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Transcriptional Profiling of Somatostatin Interneurons in the Spinal Dorsal Horn

The spinal dorsal horn (SDH) is comprised of distinct neuronal populations that process different somatosensory modalities. Somatostatin (SST)-expressing interneurons in the SDH have been implicated specifically in mediating mechanical pain. Identifying the transcriptomic profile of SST neurons coul...

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Autores principales: Chamessian, Alexander, Young, Michael, Qadri, Yawar, Berta, Temugin, Ji, Ru-Rong, Van de Ven, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931607/
https://www.ncbi.nlm.nih.gov/pubmed/29717160
http://dx.doi.org/10.1038/s41598-018-25110-7
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author Chamessian, Alexander
Young, Michael
Qadri, Yawar
Berta, Temugin
Ji, Ru-Rong
Van de Ven, Thomas
author_facet Chamessian, Alexander
Young, Michael
Qadri, Yawar
Berta, Temugin
Ji, Ru-Rong
Van de Ven, Thomas
author_sort Chamessian, Alexander
collection PubMed
description The spinal dorsal horn (SDH) is comprised of distinct neuronal populations that process different somatosensory modalities. Somatostatin (SST)-expressing interneurons in the SDH have been implicated specifically in mediating mechanical pain. Identifying the transcriptomic profile of SST neurons could elucidate the unique genetic features of this population and enable selective analgesic targeting. To that end, we combined the Isolation of Nuclei Tagged in Specific Cell Types (INTACT) method and Fluorescence Activated Nuclei Sorting (FANS) to capture tagged SST nuclei in the SDH of adult male mice. Using RNA-sequencing (RNA-seq), we uncovered more than 13,000 genes. Differential gene expression analysis revealed more than 900 genes with at least 2-fold enrichment. In addition to many known dorsal horn genes, we identified and validated several novel transcripts from pharmacologically tractable functional classes: Carbonic Anhydrase 12 (Car12), Phosphodiesterase 11 A (Pde11a), and Protease-Activated Receptor 3 (F2rl2). In situ hybridization of these novel genes showed differential expression patterns in the SDH, demonstrating the presence of transcriptionally distinct subpopulations within the SST population. Overall, our findings provide new insights into the gene repertoire of SST dorsal horn neurons and reveal several novel targets for pharmacological modulation of this pain-mediating population and treatment of pathological pain.
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spelling pubmed-59316072018-08-29 Transcriptional Profiling of Somatostatin Interneurons in the Spinal Dorsal Horn Chamessian, Alexander Young, Michael Qadri, Yawar Berta, Temugin Ji, Ru-Rong Van de Ven, Thomas Sci Rep Article The spinal dorsal horn (SDH) is comprised of distinct neuronal populations that process different somatosensory modalities. Somatostatin (SST)-expressing interneurons in the SDH have been implicated specifically in mediating mechanical pain. Identifying the transcriptomic profile of SST neurons could elucidate the unique genetic features of this population and enable selective analgesic targeting. To that end, we combined the Isolation of Nuclei Tagged in Specific Cell Types (INTACT) method and Fluorescence Activated Nuclei Sorting (FANS) to capture tagged SST nuclei in the SDH of adult male mice. Using RNA-sequencing (RNA-seq), we uncovered more than 13,000 genes. Differential gene expression analysis revealed more than 900 genes with at least 2-fold enrichment. In addition to many known dorsal horn genes, we identified and validated several novel transcripts from pharmacologically tractable functional classes: Carbonic Anhydrase 12 (Car12), Phosphodiesterase 11 A (Pde11a), and Protease-Activated Receptor 3 (F2rl2). In situ hybridization of these novel genes showed differential expression patterns in the SDH, demonstrating the presence of transcriptionally distinct subpopulations within the SST population. Overall, our findings provide new insights into the gene repertoire of SST dorsal horn neurons and reveal several novel targets for pharmacological modulation of this pain-mediating population and treatment of pathological pain. Nature Publishing Group UK 2018-05-01 /pmc/articles/PMC5931607/ /pubmed/29717160 http://dx.doi.org/10.1038/s41598-018-25110-7 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chamessian, Alexander
Young, Michael
Qadri, Yawar
Berta, Temugin
Ji, Ru-Rong
Van de Ven, Thomas
Transcriptional Profiling of Somatostatin Interneurons in the Spinal Dorsal Horn
title Transcriptional Profiling of Somatostatin Interneurons in the Spinal Dorsal Horn
title_full Transcriptional Profiling of Somatostatin Interneurons in the Spinal Dorsal Horn
title_fullStr Transcriptional Profiling of Somatostatin Interneurons in the Spinal Dorsal Horn
title_full_unstemmed Transcriptional Profiling of Somatostatin Interneurons in the Spinal Dorsal Horn
title_short Transcriptional Profiling of Somatostatin Interneurons in the Spinal Dorsal Horn
title_sort transcriptional profiling of somatostatin interneurons in the spinal dorsal horn
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931607/
https://www.ncbi.nlm.nih.gov/pubmed/29717160
http://dx.doi.org/10.1038/s41598-018-25110-7
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