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Peptidylarginine deiminase type 4 deficiency reduced arthritis severity in a glucose-6-phosphate isomerase-induced arthritis model

机译:在6磷酸葡萄糖异构酶诱导的关节炎模型中肽酰精氨酸脱亚氨酶4型缺乏症降低了关节炎的严重程度

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摘要

Peptidyl arginine deiminase 4 (PAD4) is an enzyme that is involved in protein citrullination, and is a target for anti-citrullinated peptide antibodies (ACPAs) in rheumatoid arthritis (RA). Genetic polymorphisms in the PADI4 gene encoding PAD4 are associated with RA susceptibility. We herein analyzed the roles of PADI4 in inflammatory arthritis using a glucose-6-phosphate isomerase (GPI)-induced arthritis (GIA) model in Padi4 knockout (KO) mice. Arthritis severity, serum anti-GPI antibody titers, and IL-6 concentrations were significantly reduced in Padi4 KO mice. The frequency of Th17 cells was decreased in GPI-immunized Padi4 KO mice, whereas WT and Padi4-deficient naïve CD4+ T cells displayed the same efficiencies for Th17 cell differentiation in vitro. In addition, the numbers of myeloid lineage cells were reduced with the increased expression of pro-apoptotic genes in GPI-immunized Padi4 KO mice. Furthermore, the survival of Padi4-deficient neutrophils was impaired in vitro. Our results suggest that PADI4 exacerbates arthritis with diverse immunological modifications.
机译:肽基精氨酸脱亚氨酶4(PAD4)是一种参与蛋白质瓜氨酸化的酶,是类风湿关节炎(RA)中抗瓜氨酸化肽抗体(ACPA)的靶标。编码PAD4的PADI4基因中的遗传多态性与RA易感性有关。我们在本文中使用Padi4基因敲除(KO)小鼠中的葡萄糖-6磷酸异构酶(GPI)诱导的关节炎(GIA)模型分析了PADI4在炎性关节炎中的作用。 Padi4 KO小鼠的关节炎严重程度,血清抗GPI抗体滴度和IL-6浓度均显着降低。在GPI免疫的Padi4 KO小鼠中,Th17细胞的频率降低,而野生型和Padi4缺失的CD4 + T细胞在Th17细胞体外分化中显示出相同的效率。另外,随着GPI免疫的Padi4 KO小鼠中促凋亡基因表达的增加,髓系谱系细胞的数量减少。此外,缺乏Padi4的中性粒细胞的存活在体外受到损害。我们的结果表明,PADI4具有多种免疫学修饰,可加重关节炎。

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