Neutrophil extracellular traps in rheumatoid arthritis and periodontitis: Contribution of PADI4 gene polymorphisms

中性粒细胞胞外陷阱 牙周炎 单核苷酸多态性 类风湿性关节炎 单倍型 髓过氧化物酶 免疫学 牙龈卟啉单胞菌 医学 关节炎 炎症 基因型 基因 生物 内科学 遗传学
作者
Sicília Rezende Oliveira,José Alcides Almeida de Arruda,Ayda Henriques Schneider,Larissa Marques Bemquerer,Rayssa Maria Soalheiro de Souza,Paula Barbim,Gustavo Henrique Mattos Pereira,Débora Cerqueira Calderaro,Caio Cavalcante Machado,Sandra Yasuyo Fukada,Paula Rocha Moreira,Renê Donizeti Ribeiro de Oliveira,Paulo Louzada‐Júnior,Lucas Guimarães Abreu,Fernando Q. Cunha,Tarcı́lia Aparecida Silva
出处
期刊:Journal of Clinical Periodontology [Wiley]
卷期号:51 (4): 452-463 被引量:1
标识
DOI:10.1111/jcpe.13921
摘要

Abstract Aim We sought to investigate the release of neutrophil extracellular traps (NETs) in neutrophils from individuals with rheumatoid arthritis (RA) and controls and compare the presence of NETs in gingival tissues according to periodontal status. Also, the association between single nucleotide polymorphisms (SNPs) of the peptidyl arginine deaminase type 4 ( PADI4 ) gene and the GTG haplotype with RA, periodontitis and NETs was evaluated in vitro. Materials and Methods Peripheral neutrophils were isolated by density gradient, and NET concentration was determined by the PicoGreen method. Immunofluorescence was studied to identify NETs by co‐localization of myeloperoxidase (MPO)‐citrullinated histone H3 (H3Cit). Genotyping for SNPs ( PADI4 _89; PADI4 _90; PADI4 _92; and PADI4 _104) was performed in 87 individuals with RA and 111 controls. Results The release of NETs in vitro was significantly higher in individuals with RA and periodontitis and when stimulated with Porphyromonas gingivalis . Gingival tissues from subjects with RA and periodontitis revealed increased numbers of MPO‐H3Cit‐positive cells. Individuals with the GTG haplotype showed a higher release of NETs in vitro and worse periodontal parameters. Conclusions The release of NETs by circulating neutrophils is associated with RA and periodontitis and is influenced by the presence of the GTG haplotype.
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