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本文引用的文献

1
Gene Regulatory Programs Conferring Phenotypic Identities to Human NK Cells.基因调控程序赋予人类自然杀伤细胞表型特征。
Cell. 2019 Jan 10;176(1-2):348-360.e12. doi: 10.1016/j.cell.2018.11.045. Epub 2018 Dec 27.
2
MicroRNA regulation of type 2 innate lymphoid cell homeostasis and function in allergic inflammation.微小RNA对2型固有淋巴细胞稳态及在过敏性炎症中功能的调控
J Exp Med. 2017 Dec 4;214(12):3627-3643. doi: 10.1084/jem.20170545. Epub 2017 Nov 9.
3
ILC1 Confer Early Host Protection at Initial Sites of Viral Infection.ILC1在病毒感染的初始部位赋予早期宿主保护作用。
Cell. 2017 Nov 2;171(4):795-808.e12. doi: 10.1016/j.cell.2017.09.052. Epub 2017 Oct 19.
4
Rac1 functions downstream of miR-142 in regulation of erythropoiesis.Rac1在红细胞生成的调控中作用于miR-142的下游。
Haematologica. 2017 Dec;102(12):e476-e480. doi: 10.3324/haematol.2017.171736. Epub 2017 Sep 14.
5
SMAD4 impedes the conversion of NK cells into ILC1-like cells by curtailing non-canonical TGF-β signaling.SMAD4通过抑制非经典TGF-β信号传导来阻碍自然杀伤细胞向ILC1样细胞的转化。
Nat Immunol. 2017 Sep;18(9):995-1003. doi: 10.1038/ni.3809. Epub 2017 Jul 31.
6
Tumor immunoevasion by the conversion of effector NK cells into type 1 innate lymphoid cells.效应 NK 细胞向 1 型先天淋巴样细胞的转化导致肿瘤免疫逃逸。
Nat Immunol. 2017 Sep;18(9):1004-1015. doi: 10.1038/ni.3800. Epub 2017 Jul 31.
7
Inflammatory Th17 Cells Express Integrin αvβ3 for Pathogenic Function.炎性Th17细胞表达整合素αvβ3以发挥致病功能。
Cell Rep. 2016 Aug 2;16(5):1339-1351. doi: 10.1016/j.celrep.2016.06.065. Epub 2016 Jul 21.
8
CIS is a potent checkpoint in NK cell-mediated tumor immunity.CIS 是 NK 细胞介导的肿瘤免疫中的一个有效检查点。
Nat Immunol. 2016 Jul;17(7):816-24. doi: 10.1038/ni.3470. Epub 2016 May 23.
9
Transforming Growth Factor-β Signaling Guides the Differentiation of Innate Lymphoid Cells in Salivary Glands.转化生长因子-β信号传导指导唾液腺中固有淋巴细胞的分化。
Immunity. 2016 May 17;44(5):1127-39. doi: 10.1016/j.immuni.2016.03.007. Epub 2016 May 3.
10
Transcriptional and post-transcriptional regulation of NK cell development and function.自然杀伤细胞发育与功能的转录及转录后调控
Clin Immunol. 2017 Apr;177:60-69. doi: 10.1016/j.clim.2016.03.003. Epub 2016 Mar 3.

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.

DOI:10.1016/j.immuni.2019.06.016
PMID:31402259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6750984/
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。