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miRNA-142 对 1 型固有淋巴细胞的稳态和功能至关重要。

MicroRNA-142 Is Critical for the Homeostasis and Function of Type 1 Innate Lymphoid Cells.

机构信息

Department of Medicine, Division of Oncology, Washington University School of Medicine, Saint Louis, MO, USA.

Division of Hematology and Oncology, University of Michigan, Ann Arbor, MI, USA.

出版信息

Immunity. 2019 Sep 17;51(3):479-490.e6. doi: 10.1016/j.immuni.2019.06.016. Epub 2019 Aug 8.

Abstract

Natural killer (NK) cells are cytotoxic type 1 innate lymphoid cells (ILCs) that defend against viruses and mediate anti-tumor responses, yet mechanisms controlling their development and function remain incompletely understood. We hypothesized that the abundantly expressed microRNA-142 (miR-142) is a critical regulator of type 1 ILC biology. Interleukin-15 (IL-15) signaling induced miR-142 expression, whereas global and ILC-specific miR-142-deficient mice exhibited a cell-intrinsic loss of NK cells. Death of NK cells resulted from diminished IL-15 receptor signaling within miR-142-deficient mice, likely via reduced suppressor of cytokine signaling-1 (Socs1) regulation by miR-142-5p. ILCs persisting in Mir142 mice demonstrated increased expression of the miR-142-3p target αV integrin, which supported their survival. Global miR-142-deficient mice exhibited an expansion of ILC1-like cells concurrent with increased transforming growth factor-β (TGF-β) signaling. Further, miR-142-deficient mice had reduced NK-cell-dependent function and increased susceptibility to murine cytomegalovirus (MCMV) infection. Thus, miR-142 critically integrates environmental cues for proper type 1 ILC homeostasis and defense against viral infection.

摘要

自然杀伤 (NK) 细胞是细胞毒性的 1 型固有淋巴细胞 (ILC),可抵抗病毒并介导抗肿瘤反应,但控制其发育和功能的机制仍不完全清楚。我们假设丰富表达的 microRNA-142 (miR-142) 是 1 型 ILC 生物学的关键调节因子。白细胞介素-15 (IL-15) 信号诱导 miR-142 表达,而全身和 ILC 特异性 miR-142 缺陷小鼠表现出 NK 细胞的细胞内在缺失。NK 细胞的死亡是由于 miR-142 缺陷小鼠中 IL-15 受体信号的减少,可能是由于 miR-142-5p 对细胞因子信号转导抑制因子 1 (Socs1) 的调节减少所致。在 Mir142 小鼠中持续存在的 ILC 表现出 miR-142-3p 靶标 αV 整合素的表达增加,这支持了它们的存活。全身 miR-142 缺陷小鼠表现出 ILC1 样细胞的扩增,同时 TGF-β 信号转导增加。此外,miR-142 缺陷小鼠的 NK 细胞依赖性功能降低,对小鼠巨细胞病毒 (MCMV) 感染的易感性增加。因此,miR-142 对于适当的 1 型 ILC 稳态和防御病毒感染至关重要。

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