{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Zhu L"],"funding":["Ministry of Science and Technology of the People’s Republic of China","National Natural Science Foundation of China","Science and Technology Department of Zhejiang Province"],"pagination":["2790"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10185671"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["14(1)"],"pubmed_abstract":["Iron deficiencies are the most common nonenteric syndromes observed in patients with inflammatory bowel disease, but little is known about their impacts on immune tolerance. Here we show that homeostasis of regulatory T cells in the intestine was dependent on high cellular iron levels, which were fostered by pentanoate, a short-chain fatty acid produced by intestinal microbiota. Iron deficiencies in Treg caused by the depletion of Transferrin receptor 1, a major iron transporter, result in the abrogation of Treg in the intestine and lethal autoimmune disease. Transferrin receptor 1 is required for differentiation of c-Maf<sup>+</sup> Treg, major constituents of intestinal Treg. Mechanistically, iron enhances the translation of HIF-2α mRNA, and HIF-2α in turn induces c-Maf expression. Impor"],"journal":["Nature communications"],"pubmed_title":["Microbiota-assisted iron uptake promotes immune tolerance in the intestine."],"pmcid":["PMC10185671"],"funding_grant_id":["2022SDXHDX0002","31870927, 32025016, 81671552, 81830078","2022YFA0807300,2018YFA0107500, 2018YFA0801400"],"pubmed_authors":["Li G","Peng Y","Zheng J","Zhu L","Liang Z","Deng K","Qi T","Yu J","Chang X","Song Y"],"additional_accession":[]},"is_claimable":false,"name":"Microbiota-assisted iron uptake promotes immune tolerance in the intestine.","description":"Iron deficiencies are the most common nonenteric syndromes observed in patients with inflammatory bowel disease, but little is known about their impacts on immune tolerance. Here we show that homeostasis of regulatory T cells in the intestine was dependent on high cellular iron levels, which were fostered by pentanoate, a short-chain fatty acid produced by intestinal microbiota. Iron deficiencies in Treg caused by the depletion of Transferrin receptor 1, a major iron transporter, result in the abrogation of Treg in the intestine and lethal autoimmune disease. Transferrin receptor 1 is required for differentiation of c-Maf<sup>+</sup> Treg, major constituents of intestinal Treg. Mechanistically, iron enhances the translation of HIF-2α mRNA, and HIF-2α in turn induces c-Maf expression. Impor","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 May","modification":"2026-07-14T21:16:29.143Z","creation":"2025-04-05T10:54:19.143Z"},"accession":"S-EPMC10185671","cross_references":{"pubmed":["37188703"],"doi":["10.1038/s41467-023-38444-2"]}}