{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Lee JS"],"funding":["BLRD VA","NIDDK NIH HHS"],"pagination":["6039-6051"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5912467"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["293(16)"],"pubmed_abstract":["Intestinal epithelial cells form a selectively permeable barrier to protect colon tissues from luminal microbiota and antigens and to mediate nutrient, fluid, and waste flux in the intestinal tract. Dysregulation of the epithelial cell barrier coincides with profound shifts in metabolic energy, especially in the colon, which exists in an energetically depleting state of physiological hypoxia. However, studies that systematically examine energy flux and adenylate metabolism during intestinal epithelial barrier development and restoration after disruption are lacking. Here, to delineate barrier-related energy flux, we developed an HPLC-based profiling method to track changes in energy flux and adenylate metabolites during barrier development and restoration. Cultured epithelia exhibited pooling of phosphocreatine and maintained ATP during barrier development. EDTA-induced epithelial barrier disruption revealed that hypoxanthine levels correlated with barrier resistance. Further studies uncovered that hypoxanthine supplementation improves barrier function and wound healing and that hypoxanthine appears to do so by increasing intracellular ATP, which improved cytoskeletal G- to F-actin polymerization. Hypoxanthine supplementation increased the adenylate energy charge in the murine colon, indicating potential to regulate adenylate energy charge-mediated metabolism in intestinal epithelial cells. Moreover, experiments in a murine colitis model disclosed that hypoxanthine loss during active inflammation correlates with markers of disease severity. In summary, our results indicate that hypoxanthine modulates energy metabolism in intestinal epithelial cells and is critical for intestinal barrier function."],"journal":["The Journal of biological chemistry"],"pubmed_title":["Hypoxanthine is a checkpoint stress metabolite in colonic epithelial energy modulation and barrier function."],"pmcid":["PMC5912467"],"funding_grant_id":["P30 DK048520","R37 DK050189","R29 DK050189","I01 BX002182","R01 DK050189","R01 DK095491","R01 DK103712","R01 DK104713"],"pubmed_authors":["Lee JS","Colgan SP","Wang RX","Lanis JM","Battista KD","Glover LE","Alexeev EE"],"additional_accession":[]},"is_claimable":false,"name":"Hypoxanthine is a checkpoint stress metabolite in colonic epithelial energy modulation and barrier function.","description":"Intestinal epithelial cells form a selectively permeable barrier to protect colon tissues from luminal microbiota and antigens and to mediate nutrient, fluid, and waste flux in the intestinal tract. Dysregulation of the epithelial cell barrier coincides with profound shifts in metabolic energy, especially in the colon, which exists in an energetically depleting state of physiological hypoxia. However, studies that systematically examine energy flux and adenylate metabolism during intestinal epithelial barrier development and restoration after disruption are lacking. Here, to delineate barrier-related energy flux, we developed an HPLC-based profiling method to track changes in energy flux and adenylate metabolites during barrier development and restoration. Cultured epithelia exhibited pooling of phosphocreatine and maintained ATP during barrier development. EDTA-induced epithelial barrier disruption revealed that hypoxanthine levels correlated with barrier resistance. Further studies uncovered that hypoxanthine supplementation improves barrier function and wound healing and that hypoxanthine appears to do so by increasing intracellular ATP, which improved cytoskeletal G- to F-actin polymerization. Hypoxanthine supplementation increased the adenylate energy charge in the murine colon, indicating potential to regulate adenylate energy charge-mediated metabolism in intestinal epithelial cells. Moreover, experiments in a murine colitis model disclosed that hypoxanthine loss during active inflammation correlates with markers of disease severity. In summary, our results indicate that hypoxanthine modulates energy metabolism in intestinal epithelial cells and is critical for intestinal barrier function.","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018 Apr","modification":"2021-02-21T08:13:02Z","creation":"2019-06-06T19:23:06Z"},"accession":"S-EPMC5912467","cross_references":{"pubmed":["29487135"],"doi":["10.1074/jbc.RA117.000269","10.1074/jbc.ra117.000269"]}}