MicroRNA-221 and -222 modulate intestinal inflammatory Th17 cell response as negative feedback regulators downstream of interleukin-23

microRNA-221 和 -222 作为白细胞介素-23 下游的负反馈调节因子,调控肠道炎症性 Th17 细胞反应。

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作者:Yohei Mikami ,Rachael L Philips ,Giuseppe Sciumè ,Franziska Petermann ,Françoise Meylan ,Hiroyuki Nagashima ,Chen Yao ,Fred P Davis ,Stephen R Brooks ,Hong-Wei Sun ,Hayato Takahashi ,Amanda C Poholek ,Han-Yu Shih ,Behdad Afzali ,Stefan A Muljo ,Markus Hafner ,Yuka Kanno ,John J O'Shea

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.

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