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Enhancement of the gut barrier integrity by a microbial metabolite through the Nrf2 pathway

Rajbir SinghDepartment of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USASandeep ChandrashekharappaInstitute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus, Bangalore, Karnataka, 560065, IndiaSobha R. BodduluriDepartment of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USABecca V. BabyDepartment of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USABindu HegdeDepartment of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USANiranjan G. KotlaInstitute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus, Bangalore, Karnataka, 560065, IndiaAnkita HiwaleInstitute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus, Bangalore, Karnataka, 560065, IndiaTaslimarif SaiyedParesh D. PatelMatam Vijay–KumarDepartment of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, 43614, USAMorgan G. I. LangilleDepartment of Pharmacology, Dalhousie University, Halifax, B3H 4R2, Nova Scotia, CanadaGavin M. DouglasDepartment of Pharmacology, Dalhousie University, Halifax, B3H 4R2, Nova Scotia, CanadaXi ChengDepartment of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, 43614, USAEric C. RouchkaComputer Engineering and Computer Science, Kentucky Biomedical Research Infrastructure Network, University of Louisville, Louisville, KY, 40202, USASabine WaigelDepartment of Medicine, University of Louisville, Louisville, KY, 40202, USAGerald W. DrydenDepartment of Medicine, University of Louisville, Louisville, KY, 40202, USAHouda AlatassiDepartment of Pathology, University of Louisville, Louisville, KY, 40202, USAHuang-Ge ZhangDepartment of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USABodduluri HaribabuDepartment of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USAPraveen Kumar VemulaInstitute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus, Bangalore, Karnataka, 560065, India. [email protected]Venkatakrishna R. JalaDepartment of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USA. [email protected]
2019en
ABI

Аннотация

The importance of gut microbiota in human health and pathophysiology is undisputable. Despite the abundance of metagenomics data, the functional dynamics of gut microbiota in human health and disease remain elusive. Urolithin A (UroA), a major microbial metabolite derived from polyphenolics of berries and pomegranate fruits displays anti-inflammatory, anti-oxidative, and anti-ageing activities. Here, we show that UroA and its potent synthetic analogue (UAS03) significantly enhance gut barrier function and inhibit unwarranted inflammation. We demonstrate that UroA and UAS03 exert their barrier functions through activation of aryl hydrocarbon receptor (AhR)- nuclear factor erythroid 2-related factor 2 (Nrf2)-dependent pathways to upregulate epithelial tight junction proteins. Importantly, treatment with these compounds attenuated colitis in pre-clinical models by remedying barrier dysfunction in addition to anti-inflammatory activities. Cumulatively, the results highlight how microbial metabolites provide two-pronged beneficial activities at gut epithelium by enhancing barrier functions and reducing inflammation to protect from colonic diseases.

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