School of Immunology and Microbial Sciences, King's College London, London, United Kingdom.
Centre for Host-Microbiome Interactions, King's College London, London, United Kingdom.
J Immunol. 2021 Jun 1;206(11):2725-2739. doi: 10.4049/jimmunol.2000647. Epub 2021 May 21.
Innate lymphoid cells are central to the regulation of immunity at mucosal barrier sites, with group 2 innate lymphoid cells (ILC2s) being particularly important in type 2 immunity. In this study, we demonstrate that microRNA(miR)-142 plays a critical, cell-intrinsic role in the homeostasis and function of ILC2s. Mice deficient for miR-142 expression demonstrate an ILC2 progenitor-biased development in the bone marrow, and along with peripheral ILC2s at mucosal sites, these cells display a greatly altered phenotype based on surface marker expression. ILC2 proliferative and effector functions are severely dysfunctional following infection, revealing a critical role for miR-142 isoforms in ILC2-mediated immune responses. Mechanistically, and expression are regulated by miR-142 isoforms in ILC2s, impacting ILC2 phenotypes as well as the proliferative and effector capacity of these cells. The identification of these novel pathways opens potential new avenues to modulate ILC2-dependent immune functions.
先天淋巴细胞是黏膜屏障部位免疫调节的核心,其中 2 型固有淋巴细胞(ILC2)在 2 型免疫中尤为重要。在这项研究中,我们证明了 microRNA(miR)-142 在 ILC2 的稳态和功能中发挥着关键的、细胞内在的作用。缺乏 miR-142 表达的小鼠在骨髓中表现出 ILC2 祖细胞偏向性发育,并且与黏膜部位的外周 ILC2 一起,这些细胞基于表面标志物表达显示出极大改变的表型。感染后,ILC2 的增殖和效应功能严重失调,这揭示了 miR-142 异构体在 ILC2 介导的免疫反应中的关键作用。在机制上, 和 的表达受 ILC2 中的 miR-142 异构体调节,影响 ILC2 的表型以及这些细胞的增殖和效应能力。这些新途径的鉴定为调节 ILC2 依赖性免疫功能开辟了潜在的新途径。