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Comparative transcriptomics reveals highly conserved regional programs between porcine and human colonic enteric nervous system
The porcine gut is increasingly regarded as a useful translational model. The enteric nervous system in the colon coordinates diverse functions. However, knowledge of the molecular profiling of porcine enteric nerve system and its similarity to that of human is still lacking. We identified the disti...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9872754/ https://www.ncbi.nlm.nih.gov/pubmed/36693960 http://dx.doi.org/10.1038/s42003-023-04478-x |
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author | Li, Tao Morselli, Marco Su, Trent Million, Mulugeta Larauche, Muriel Pellegrini, Matteo Taché, Yvette Yuan, Pu-Qing |
author_facet | Li, Tao Morselli, Marco Su, Trent Million, Mulugeta Larauche, Muriel Pellegrini, Matteo Taché, Yvette Yuan, Pu-Qing |
author_sort | Li, Tao |
collection | PubMed |
description | The porcine gut is increasingly regarded as a useful translational model. The enteric nervous system in the colon coordinates diverse functions. However, knowledge of the molecular profiling of porcine enteric nerve system and its similarity to that of human is still lacking. We identified the distinct transcriptional programs associated with functional characteristics between inner submucosal and myenteric ganglia in porcine proximal and distal colon using bulk RNA and single-cell RNA sequencing. Comparative transcriptomics of myenteric ganglia in corresponding colonic regions of pig and human revealed highly conserved programs in porcine proximal and distal colon, which explained >96% of their transcriptomic responses to vagal nerve stimulation, suggesting that porcine proximal and distal colon could serve as predictors in translational studies. The conserved programs specific for inflammatory modulation were displayed in pigs with vagal nerve stimulation. This study provides a valuable transcriptomic resource for understanding of human colonic functions and neuromodulation using porcine model. |
format | Online Article Text |
id | pubmed-9872754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98727542023-01-25 Comparative transcriptomics reveals highly conserved regional programs between porcine and human colonic enteric nervous system Li, Tao Morselli, Marco Su, Trent Million, Mulugeta Larauche, Muriel Pellegrini, Matteo Taché, Yvette Yuan, Pu-Qing Commun Biol Article The porcine gut is increasingly regarded as a useful translational model. The enteric nervous system in the colon coordinates diverse functions. However, knowledge of the molecular profiling of porcine enteric nerve system and its similarity to that of human is still lacking. We identified the distinct transcriptional programs associated with functional characteristics between inner submucosal and myenteric ganglia in porcine proximal and distal colon using bulk RNA and single-cell RNA sequencing. Comparative transcriptomics of myenteric ganglia in corresponding colonic regions of pig and human revealed highly conserved programs in porcine proximal and distal colon, which explained >96% of their transcriptomic responses to vagal nerve stimulation, suggesting that porcine proximal and distal colon could serve as predictors in translational studies. The conserved programs specific for inflammatory modulation were displayed in pigs with vagal nerve stimulation. This study provides a valuable transcriptomic resource for understanding of human colonic functions and neuromodulation using porcine model. Nature Publishing Group UK 2023-01-24 /pmc/articles/PMC9872754/ /pubmed/36693960 http://dx.doi.org/10.1038/s42003-023-04478-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Li, Tao Morselli, Marco Su, Trent Million, Mulugeta Larauche, Muriel Pellegrini, Matteo Taché, Yvette Yuan, Pu-Qing Comparative transcriptomics reveals highly conserved regional programs between porcine and human colonic enteric nervous system |
title | Comparative transcriptomics reveals highly conserved regional programs between porcine and human colonic enteric nervous system |
title_full | Comparative transcriptomics reveals highly conserved regional programs between porcine and human colonic enteric nervous system |
title_fullStr | Comparative transcriptomics reveals highly conserved regional programs between porcine and human colonic enteric nervous system |
title_full_unstemmed | Comparative transcriptomics reveals highly conserved regional programs between porcine and human colonic enteric nervous system |
title_short | Comparative transcriptomics reveals highly conserved regional programs between porcine and human colonic enteric nervous system |
title_sort | comparative transcriptomics reveals highly conserved regional programs between porcine and human colonic enteric nervous system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9872754/ https://www.ncbi.nlm.nih.gov/pubmed/36693960 http://dx.doi.org/10.1038/s42003-023-04478-x |
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