Cargando…
Gut microbiota regulates maturation of the adult enteric nervous system via enteric serotonin networks
The enteric nervous system (ENS) is crucial for essential gastrointestinal physiologic functions such as motility, fluid secretion, and blood flow. The gut is colonized by trillions of bacteria that regulate host production of several signaling molecules including serotonin (5-HT) and other hormones...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016808/ https://www.ncbi.nlm.nih.gov/pubmed/29866843 http://dx.doi.org/10.1073/pnas.1720017115 |
_version_ | 1783334615632576512 |
---|---|
author | De Vadder, Filipe Grasset, Estelle Mannerås Holm, Louise Karsenty, Gérard Macpherson, Andrew J. Olofsson, Louise E. Bäckhed, Fredrik |
author_facet | De Vadder, Filipe Grasset, Estelle Mannerås Holm, Louise Karsenty, Gérard Macpherson, Andrew J. Olofsson, Louise E. Bäckhed, Fredrik |
author_sort | De Vadder, Filipe |
collection | PubMed |
description | The enteric nervous system (ENS) is crucial for essential gastrointestinal physiologic functions such as motility, fluid secretion, and blood flow. The gut is colonized by trillions of bacteria that regulate host production of several signaling molecules including serotonin (5-HT) and other hormones and neurotransmitters. Approximately 90% of 5-HT originates from the intestine, and activation of the 5-HT(4) receptor in the ENS has been linked to adult neurogenesis and neuroprotection. Here, we tested the hypothesis that the gut microbiota could induce maturation of the adult ENS through release of 5-HT and activation of 5-HT(4) receptors. Colonization of germ-free mice with a microbiota from conventionally raised mice modified the neuroanatomy of the ENS and increased intestinal transit rates, which was associated with neuronal and mucosal 5-HT production and the proliferation of enteric neuronal progenitors in the adult intestine. Pharmacological modulation of the 5-HT(4) receptor, as well as depletion of endogenous 5-HT, identified a mechanistic link between the gut microbiota and maturation of the adult ENS through the release of 5-HT and activation of the 5-HT(4) receptor. Taken together, these findings show that the microbiota modulates the anatomy of the adult ENS in a 5-HT–dependent fashion with concomitant changes in intestinal transit. |
format | Online Article Text |
id | pubmed-6016808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-60168082018-06-26 Gut microbiota regulates maturation of the adult enteric nervous system via enteric serotonin networks De Vadder, Filipe Grasset, Estelle Mannerås Holm, Louise Karsenty, Gérard Macpherson, Andrew J. Olofsson, Louise E. Bäckhed, Fredrik Proc Natl Acad Sci U S A Biological Sciences The enteric nervous system (ENS) is crucial for essential gastrointestinal physiologic functions such as motility, fluid secretion, and blood flow. The gut is colonized by trillions of bacteria that regulate host production of several signaling molecules including serotonin (5-HT) and other hormones and neurotransmitters. Approximately 90% of 5-HT originates from the intestine, and activation of the 5-HT(4) receptor in the ENS has been linked to adult neurogenesis and neuroprotection. Here, we tested the hypothesis that the gut microbiota could induce maturation of the adult ENS through release of 5-HT and activation of 5-HT(4) receptors. Colonization of germ-free mice with a microbiota from conventionally raised mice modified the neuroanatomy of the ENS and increased intestinal transit rates, which was associated with neuronal and mucosal 5-HT production and the proliferation of enteric neuronal progenitors in the adult intestine. Pharmacological modulation of the 5-HT(4) receptor, as well as depletion of endogenous 5-HT, identified a mechanistic link between the gut microbiota and maturation of the adult ENS through the release of 5-HT and activation of the 5-HT(4) receptor. Taken together, these findings show that the microbiota modulates the anatomy of the adult ENS in a 5-HT–dependent fashion with concomitant changes in intestinal transit. National Academy of Sciences 2018-06-19 2018-06-04 /pmc/articles/PMC6016808/ /pubmed/29866843 http://dx.doi.org/10.1073/pnas.1720017115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences De Vadder, Filipe Grasset, Estelle Mannerås Holm, Louise Karsenty, Gérard Macpherson, Andrew J. Olofsson, Louise E. Bäckhed, Fredrik Gut microbiota regulates maturation of the adult enteric nervous system via enteric serotonin networks |
title | Gut microbiota regulates maturation of the adult enteric nervous system via enteric serotonin networks |
title_full | Gut microbiota regulates maturation of the adult enteric nervous system via enteric serotonin networks |
title_fullStr | Gut microbiota regulates maturation of the adult enteric nervous system via enteric serotonin networks |
title_full_unstemmed | Gut microbiota regulates maturation of the adult enteric nervous system via enteric serotonin networks |
title_short | Gut microbiota regulates maturation of the adult enteric nervous system via enteric serotonin networks |
title_sort | gut microbiota regulates maturation of the adult enteric nervous system via enteric serotonin networks |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016808/ https://www.ncbi.nlm.nih.gov/pubmed/29866843 http://dx.doi.org/10.1073/pnas.1720017115 |
work_keys_str_mv | AT devadderfilipe gutmicrobiotaregulatesmaturationoftheadultentericnervoussystemviaentericserotoninnetworks AT grassetestelle gutmicrobiotaregulatesmaturationoftheadultentericnervoussystemviaentericserotoninnetworks AT mannerasholmlouise gutmicrobiotaregulatesmaturationoftheadultentericnervoussystemviaentericserotoninnetworks AT karsentygerard gutmicrobiotaregulatesmaturationoftheadultentericnervoussystemviaentericserotoninnetworks AT macphersonandrewj gutmicrobiotaregulatesmaturationoftheadultentericnervoussystemviaentericserotoninnetworks AT olofssonlouisee gutmicrobiotaregulatesmaturationoftheadultentericnervoussystemviaentericserotoninnetworks AT backhedfredrik gutmicrobiotaregulatesmaturationoftheadultentericnervoussystemviaentericserotoninnetworks |