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Microbial stimulation of oxytocin release from the intestinal epithelium via secretin signaling
Intestinal microbes impact the health of the intestine and organs distal to the gut. Limosilactobacillus reuteri is a human intestinal microbe that promotes normal gut transit(1), the anti-inflammatory immune system(2–4), wound healing(5–7), normal social behavior in mice(8–10), and prevents bone re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028957/ https://www.ncbi.nlm.nih.gov/pubmed/36945649 http://dx.doi.org/10.1101/2023.03.09.531917 |
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author | Danhof, Heather A. Lee, Jihwan Thapa, Aanchal Britton, Robert A. Di Rienzi, Sara C. |
author_facet | Danhof, Heather A. Lee, Jihwan Thapa, Aanchal Britton, Robert A. Di Rienzi, Sara C. |
author_sort | Danhof, Heather A. |
collection | PubMed |
description | Intestinal microbes impact the health of the intestine and organs distal to the gut. Limosilactobacillus reuteri is a human intestinal microbe that promotes normal gut transit(1), the anti-inflammatory immune system(2–4), wound healing(5–7), normal social behavior in mice(8–10), and prevents bone reabsorption(11–17). Each of these functions is impacted by oxytocin(18–22), and oxytocin signaling is required for L. reuteri-mediated wound healing(5) and social behavior(9); however, the initiating events in the gut that lead to oxytocin stimulation and related beneficial functions remain unknown. Here we found evolutionarily conserved oxytocin production in the intestinal epithelium through analysis of single-cell RNA-Seq datasets and imaging of human and mouse intestinal tissues. Moreover, human intestinal organoids produce oxytocin, demonstrating that the intestinal epithelium is sufficient to produce oxytocin. We subsequently found that L. reuteri facilitates oxytocin secretion directly from human intestinal tissue and human intestinal organoids. Finally, we demonstrate that stimulation of oxytocin secretion by L. reuteri is dependent on the gut hormone secretin, which is produced in enteroendocrine cells(23), while oxytocin itself is produced in enterocytes. Altogether, this work demonstrates that oxytocin is produced and secreted from enterocytes in the intestinal epithelium in response to secretin stimulated by L. reuteri. This work thereby identifies oxytocin as an intestinal hormone and provides mechanistic insight into avenues by which gut microbes promote host health. |
format | Online Article Text |
id | pubmed-10028957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-100289572023-03-22 Microbial stimulation of oxytocin release from the intestinal epithelium via secretin signaling Danhof, Heather A. Lee, Jihwan Thapa, Aanchal Britton, Robert A. Di Rienzi, Sara C. bioRxiv Article Intestinal microbes impact the health of the intestine and organs distal to the gut. Limosilactobacillus reuteri is a human intestinal microbe that promotes normal gut transit(1), the anti-inflammatory immune system(2–4), wound healing(5–7), normal social behavior in mice(8–10), and prevents bone reabsorption(11–17). Each of these functions is impacted by oxytocin(18–22), and oxytocin signaling is required for L. reuteri-mediated wound healing(5) and social behavior(9); however, the initiating events in the gut that lead to oxytocin stimulation and related beneficial functions remain unknown. Here we found evolutionarily conserved oxytocin production in the intestinal epithelium through analysis of single-cell RNA-Seq datasets and imaging of human and mouse intestinal tissues. Moreover, human intestinal organoids produce oxytocin, demonstrating that the intestinal epithelium is sufficient to produce oxytocin. We subsequently found that L. reuteri facilitates oxytocin secretion directly from human intestinal tissue and human intestinal organoids. Finally, we demonstrate that stimulation of oxytocin secretion by L. reuteri is dependent on the gut hormone secretin, which is produced in enteroendocrine cells(23), while oxytocin itself is produced in enterocytes. Altogether, this work demonstrates that oxytocin is produced and secreted from enterocytes in the intestinal epithelium in response to secretin stimulated by L. reuteri. This work thereby identifies oxytocin as an intestinal hormone and provides mechanistic insight into avenues by which gut microbes promote host health. Cold Spring Harbor Laboratory 2023-03-09 /pmc/articles/PMC10028957/ /pubmed/36945649 http://dx.doi.org/10.1101/2023.03.09.531917 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Danhof, Heather A. Lee, Jihwan Thapa, Aanchal Britton, Robert A. Di Rienzi, Sara C. Microbial stimulation of oxytocin release from the intestinal epithelium via secretin signaling |
title | Microbial stimulation of oxytocin release from the intestinal epithelium via secretin signaling |
title_full | Microbial stimulation of oxytocin release from the intestinal epithelium via secretin signaling |
title_fullStr | Microbial stimulation of oxytocin release from the intestinal epithelium via secretin signaling |
title_full_unstemmed | Microbial stimulation of oxytocin release from the intestinal epithelium via secretin signaling |
title_short | Microbial stimulation of oxytocin release from the intestinal epithelium via secretin signaling |
title_sort | microbial stimulation of oxytocin release from the intestinal epithelium via secretin signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028957/ https://www.ncbi.nlm.nih.gov/pubmed/36945649 http://dx.doi.org/10.1101/2023.03.09.531917 |
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