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Enteric Nervous System Regulation of Intestinal Stem Cell Differentiation and Epithelial Monolayer Function
The Enteric Nervous System (ENS) is a complex network of neurons and glia, which regulates sensorimotor function throughout the gastroinestinal tract (GI). Here we investigated the role of the ENS and intestinal myofibroblasts in the maintenance of a primary intestinal epithelial barrier through reg...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5910425/ https://www.ncbi.nlm.nih.gov/pubmed/29679034 http://dx.doi.org/10.1038/s41598-018-24768-3 |
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author | Puzan, Marissa Hosic, Sanjin Ghio, Caroline Koppes, Abigail |
author_facet | Puzan, Marissa Hosic, Sanjin Ghio, Caroline Koppes, Abigail |
author_sort | Puzan, Marissa |
collection | PubMed |
description | The Enteric Nervous System (ENS) is a complex network of neurons and glia, which regulates sensorimotor function throughout the gastroinestinal tract (GI). Here we investigated the role of the ENS and intestinal myofibroblasts in the maintenance of a primary intestinal epithelial barrier through regulation of monolayer permeability, cytokine production, and differentiation of intestinal stem cells. Utilizing a novel, in vitro, transwell-based coculture system, murine small intestinal stem cells were isolated and cultured with ENS neurons and glia or subepithelial myofibroblasts. Results show that the ENS contributes to regulation of intestinal stem cell fate, promoting differentiation into chemosensory enteroendocrine cells, with 0.9% of cells expressing chromogranin A when cultured with ENS versus 0.6% in cocultures with myofibroblasts and 0.3% in epithelial cultures alone. Additionally, enteric neurons and myofibroblasts differentially release cytokines Macrophage Inflammatory Protein 2 (MIP-2), Transforming Growth Factor beta 1 (TGF-β1), and Interleukin 10 (IL-10) when cultured with intestinal epithelial cells, with a 1.5 fold increase of IL-10 and a 3 fold increase in MIP-2 in ENS cocultures compared to coculture with myofibroblasts. These results indicate the importance of enteric populations in the regulation of intestinal barrier function. |
format | Online Article Text |
id | pubmed-5910425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59104252018-04-30 Enteric Nervous System Regulation of Intestinal Stem Cell Differentiation and Epithelial Monolayer Function Puzan, Marissa Hosic, Sanjin Ghio, Caroline Koppes, Abigail Sci Rep Article The Enteric Nervous System (ENS) is a complex network of neurons and glia, which regulates sensorimotor function throughout the gastroinestinal tract (GI). Here we investigated the role of the ENS and intestinal myofibroblasts in the maintenance of a primary intestinal epithelial barrier through regulation of monolayer permeability, cytokine production, and differentiation of intestinal stem cells. Utilizing a novel, in vitro, transwell-based coculture system, murine small intestinal stem cells were isolated and cultured with ENS neurons and glia or subepithelial myofibroblasts. Results show that the ENS contributes to regulation of intestinal stem cell fate, promoting differentiation into chemosensory enteroendocrine cells, with 0.9% of cells expressing chromogranin A when cultured with ENS versus 0.6% in cocultures with myofibroblasts and 0.3% in epithelial cultures alone. Additionally, enteric neurons and myofibroblasts differentially release cytokines Macrophage Inflammatory Protein 2 (MIP-2), Transforming Growth Factor beta 1 (TGF-β1), and Interleukin 10 (IL-10) when cultured with intestinal epithelial cells, with a 1.5 fold increase of IL-10 and a 3 fold increase in MIP-2 in ENS cocultures compared to coculture with myofibroblasts. These results indicate the importance of enteric populations in the regulation of intestinal barrier function. Nature Publishing Group UK 2018-04-20 /pmc/articles/PMC5910425/ /pubmed/29679034 http://dx.doi.org/10.1038/s41598-018-24768-3 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 Puzan, Marissa Hosic, Sanjin Ghio, Caroline Koppes, Abigail Enteric Nervous System Regulation of Intestinal Stem Cell Differentiation and Epithelial Monolayer Function |
title | Enteric Nervous System Regulation of Intestinal Stem Cell Differentiation and Epithelial Monolayer Function |
title_full | Enteric Nervous System Regulation of Intestinal Stem Cell Differentiation and Epithelial Monolayer Function |
title_fullStr | Enteric Nervous System Regulation of Intestinal Stem Cell Differentiation and Epithelial Monolayer Function |
title_full_unstemmed | Enteric Nervous System Regulation of Intestinal Stem Cell Differentiation and Epithelial Monolayer Function |
title_short | Enteric Nervous System Regulation of Intestinal Stem Cell Differentiation and Epithelial Monolayer Function |
title_sort | enteric nervous system regulation of intestinal stem cell differentiation and epithelial monolayer function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5910425/ https://www.ncbi.nlm.nih.gov/pubmed/29679034 http://dx.doi.org/10.1038/s41598-018-24768-3 |
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