Bacteroides thetaiotaomicron relieves colon inflammation by activating aryl hydrocarbon receptor and modulating CD4+T cell homeostasis
•B. thetaiotaomicron treatment ameliorates clinical signs of disease in DSS-induced colitis.•B. thetaiotaomicron enhanced the differentiation of Treg/Th2 cells and reduced the development of Th1/Th17 cells.•B. thetaiotaomicron significantly increase FoxP3 expression and demethylates several CpG site...
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description | •B. thetaiotaomicron treatment ameliorates clinical signs of disease in DSS-induced colitis.•B. thetaiotaomicron enhanced the differentiation of Treg/Th2 cells and reduced the development of Th1/Th17 cells.•B. thetaiotaomicron significantly increase FoxP3 expression and demethylates several CpG sites in FoxP3 promoter.•The activation of AHR might be involved in the effectiveness of B. thetaiotaomicron treatment for colitis.
Inflammatory bowel disease (IBD) is a form of nonspecific chronic intestinal inflammation associated with gut microbiome dysbiosis. Modulating the composition of the intestinal flora may be a viable means of alleviating such inflammatory pathology. Bacteroides thetaiotaomicron (B. thetaiotaomicron) is a symbiotic intestinal microbe that has been associated with IBD, although the mechanistic basis for this association remains to be clarified. In this present study, we determined that B. thetaiotaomicron can alleviate colonic inflammation through mechanisms associated with the modulation of tryptophan metabolism and T cell subsets within inflamed intestinal tissues. Specifically, we found that B. thetaiotaomicron promotes the preferential differentiation of anti-inflammatory Treg/Th2 cells while suppressing the relative differentiation of pro-inflammatory Th1/Th17 cells, thereby decreasing inflammation within the colon. At a molecular level, B. thetaiotaomicron treatment was linked to altered CpG methylation within the Foxp3 promoter that was associated with enhanced Treg cell functionality. In a murine dextran sulfate sodium (DSS) colitis model system, B. thetaiotaomicron increased the levels of the aryl hydrocarbon receptor (AHR) ligands indole metabolites-indole acetic acid (IAA) and indole propionic acid (IPA), thereby increasing AHR activation that is related to changes of transcription factor expression profiles within T cells. In summary, our data suggest that B. thetaiotaomicron can activate AHR and modulate CD4+ T cell differentiation profiles in a murine DSS colitis model system, suggesting that this bacterium may be of therapeutic relevance for the treatment of IBD. |
doi_str_mv | 10.1016/j.intimp.2020.107183 |
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Inflammatory bowel disease (IBD) is a form of nonspecific chronic intestinal inflammation associated with gut microbiome dysbiosis. Modulating the composition of the intestinal flora may be a viable means of alleviating such inflammatory pathology. Bacteroides thetaiotaomicron (B. thetaiotaomicron) is a symbiotic intestinal microbe that has been associated with IBD, although the mechanistic basis for this association remains to be clarified. In this present study, we determined that B. thetaiotaomicron can alleviate colonic inflammation through mechanisms associated with the modulation of tryptophan metabolism and T cell subsets within inflamed intestinal tissues. Specifically, we found that B. thetaiotaomicron promotes the preferential differentiation of anti-inflammatory Treg/Th2 cells while suppressing the relative differentiation of pro-inflammatory Th1/Th17 cells, thereby decreasing inflammation within the colon. At a molecular level, B. thetaiotaomicron treatment was linked to altered CpG methylation within the Foxp3 promoter that was associated with enhanced Treg cell functionality. In a murine dextran sulfate sodium (DSS) colitis model system, B. thetaiotaomicron increased the levels of the aryl hydrocarbon receptor (AHR) ligands indole metabolites-indole acetic acid (IAA) and indole propionic acid (IPA), thereby increasing AHR activation that is related to changes of transcription factor expression profiles within T cells. In summary, our data suggest that B. thetaiotaomicron can activate AHR and modulate CD4+ T cell differentiation profiles in a murine DSS colitis model system, suggesting that this bacterium may be of therapeutic relevance for the treatment of IBD.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2020.107183</identifier><identifier>PMID: 33229197</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Acetic acid ; Aromatic compounds ; Aryl hydrocarbon receptor ; Bacteroides thetaiotaomicron ; CD4 antigen ; Cell differentiation ; Colitis ; Colon ; CpG islands ; Dextran ; Dextran sulfate ; Dextrans ; Differentiation (biology) ; DNA methylation ; Dysbacteriosis ; Flora ; Foxp3 protein ; Helper cells ; Homeostasis ; Hydrocarbons ; Indoleacetic acid ; Inflammation ; Inflammatory bowel disease ; Inflammatory bowel diseases ; Intestinal microflora ; Intestine ; Lymphocytes ; Lymphocytes T ; Metabolism ; Metabolites ; Methylation ; Microbiomes ; Propionic acid ; Receptors ; Th1/Th2 ; Th17/Treg ; Tryptophan</subject><ispartof>International immunopharmacology, 2021-01, Vol.90, p.107183-107183, Article 107183</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright © 2020 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV Jan 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c320t-99fe9ea77bd150b4e860e7d60b3884ecd279ac9e1f6c846751a7588d06831183</citedby><cites>FETCH-LOGICAL-c320t-99fe9ea77bd150b4e860e7d60b3884ecd279ac9e1f6c846751a7588d06831183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S156757692033650X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33229197$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Keying</creatorcontrib><creatorcontrib>Hao, Zhenhua</creatorcontrib><creatorcontrib>Du, Jiying</creatorcontrib><creatorcontrib>Gao, Yimeng</creatorcontrib><creatorcontrib>Yang, Siyu</creatorcontrib><creatorcontrib>Zhou, Yanlin</creatorcontrib><title>Bacteroides thetaiotaomicron relieves colon inflammation by activating aryl hydrocarbon receptor and modulating CD4+T cell homeostasis</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>•B. thetaiotaomicron treatment ameliorates clinical signs of disease in DSS-induced colitis.•B. thetaiotaomicron enhanced the differentiation of Treg/Th2 cells and reduced the development of Th1/Th17 cells.•B. thetaiotaomicron significantly increase FoxP3 expression and demethylates several CpG sites in FoxP3 promoter.•The activation of AHR might be involved in the effectiveness of B. thetaiotaomicron treatment for colitis.
Inflammatory bowel disease (IBD) is a form of nonspecific chronic intestinal inflammation associated with gut microbiome dysbiosis. Modulating the composition of the intestinal flora may be a viable means of alleviating such inflammatory pathology. Bacteroides thetaiotaomicron (B. thetaiotaomicron) is a symbiotic intestinal microbe that has been associated with IBD, although the mechanistic basis for this association remains to be clarified. In this present study, we determined that B. thetaiotaomicron can alleviate colonic inflammation through mechanisms associated with the modulation of tryptophan metabolism and T cell subsets within inflamed intestinal tissues. Specifically, we found that B. thetaiotaomicron promotes the preferential differentiation of anti-inflammatory Treg/Th2 cells while suppressing the relative differentiation of pro-inflammatory Th1/Th17 cells, thereby decreasing inflammation within the colon. At a molecular level, B. thetaiotaomicron treatment was linked to altered CpG methylation within the Foxp3 promoter that was associated with enhanced Treg cell functionality. In a murine dextran sulfate sodium (DSS) colitis model system, B. thetaiotaomicron increased the levels of the aryl hydrocarbon receptor (AHR) ligands indole metabolites-indole acetic acid (IAA) and indole propionic acid (IPA), thereby increasing AHR activation that is related to changes of transcription factor expression profiles within T cells. In summary, our data suggest that B. thetaiotaomicron can activate AHR and modulate CD4+ T cell differentiation profiles in a murine DSS colitis model system, suggesting that this bacterium may be of therapeutic relevance for the treatment of IBD.</description><subject>Acetic acid</subject><subject>Aromatic compounds</subject><subject>Aryl hydrocarbon receptor</subject><subject>Bacteroides thetaiotaomicron</subject><subject>CD4 antigen</subject><subject>Cell differentiation</subject><subject>Colitis</subject><subject>Colon</subject><subject>CpG islands</subject><subject>Dextran</subject><subject>Dextran sulfate</subject><subject>Dextrans</subject><subject>Differentiation (biology)</subject><subject>DNA methylation</subject><subject>Dysbacteriosis</subject><subject>Flora</subject><subject>Foxp3 protein</subject><subject>Helper cells</subject><subject>Homeostasis</subject><subject>Hydrocarbons</subject><subject>Indoleacetic acid</subject><subject>Inflammation</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory bowel diseases</subject><subject>Intestinal microflora</subject><subject>Intestine</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Methylation</subject><subject>Microbiomes</subject><subject>Propionic acid</subject><subject>Receptors</subject><subject>Th1/Th2</subject><subject>Th17/Treg</subject><subject>Tryptophan</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kcuO1DAQRSMEYoaBP0AoEhsklMZOHD82SNA8pZHY9N5y7ArjVhw3ttNS_wDfTYUMLFiwsqt8brl0b1U9p2RHCeVvjjs_Fx9Ou5a0a0tQ2T2orqkUsqGC9A_x3nPR9IKrq-pJzkdCsM_o4-qq69pWUSWuq5_vjS2QoneQ63IHxfhYTAzepjjXCSYPZ3yxccLSz-NkQjDFYzFcapT6M1bz99qky1TfXVyK1qTht9TCqcRUm9nVIbpl2sD9B_b6UFuYEI8BYi4m-_y0ejSaKcOz-_OmOnz6eNh_aW6_ff66f3fb2K4lpVFqBAVGiMHRngwMJCcgHCdDJyUD61qhjFVAR24l46KnRvRSOsJlR9Gfm-rVNvaU4o8FctHB53UXM0Ncsm4ZZ5QpIQWiL_9Bj3FJMy6HlKKcdi1dKbZRaFfOCUZ9Sj6gGZoSvcakj3qLSa8x6S0mlL24H74MAdxf0Z9cEHi7AYBmnD0kna2H2YLzaGzRLvr___ALxlKnfQ</recordid><startdate>202101</startdate><enddate>202101</enddate><creator>Li, Keying</creator><creator>Hao, Zhenhua</creator><creator>Du, Jiying</creator><creator>Gao, Yimeng</creator><creator>Yang, Siyu</creator><creator>Zhou, Yanlin</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T5</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>202101</creationdate><title>Bacteroides thetaiotaomicron relieves colon inflammation by activating aryl hydrocarbon receptor and modulating CD4+T cell homeostasis</title><author>Li, Keying ; Hao, Zhenhua ; Du, Jiying ; Gao, Yimeng ; Yang, Siyu ; Zhou, Yanlin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c320t-99fe9ea77bd150b4e860e7d60b3884ecd279ac9e1f6c846751a7588d06831183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acetic acid</topic><topic>Aromatic compounds</topic><topic>Aryl hydrocarbon receptor</topic><topic>Bacteroides thetaiotaomicron</topic><topic>CD4 antigen</topic><topic>Cell differentiation</topic><topic>Colitis</topic><topic>Colon</topic><topic>CpG islands</topic><topic>Dextran</topic><topic>Dextran sulfate</topic><topic>Dextrans</topic><topic>Differentiation (biology)</topic><topic>DNA methylation</topic><topic>Dysbacteriosis</topic><topic>Flora</topic><topic>Foxp3 protein</topic><topic>Helper cells</topic><topic>Homeostasis</topic><topic>Hydrocarbons</topic><topic>Indoleacetic acid</topic><topic>Inflammation</topic><topic>Inflammatory bowel disease</topic><topic>Inflammatory bowel diseases</topic><topic>Intestinal microflora</topic><topic>Intestine</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Methylation</topic><topic>Microbiomes</topic><topic>Propionic acid</topic><topic>Receptors</topic><topic>Th1/Th2</topic><topic>Th17/Treg</topic><topic>Tryptophan</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Keying</creatorcontrib><creatorcontrib>Hao, Zhenhua</creatorcontrib><creatorcontrib>Du, Jiying</creatorcontrib><creatorcontrib>Gao, Yimeng</creatorcontrib><creatorcontrib>Yang, Siyu</creatorcontrib><creatorcontrib>Zhou, Yanlin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Keying</au><au>Hao, Zhenhua</au><au>Du, Jiying</au><au>Gao, Yimeng</au><au>Yang, Siyu</au><au>Zhou, Yanlin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bacteroides thetaiotaomicron relieves colon inflammation by activating aryl hydrocarbon receptor and modulating CD4+T cell homeostasis</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2021-01</date><risdate>2021</risdate><volume>90</volume><spage>107183</spage><epage>107183</epage><pages>107183-107183</pages><artnum>107183</artnum><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>•B. thetaiotaomicron treatment ameliorates clinical signs of disease in DSS-induced colitis.•B. thetaiotaomicron enhanced the differentiation of Treg/Th2 cells and reduced the development of Th1/Th17 cells.•B. thetaiotaomicron significantly increase FoxP3 expression and demethylates several CpG sites in FoxP3 promoter.•The activation of AHR might be involved in the effectiveness of B. thetaiotaomicron treatment for colitis.
Inflammatory bowel disease (IBD) is a form of nonspecific chronic intestinal inflammation associated with gut microbiome dysbiosis. Modulating the composition of the intestinal flora may be a viable means of alleviating such inflammatory pathology. Bacteroides thetaiotaomicron (B. thetaiotaomicron) is a symbiotic intestinal microbe that has been associated with IBD, although the mechanistic basis for this association remains to be clarified. In this present study, we determined that B. thetaiotaomicron can alleviate colonic inflammation through mechanisms associated with the modulation of tryptophan metabolism and T cell subsets within inflamed intestinal tissues. Specifically, we found that B. thetaiotaomicron promotes the preferential differentiation of anti-inflammatory Treg/Th2 cells while suppressing the relative differentiation of pro-inflammatory Th1/Th17 cells, thereby decreasing inflammation within the colon. At a molecular level, B. thetaiotaomicron treatment was linked to altered CpG methylation within the Foxp3 promoter that was associated with enhanced Treg cell functionality. In a murine dextran sulfate sodium (DSS) colitis model system, B. thetaiotaomicron increased the levels of the aryl hydrocarbon receptor (AHR) ligands indole metabolites-indole acetic acid (IAA) and indole propionic acid (IPA), thereby increasing AHR activation that is related to changes of transcription factor expression profiles within T cells. In summary, our data suggest that B. thetaiotaomicron can activate AHR and modulate CD4+ T cell differentiation profiles in a murine DSS colitis model system, suggesting that this bacterium may be of therapeutic relevance for the treatment of IBD.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>33229197</pmid><doi>10.1016/j.intimp.2020.107183</doi><tpages>1</tpages></addata></record> |
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subjects | Acetic acid Aromatic compounds Aryl hydrocarbon receptor Bacteroides thetaiotaomicron CD4 antigen Cell differentiation Colitis Colon CpG islands Dextran Dextran sulfate Dextrans Differentiation (biology) DNA methylation Dysbacteriosis Flora Foxp3 protein Helper cells Homeostasis Hydrocarbons Indoleacetic acid Inflammation Inflammatory bowel disease Inflammatory bowel diseases Intestinal microflora Intestine Lymphocytes Lymphocytes T Metabolism Metabolites Methylation Microbiomes Propionic acid Receptors Th1/Th2 Th17/Treg Tryptophan |
title | Bacteroides thetaiotaomicron relieves colon inflammation by activating aryl hydrocarbon receptor and modulating CD4+T cell homeostasis |
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