MicroRNAs Targeting Programmed Cell Death Protein 1 (PD-1) Promote Natural Killer Cell Exhaustion in Rheumatoid Arthritis

流式细胞术 白细胞介素21 外周血单个核细胞 小RNA Janus激酶3 免疫学 下调和上调 细胞 自然杀伤细胞 淋巴因子激活杀伤细胞 医学 生物 癌症研究 免疫系统 细胞毒性T细胞 T细胞 体外 基因 生物化学 遗传学
作者
Maryam Hemmatzadeh,Elham Ahangar Parvin,Alireza Ghanavatinejad,Narges Rostami,Mehrzad Hajaliloo,Navid Shomali,Hamed Mohammadi,Farhad Jadidi-Niaragh
出处
期刊:Iranian Journal of Allergy Asthma and Immunology [Knowledge E]
标识
DOI:10.18502/ijaai.v21i6.11524
摘要

Natural killer (NK) cells play a role in the pathogenesis of rheumatoid arthritis (RA). Upregulated levels of programmed cell death protein 1 (PD-1) is a sign of exhausted NK cells that could be regulated by microRNAs (miRNAs). In this investigation, we determined PD‑1 expression on NK cells (as a representation of NK cell exhaustion) in RA patients and evaluated if miRNAs are involved in the modulation of PD-1 expression in NK cells. Peripheral blood specimens were obtained from 40 RA patients and 20 healthy subjects. NK cells were isolated by negative selection from a pool of peripheral blood mononuclear cells. The frequency of PD-1–expressing NK cells and the expression of PD-1 on NK cells were analyzed by flow cytometry. Real-time PCR was used to measure the expression levels of PD-1 mRNA and miRNAs in the NK cells. The percentage of the PD-1–expressing NK cells and Mean fluorescence intensity (MFI) of PD-1 expression on the NK cells were significantly higher in the RA cases compared to the controls. The mRNA expression of PD-1 was significantly upregulated in NK cells from RA patients compared to healthy subjects. The expression levels of miR-28, miR-138, and miR-4717 were significantly downregulated in the NK cells from RA patients compared to the healthy group. In RA, miRNAs probably regulate the NK cell exhaustion process through driving PD-1 expression.

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