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Transepithelial Effect of Probiotics in a Novel Model of Gut Lumen to Nerve Signaling

Recent studies have shown that the gut microbiome changes brain function, behavior, and psychiatric and neurological disorders. The Gut–Brain Axis (GBA) provides a neuronal pathway to explain this. But exactly how do commensal bacteria signal through the epithelial layer of the large intestine to ac...

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Autores principales: Piletz, John E., Cooper, Jason, Chidester, Kevin, Erson, Kyle, Melton, Sydney, Osemeka, Anthony, Patterson, Megan, Strickland, Kyndall, Wan, Jing Xuan, Williams, Kaitlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697698/
https://www.ncbi.nlm.nih.gov/pubmed/36432542
http://dx.doi.org/10.3390/nu14224856
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author Piletz, John E.
Cooper, Jason
Chidester, Kevin
Erson, Kyle
Melton, Sydney
Osemeka, Anthony
Patterson, Megan
Strickland, Kyndall
Wan, Jing Xuan
Williams, Kaitlin
author_facet Piletz, John E.
Cooper, Jason
Chidester, Kevin
Erson, Kyle
Melton, Sydney
Osemeka, Anthony
Patterson, Megan
Strickland, Kyndall
Wan, Jing Xuan
Williams, Kaitlin
author_sort Piletz, John E.
collection PubMed
description Recent studies have shown that the gut microbiome changes brain function, behavior, and psychiatric and neurological disorders. The Gut–Brain Axis (GBA) provides a neuronal pathway to explain this. But exactly how do commensal bacteria signal through the epithelial layer of the large intestine to activate GBA nerve afferents? An in vitro model is described. We differentiated two human cell lines: Caco2Bbe1 into mature epithelium on 0.4-micron filters and then SH-SY5Y into mature neurons in 24-well plates. These were co-cultured by placing the epithelium-laden filters 1 mm above the neurons. Twenty-four hours later they were tri-cultured by apical addition of 10(7) Lactobacillus rhamnosus or Lactobacillus fermentum which settled on the epithelium. Alone, the Caco2bbe1 cells stimulated neurite outgrowth in underlying SH-SY5Y. Beyond this, the lactobacilli were well tolerated and stimulated further neurite outgrowth by 24 h post-treatment, though not passing through the filters. The results provide face validity for a first-of-kind model of transepithelial intestinal lumen-to nerve signaling. The model displays the tight junctional barrier characteristics found in the large intestine while at the same time translating stimulatory signals from the bacteria through epithelial cells to attracted neurons. The model is easy to set-up with components widely available.
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spelling pubmed-96976982022-11-26 Transepithelial Effect of Probiotics in a Novel Model of Gut Lumen to Nerve Signaling Piletz, John E. Cooper, Jason Chidester, Kevin Erson, Kyle Melton, Sydney Osemeka, Anthony Patterson, Megan Strickland, Kyndall Wan, Jing Xuan Williams, Kaitlin Nutrients Article Recent studies have shown that the gut microbiome changes brain function, behavior, and psychiatric and neurological disorders. The Gut–Brain Axis (GBA) provides a neuronal pathway to explain this. But exactly how do commensal bacteria signal through the epithelial layer of the large intestine to activate GBA nerve afferents? An in vitro model is described. We differentiated two human cell lines: Caco2Bbe1 into mature epithelium on 0.4-micron filters and then SH-SY5Y into mature neurons in 24-well plates. These were co-cultured by placing the epithelium-laden filters 1 mm above the neurons. Twenty-four hours later they were tri-cultured by apical addition of 10(7) Lactobacillus rhamnosus or Lactobacillus fermentum which settled on the epithelium. Alone, the Caco2bbe1 cells stimulated neurite outgrowth in underlying SH-SY5Y. Beyond this, the lactobacilli were well tolerated and stimulated further neurite outgrowth by 24 h post-treatment, though not passing through the filters. The results provide face validity for a first-of-kind model of transepithelial intestinal lumen-to nerve signaling. The model displays the tight junctional barrier characteristics found in the large intestine while at the same time translating stimulatory signals from the bacteria through epithelial cells to attracted neurons. The model is easy to set-up with components widely available. MDPI 2022-11-17 /pmc/articles/PMC9697698/ /pubmed/36432542 http://dx.doi.org/10.3390/nu14224856 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Piletz, John E.
Cooper, Jason
Chidester, Kevin
Erson, Kyle
Melton, Sydney
Osemeka, Anthony
Patterson, Megan
Strickland, Kyndall
Wan, Jing Xuan
Williams, Kaitlin
Transepithelial Effect of Probiotics in a Novel Model of Gut Lumen to Nerve Signaling
title Transepithelial Effect of Probiotics in a Novel Model of Gut Lumen to Nerve Signaling
title_full Transepithelial Effect of Probiotics in a Novel Model of Gut Lumen to Nerve Signaling
title_fullStr Transepithelial Effect of Probiotics in a Novel Model of Gut Lumen to Nerve Signaling
title_full_unstemmed Transepithelial Effect of Probiotics in a Novel Model of Gut Lumen to Nerve Signaling
title_short Transepithelial Effect of Probiotics in a Novel Model of Gut Lumen to Nerve Signaling
title_sort transepithelial effect of probiotics in a novel model of gut lumen to nerve signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697698/
https://www.ncbi.nlm.nih.gov/pubmed/36432542
http://dx.doi.org/10.3390/nu14224856
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