锰通过 cGAS-STING 介导的 UTX 表达增强自然杀伤细胞功能

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
MedComm Pub Date : 2024-08-28 DOI:10.1002/mco2.683
Qianyi Ming, Jiejie Liu, Zijian Lv, Tiance Wang, Runjia Fan, Yan Zhang, Meixia Chen, Yingli Sun, Weidong Han, Qian Mei
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引用次数: 0

摘要

自然杀伤(NK)细胞在先天性免疫和激活适应性免疫中发挥着至关重要的作用。Mn2+ 对环状 GMP-AMP(cGAS)-干扰素基因刺激器(STING 信号转导)的激活作用已广为人知,但其对 NK 细胞的作用却仍然难以捉摸。在这项研究中,我们发现了锰(Mn2+)在激活 NK 细胞中的重要作用。Mn2+ 可直接增强 NK 细胞的细胞毒性,促进 NK 细胞分泌细胞因子,从而激活 CD8+ T 细胞,增强其抗肿瘤活性。此外,Mn2+ 还能同时激活 NK 细胞固有的 cGAS 和 STING,从而增强 X 染色体上无处不在的转录四肽重复(UTX)的表达,促进 NK 细胞的反应性。我们的研究结果有助于更广泛地理解 cGAS-STING 如何调控 NK 细胞。作为 cGAS-STING 的强效激动剂,Mn2+ 为基于 NK 细胞的癌症免疫疗法提供了一种前景广阔的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Manganese boosts natural killer cell function via cGAS–STING mediated UTX expression

Manganese boosts natural killer cell function via cGAS–STING mediated UTX expression

Natural killer (NK) cells play a crucial role in both innate immunity and the activation of adaptive immunity. The activating effect of Mn2+ on cyclic GMP-AMP(cGAS)–stimulator of interferon genes (STING signaling has been well known, but its effect on NK cells remains elusive. In this study, we identified the vital role of manganese (Mn2+) in NK cell activation. Mn2+ directly boosts cytotoxicity of NK cells and promotes the cytokine secretion by NK cells, thereby activating CD8+ T cells and enhancing their antitumor activity. Furthermore, Mn2+ can simultaneously activate NK-cell intrinsic cGAS and STING and consequently augment the expression of ubiquitously transcribed tetratricopeptide repeat on chromosome X (UTX to promote the responsiveness of NK cells. Our results contribute to a broader comprehension of how cGAS–STING regulates NK cells. As a potent agonist of cGAS–STING, Mn2+ provides a promising option for NK cell-based immunotherapy of cancers.

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CiteScore
6.70
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