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SCFAs strongly stimulate PYY production in human enteroendocrine cells
Peptide-YY (PYY) and Glucagon-Like Peptide-1 (GLP-1) play important roles in the regulation of food intake and insulin secretion, and are of translational interest in the field of obesity and diabetes. PYY production is highest in enteroendocrine cells located in the distal intestine, mirroring the...
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/PMC5758799/ https://www.ncbi.nlm.nih.gov/pubmed/29311617 http://dx.doi.org/10.1038/s41598-017-18259-0 |
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author | Larraufie, P. Martin-Gallausiaux, C. Lapaque, N. Dore, J. Gribble, F. M. Reimann, F. Blottiere, H. M. |
author_facet | Larraufie, P. Martin-Gallausiaux, C. Lapaque, N. Dore, J. Gribble, F. M. Reimann, F. Blottiere, H. M. |
author_sort | Larraufie, P. |
collection | PubMed |
description | Peptide-YY (PYY) and Glucagon-Like Peptide-1 (GLP-1) play important roles in the regulation of food intake and insulin secretion, and are of translational interest in the field of obesity and diabetes. PYY production is highest in enteroendocrine cells located in the distal intestine, mirroring the sites where high concentrations of short chain fatty acids (SCFAs) are produced by gut microbiota. We show here that propionate and butyrate strongly increased expression of PYY but not GCG in human cell line and intestinal primary culture models. The effect was predominantly attributable to the histone deacetylase inhibitory activity of SCFA and minor, but significant contributions of FFA2 (GPR43). Consistent with the SCFA-dependent elevation of PYY gene expression, we also observed increased basal and stimulated PYY hormone secretion. Interestingly, the transcriptional stimulation of PYY was specific to human-derived cell models and not reproduced in murine primary cultures. This is likely due to substantial differences in PYY gene structure between mouse and human. In summary, this study revealed a strong regulation of PYY production by SCFA that was evident in humans but not mice, and suggests that high fibre diets elevate plasma concentrations of the anorexigenic hormone PYY, both by targeting gene expression and hormone secretion. |
format | Online Article Text |
id | pubmed-5758799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57587992018-01-10 SCFAs strongly stimulate PYY production in human enteroendocrine cells Larraufie, P. Martin-Gallausiaux, C. Lapaque, N. Dore, J. Gribble, F. M. Reimann, F. Blottiere, H. M. Sci Rep Article Peptide-YY (PYY) and Glucagon-Like Peptide-1 (GLP-1) play important roles in the regulation of food intake and insulin secretion, and are of translational interest in the field of obesity and diabetes. PYY production is highest in enteroendocrine cells located in the distal intestine, mirroring the sites where high concentrations of short chain fatty acids (SCFAs) are produced by gut microbiota. We show here that propionate and butyrate strongly increased expression of PYY but not GCG in human cell line and intestinal primary culture models. The effect was predominantly attributable to the histone deacetylase inhibitory activity of SCFA and minor, but significant contributions of FFA2 (GPR43). Consistent with the SCFA-dependent elevation of PYY gene expression, we also observed increased basal and stimulated PYY hormone secretion. Interestingly, the transcriptional stimulation of PYY was specific to human-derived cell models and not reproduced in murine primary cultures. This is likely due to substantial differences in PYY gene structure between mouse and human. In summary, this study revealed a strong regulation of PYY production by SCFA that was evident in humans but not mice, and suggests that high fibre diets elevate plasma concentrations of the anorexigenic hormone PYY, both by targeting gene expression and hormone secretion. Nature Publishing Group UK 2018-01-08 /pmc/articles/PMC5758799/ /pubmed/29311617 http://dx.doi.org/10.1038/s41598-017-18259-0 Text en © The Author(s) 2017 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 Larraufie, P. Martin-Gallausiaux, C. Lapaque, N. Dore, J. Gribble, F. M. Reimann, F. Blottiere, H. M. SCFAs strongly stimulate PYY production in human enteroendocrine cells |
title | SCFAs strongly stimulate PYY production in human enteroendocrine cells |
title_full | SCFAs strongly stimulate PYY production in human enteroendocrine cells |
title_fullStr | SCFAs strongly stimulate PYY production in human enteroendocrine cells |
title_full_unstemmed | SCFAs strongly stimulate PYY production in human enteroendocrine cells |
title_short | SCFAs strongly stimulate PYY production in human enteroendocrine cells |
title_sort | scfas strongly stimulate pyy production in human enteroendocrine cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758799/ https://www.ncbi.nlm.nih.gov/pubmed/29311617 http://dx.doi.org/10.1038/s41598-017-18259-0 |
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