+) or Gad67(+)) neurons of the mouse spinal cord. Our analyses demonstrate that inhibitory and excitatory neurons are not only set apart, as expected, by the expression of genes related to the production, release or re-uptake of their principal neurotransmitters and by genes encoding for transcription factors, but also by a differential engagement of neuromodulator, especially neuropeptide, signaling pathways. Subsequent multiplex in situ hybridization revealed eleven neuropeptide genes that are strongly enriched in excitatory dorsal horn neurons and display largely non-overlapping expression patterns closely adhering to the laminar and presumably also functional organization of the spinal cord grey matter. Nature Publishing Group UK 2021-03-04 /pmc/articles/PMC7933427/ /pubmed/33664406 http://dx.doi.org/10.1038/s41598-021-84667-y Text en © The Author(s) 2021 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/. |
spellingShingle | Article Das Gupta, Rebecca Rani Scheurer, Louis Pelczar, Pawel Wildner, Hendrik Zeilhofer, Hanns Ulrich Neuron-specific spinal cord translatomes reveal a neuropeptide code for mouse dorsal horn excitatory neurons |
title | Neuron-specific spinal cord translatomes reveal a neuropeptide code for mouse dorsal horn excitatory neurons |
title_full | Neuron-specific spinal cord translatomes reveal a neuropeptide code for mouse dorsal horn excitatory neurons |
title_fullStr | Neuron-specific spinal cord translatomes reveal a neuropeptide code for mouse dorsal horn excitatory neurons |
title_full_unstemmed | Neuron-specific spinal cord translatomes reveal a neuropeptide code for mouse dorsal horn excitatory neurons |
title_short | Neuron-specific spinal cord translatomes reveal a neuropeptide code for mouse dorsal horn excitatory neurons |
title_sort | neuron-specific spinal cord translatomes reveal a neuropeptide code for mouse dorsal horn excitatory neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933427/ https://www.ncbi.nlm.nih.gov/pubmed/33664406 http://dx.doi.org/10.1038/s41598-021-84667-y |
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