Cheng Lin, Liang Xintong, Qian Long, Luo Chaoyin, Li Dongxu
Department of Rheumatology and Immunology, The Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230001, P.R. China.
Exp Ther Med. 2021 Oct;22(4):1110. doi: 10.3892/etm.2021.10544. Epub 2021 Aug 3.
The present study aimed to investigate the association between the single-nucleotide polymorphisms (SNPs) rs4612666 and rs10754558 in the NOD-, LRR- and pyrin domain-containing protein 3 (NLRP3) gene and the susceptibility to rheumatoid arthritis (RA) in a Han Chinese population. mRNA expression of NLRP3, apoptosis-associated speck-like protein (ASC), and caspase-1 were determined in peripheral blood mononuclear cells (PBMCs) and neutrophils using reverse-transcription quantitative PCR. The results demonstrated that the C allele at rs4612666 locus and the G allele at rs10754558 locus were associated with significantly increased risk of RA. A statistical significance was also revealed in the dominant model (CC+CT vs. TT: OR=1.549; 95% CI=1.120-2.144; and GG + GC vs. CC: OR=2.000; 95% CI=1.529-2.616; P<0.05). Additionally, the mRNA expression of NLRP3, ASC and caspase-1 in PBMCs and neutrophils derived from patients with RA were significantly upregulated compared with the controls. Furthermore, the mRNA levels of NLRP3, ASC and caspase-1 in PBMCs and neutrophils from patients with active RA were notably increased compared with patients in remission. NLRP3 expression was positively correlated with the levels of C-reaction protein, erythrocyte sedimentation rate and disease activity score of 28 joint counts. Overall, the current study indicated that the NLRP3 rs4612666 and rs10754558 loci were associated with susceptibility to RA. In addition, the results of the present study demonstrated that the high expression of NLRP3 could serve a critical role in the pathogenesis of RA.
本研究旨在探讨含核苷酸结合寡聚化结构域样受体蛋白3(NLRP3)基因的单核苷酸多态性(SNP)rs4612666和rs10754558与汉族人群类风湿关节炎(RA)易感性之间的关联。采用逆转录定量PCR法检测外周血单个核细胞(PBMC)和中性粒细胞中NLRP3、凋亡相关斑点样蛋白(ASC)和半胱天冬酶-1的mRNA表达。结果表明,rs4612666位点的C等位基因和rs10754558位点的G等位基因与RA风险显著增加相关。显性模型也显示出统计学意义(CC + CT与TT相比:OR = 1.549;95%CI = 1.120 - 2.144;GG + GC与CC相比:OR = 2.000;95%CI = 1.529 - 2.616;P < 0.05)。此外,与对照组相比,RA患者PBMC和中性粒细胞中NLRP3、ASC和半胱天冬酶-1的mRNA表达显著上调。此外,与缓解期患者相比,活动期RA患者PBMC和中性粒细胞中NLRP3、ASC和半胱天冬酶-1的mRNA水平显著升高。NLRP3表达与C反应蛋白水平、红细胞沉降率和28个关节计数的疾病活动评分呈正相关。总体而言,本研究表明NLRP3 rs4612666和rs10754558位点与RA易感性相关。此外,本研究结果表明NLRP3的高表达在RA发病机制中起关键作用。