| Literature DB >> 33657395 |
Yohei Mikami1, Rachael L Philips2, Giuseppe Sciumè1, Franziska Petermann1, Françoise Meylan1, Hiroyuki Nagashima1, Chen Yao1, Fred P Davis1, Stephen R Brooks3, Hong-Wei Sun3, Hayato Takahashi1, Amanda C Poholek1, Han-Yu Shih1, Behdad Afzali1, Stefan A Muljo4, Markus Hafner5, Yuka Kanno6, John J O'Shea7.
Abstract
MicroRNAs are important regulators of immune responses. Here, we show miR-221 and miR-222 modulate the intestinal Th17 cell response. Expression of miR-221 and miR-222 was induced by proinflammatory cytokines and repressed by the cytokine TGF-β. Molecular targets of miR-221 and miR-222 included Maf and Il23r, and loss of miR-221 and miR-222 expression shifted the transcriptomic spectrum of intestinal Th17 cells to a proinflammatory signature. Although the loss of miR-221 and miR-222 was tolerated for maintaining intestinal Th17 cell homeostasis in healthy mice, Th17 cells lacking miR-221 and miR-222 expanded more efficiently in response to IL-23. Both global and T cell-specific deletion of miR-221 and miR-222 rendered mice prone to mucosal barrier damage. Collectively, these findings demonstrate that miR-221 and miR-222 are an integral part of intestinal Th17 cell response that are induced after IL-23 stimulation to constrain the magnitude of proinflammatory response. Published by Elsevier Inc.Entities:
Keywords: IL23r; Maf; Th17; helper T cells; intestine; miR-221; miR-222; miRNA; mucosal barrier damage; negative feedback
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Year: 2021 PMID: 33657395 PMCID: PMC8025838 DOI: 10.1016/j.immuni.2021.02.015
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745