Gut microbiota regulation of P-glycoprotein in the intestinal epithelium in maintenance of homeostasis
dc.contributor.author | Foley, Sage E | |
dc.contributor.author | Tuohy, Christine | |
dc.contributor.author | Dunford, Merran | |
dc.contributor.author | Grey, Michael J. | |
dc.contributor.author | De Luca, Heidi | |
dc.contributor.author | Cawley, Caitlin | |
dc.contributor.author | Szabady, Rose L. | |
dc.contributor.author | Maldonado-Contreras, Ana | |
dc.contributor.author | Houghton, JeanMarie | |
dc.contributor.author | Ward, Doyle V | |
dc.contributor.author | Mrsny, Randall J. | |
dc.contributor.author | McCormick, Beth A. | |
dc.date | 2022-08-11T08:10:06.000 | |
dc.date.accessioned | 2022-08-23T16:55:14Z | |
dc.date.available | 2022-08-23T16:55:14Z | |
dc.date.issued | 2021-09-07 | |
dc.date.submitted | 2022-04-21 | |
dc.identifier.citation | <p>Foley SE, Tuohy C, Dunford M, Grey MJ, De Luca H, Cawley C, Szabady RL, Maldonado-Contreras A, Houghton JM, Ward DV, Mrsny RJ, McCormick BA. Gut microbiota regulation of P-glycoprotein in the intestinal epithelium in maintenance of homeostasis. Microbiome. 2021 Sep 7;9(1):183. doi: 10.1186/s40168-021-01137-3. PMID: 34493329; PMCID: PMC8425172. <a href="https://doi.org/10.1186/s40168-021-01137-3">Link to article on publisher's site</a></p> | |
dc.identifier.issn | 2049-2618 (Linking) | |
dc.identifier.doi | 10.1186/s40168-021-01137-3 | |
dc.identifier.pmid | 34493329 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/42673 | |
dc.description.abstract | BACKGROUND: P-glycoprotein (P-gp) plays a critical role in protection of the intestinal epithelia by mediating efflux of drugs/xenobiotics from the intestinal mucosa into the gut lumen. Recent studies bring to light that P-gp also confers a critical link in communication between intestinal mucosal barrier function and the innate immune system. Yet, despite knowledge for over 10 years that P-gp plays a central role in gastrointestinal homeostasis, the precise molecular mechanism that controls its functional expression and regulation remains unclear. Here, we assessed how the intestinal microbiome drives P-gp expression and function. RESULTS: We have identified a "functional core" microbiome of the intestinal gut community, specifically genera within the Clostridia and Bacilli classes, that is necessary and sufficient for P-gp induction in the intestinal epithelium in mouse models. Metagenomic analysis of this core microbial community revealed that short-chain fatty acid and secondary bile acid production positively associate with P-gp expression. We have further shown these two classes of microbiota-derived metabolites synergistically upregulate P-gp expression and function in vitro and in vivo. Moreover, in patients suffering from ulcerative colitis (UC), we find diminished P-gp expression coupled to the reduction of epithelial-derived anti-inflammatory endocannabinoids and luminal content (e.g., microbes or their metabolites) with a reduced capability to induce P-gp expression. CONCLUSION: Overall, by means of both in vitro and in vivo studies as well as human subject sample analysis, we identify a mechanistic link between cooperative functional outputs of the complex microbial community and modulation of P-gp, an epithelial component, that functions to suppress overactive inflammation to maintain intestinal homeostasis. Hence, our data support a new cross-talk paradigm in microbiome regulation of mucosal inflammation. Video abstract. | |
dc.language.iso | en_US | |
dc.relation | <p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=34493329&dopt=Abstract">Link to Article in PubMed</a></p> | |
dc.rights | Copyright © The Author(s) 2021. 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Endocannabinoid | |
dc.subject | Inflammation | |
dc.subject | Inflammatory bowel diseases | |
dc.subject | Intestinal epithelium | |
dc.subject | Microbiome | |
dc.subject | Multi-drug resistance transporter | |
dc.subject | P-glycoprotein | |
dc.subject | Secondary bile acids | |
dc.subject | Short-chain fatty acids | |
dc.subject | Ulcerative colitis | |
dc.subject | Amino Acids, Peptides, and Proteins | |
dc.subject | Digestive System Diseases | |
dc.subject | Gastroenterology | |
dc.subject | Microbiology | |
dc.title | Gut microbiota regulation of P-glycoprotein in the intestinal epithelium in maintenance of homeostasis | |
dc.type | Journal Article | |
dc.source.journaltitle | Microbiome | |
dc.source.volume | 9 | |
dc.source.issue | 1 | |
dc.identifier.legacyfulltext | https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=5951&context=oapubs&unstamped=1 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/oapubs/4917 | |
dc.identifier.contextkey | 28760666 | |
refterms.dateFOA | 2022-08-23T16:55:14Z | |
html.description.abstract | <p>BACKGROUND: P-glycoprotein (P-gp) plays a critical role in protection of the intestinal epithelia by mediating efflux of drugs/xenobiotics from the intestinal mucosa into the gut lumen. Recent studies bring to light that P-gp also confers a critical link in communication between intestinal mucosal barrier function and the innate immune system. Yet, despite knowledge for over 10 years that P-gp plays a central role in gastrointestinal homeostasis, the precise molecular mechanism that controls its functional expression and regulation remains unclear. Here, we assessed how the intestinal microbiome drives P-gp expression and function.</p> <p>RESULTS: We have identified a "functional core" microbiome of the intestinal gut community, specifically genera within the Clostridia and Bacilli classes, that is necessary and sufficient for P-gp induction in the intestinal epithelium in mouse models. Metagenomic analysis of this core microbial community revealed that short-chain fatty acid and secondary bile acid production positively associate with P-gp expression. We have further shown these two classes of microbiota-derived metabolites synergistically upregulate P-gp expression and function in vitro and in vivo. Moreover, in patients suffering from ulcerative colitis (UC), we find diminished P-gp expression coupled to the reduction of epithelial-derived anti-inflammatory endocannabinoids and luminal content (e.g., microbes or their metabolites) with a reduced capability to induce P-gp expression.</p> <p>CONCLUSION: Overall, by means of both in vitro and in vivo studies as well as human subject sample analysis, we identify a mechanistic link between cooperative functional outputs of the complex microbial community and modulation of P-gp, an epithelial component, that functions to suppress overactive inflammation to maintain intestinal homeostasis. Hence, our data support a new cross-talk paradigm in microbiome regulation of mucosal inflammation. Video abstract.</p> | |
dc.identifier.submissionpath | oapubs/4917 | |
dc.contributor.department | Division of Gastroenterology, Department of Medicine | |
dc.contributor.department | Graduate School of Nursing | |
dc.contributor.department | Program in Microbiome Dynamics | |
dc.contributor.department | Department of Microbiology and Physiological Systems | |
dc.source.pages | 183 |