Microbiota-assisted iron uptake promotes immune tolerance in the intestine

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 fo...

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Published inNature communications Vol. 14; no. 1; pp. 2790 - 16
Main Authors Zhu, Lizhen, Li, Geng, Liang, Zhixin, Qi, Tuan, Deng, Kui, Yu, Jiancheng, Peng, Yue, Zheng, Jusheng, Song, Yan, Chang, Xing
Format Journal Article
LanguageEnglish
Published England Nature Publishing Group 15.05.2023
Nature Publishing Group UK
Nature Portfolio
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Summary: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 Treg, major constituents of intestinal Treg. Mechanistically, iron enhances the translation of HIF-2α mRNA, and HIF-2α in turn induces c-Maf expression. Importantly, microbiota-produced pentanoate promotes iron uptake and Treg differentiation in the intestine. This subsequently restores immune tolerance and ameliorated iron deficiencies in mice with colitis. Our results thus reveal an association between nutrient uptake and immune tolerance in the intestine.
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ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-023-38444-2