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The Molecular Fingerprint of Dorsal Root and Trigeminal Ganglion Neurons
The dorsal root ganglia (DRG) and trigeminal ganglia (TG) are clusters of cell bodies of highly specialized sensory neurons which are responsible for relaying information about our environment to the central nervous system. Despite previous efforts to characterize sensory neurons at the molecular le...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623188/ https://www.ncbi.nlm.nih.gov/pubmed/29018326 http://dx.doi.org/10.3389/fnmol.2017.00304 |
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author | Lopes, Douglas M. Denk, Franziska McMahon, Stephen B. |
author_facet | Lopes, Douglas M. Denk, Franziska McMahon, Stephen B. |
author_sort | Lopes, Douglas M. |
collection | PubMed |
description | The dorsal root ganglia (DRG) and trigeminal ganglia (TG) are clusters of cell bodies of highly specialized sensory neurons which are responsible for relaying information about our environment to the central nervous system. Despite previous efforts to characterize sensory neurons at the molecular level, it is still unknown whether those present in DRG and TG have distinct expression profiles and therefore a unique molecular fingerprint. To address this question, we isolated lumbar DRG and TG neurons using fluorescence-activated cell sorting from Advillin-GFP transgenic mice and performed RNA sequencing. Our transcriptome analyses showed that, despite being overwhelmingly similar, a number of genes are differentially expressed in DRG and TG neurons. Importantly, we identified 24 genes which were uniquely expressed in either ganglia, including an arginine vasopressin receptor and several homeobox genes, giving each population a distinct molecular fingerprint. We compared our findings with published studies to reveal that many genes previously reported to be present in neurons are in fact likely to originate from other cell types in the ganglia. Additionally, our neuron-specific results aligned well with a dataset examining whole human TG and DRG. We propose that the data can both improve our understanding of primary afferent biology and help contribute to the development of drug treatments and gene therapies which seek targets with unique or restricted expression patterns. |
format | Online Article Text |
id | pubmed-5623188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56231882017-10-10 The Molecular Fingerprint of Dorsal Root and Trigeminal Ganglion Neurons Lopes, Douglas M. Denk, Franziska McMahon, Stephen B. Front Mol Neurosci Neuroscience The dorsal root ganglia (DRG) and trigeminal ganglia (TG) are clusters of cell bodies of highly specialized sensory neurons which are responsible for relaying information about our environment to the central nervous system. Despite previous efforts to characterize sensory neurons at the molecular level, it is still unknown whether those present in DRG and TG have distinct expression profiles and therefore a unique molecular fingerprint. To address this question, we isolated lumbar DRG and TG neurons using fluorescence-activated cell sorting from Advillin-GFP transgenic mice and performed RNA sequencing. Our transcriptome analyses showed that, despite being overwhelmingly similar, a number of genes are differentially expressed in DRG and TG neurons. Importantly, we identified 24 genes which were uniquely expressed in either ganglia, including an arginine vasopressin receptor and several homeobox genes, giving each population a distinct molecular fingerprint. We compared our findings with published studies to reveal that many genes previously reported to be present in neurons are in fact likely to originate from other cell types in the ganglia. Additionally, our neuron-specific results aligned well with a dataset examining whole human TG and DRG. We propose that the data can both improve our understanding of primary afferent biology and help contribute to the development of drug treatments and gene therapies which seek targets with unique or restricted expression patterns. Frontiers Media S.A. 2017-09-26 /pmc/articles/PMC5623188/ /pubmed/29018326 http://dx.doi.org/10.3389/fnmol.2017.00304 Text en Copyright © 2017 Lopes, Denk and McMahon. 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) or licensor 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 Lopes, Douglas M. Denk, Franziska McMahon, Stephen B. The Molecular Fingerprint of Dorsal Root and Trigeminal Ganglion Neurons |
title | The Molecular Fingerprint of Dorsal Root and Trigeminal Ganglion Neurons |
title_full | The Molecular Fingerprint of Dorsal Root and Trigeminal Ganglion Neurons |
title_fullStr | The Molecular Fingerprint of Dorsal Root and Trigeminal Ganglion Neurons |
title_full_unstemmed | The Molecular Fingerprint of Dorsal Root and Trigeminal Ganglion Neurons |
title_short | The Molecular Fingerprint of Dorsal Root and Trigeminal Ganglion Neurons |
title_sort | molecular fingerprint of dorsal root and trigeminal ganglion neurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623188/ https://www.ncbi.nlm.nih.gov/pubmed/29018326 http://dx.doi.org/10.3389/fnmol.2017.00304 |
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