Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Tianjin, China.
Tianjin Neurological Institute, Key Laboratory of Post-neurotrauma Neuro-Repair and Regeneration in Central Nervous System, Ministry of Education and Tianjin City, Tianjin, China.
Front Immunol. 2020 May 14;11:759. doi: 10.3389/fimmu.2020.00759. eCollection 2020.
Brain ischemia induces systemic immunosuppression and increases a host's susceptibility to infection. MicroRNAs (miRNAs) are molecular switches in immune cells, but the alterations of miRNAs in human immune cells in response to brain ischemia and their impact on immune defense remain elusive. Natural killer (NK) cells are critical for early host defenses against pathogens. In this study, we identified reduced counts, cytokine production, and cytotoxicity in human peripheral blood NK cells obtained from patients with acute ischemic stroke. The extent of NK cell loss of number and activity was associated with infarct volume. MicroRNA sequencing analysis revealed that brain ischemia significantly altered miRNA expression profiles in circulating NK cells, in which miRNA-451a and miRNA-122-5p were dramatically upregulated. Importantly, inhibition of miR-451a or miR-122-5p augmented the expression of activation-associated receptors in NK cells. These results provide the first evidence that brain ischemia alters miRNA signatures in human NK cells.
脑缺血诱导全身免疫抑制,增加宿主易感性感染。MicroRNAs (miRNAs) 是免疫细胞中的分子开关,但人类免疫细胞对脑缺血的反应中 miRNAs 的变化及其对免疫防御的影响仍不清楚。自然杀伤 (NK) 细胞是宿主对病原体早期防御的关键。在这项研究中,我们发现从急性缺血性脑卒中患者外周血中获得的 NK 细胞数量减少、细胞因子产生减少和细胞毒性降低。NK 细胞数量和活性的丧失程度与梗死体积相关。miRNA 测序分析显示,脑缺血显著改变了循环 NK 细胞中的 miRNA 表达谱,其中 miRNA-451a 和 miRNA-122-5p 显著上调。重要的是,抑制 miR-451a 或 miR-122-5p 可增强 NK 细胞中激活相关受体的表达。这些结果首次提供了脑缺血改变人 NK 细胞中 miRNA 特征的证据。