Otsuka Yasuo, Masuta Yasuhiro, Minaga Kosuke, Okai Natsuki, Hara Akane, Takada Ryutaro, Masaki Sho, Kamata Ken, Honjo Hajime, Yamashita Kouhei, Kudo Masatoshi, Watanabe Tomohiro
Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka 589-8511, Japan.
Department of Hematology and Oncology, Kyoto University Graduate School of Medicine, 54 Shogoin-kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan.
J Clin Biochem Nutr. 2024 Jul;75(1):46-53. doi: 10.3164/jcbn.23-77. Epub 2023 Dec 19.
Neutrophils express protein arginine deiminase 2 and PAD4, both of which mediate the citrullination of target proteins to induce production of neutrophil extracellular traps. Although PAD-dependent NETs trigger inflammatory bowel disease, the mechanisms governing the expression of PAD2 and PAD4 are poorly understood. In this study, we tried to clarify expression mechanisms of PAD2 and PAD4 in the colonic mucosa of patients with ulcerative colitis and Crohn's disease. Administration of Cl-amidine, a pan PAD-inhibitor, attenuated the development of dextran sodium sulfate-induced colitis, the effects of which were accompanied by reduced IL-6 and TNF-α production by colonic lamina propria mononuclear cells upon exposure to Toll-like receptor ligands. The mRNA expression of colonic and was negatively and positively correlated with disease activity and pro-inflammatory cytokine responses in patients with UC, respectively. Reciprocal regulation of and mRNA expression was observed in the colonic mucosa of UC patients, but not in those of CD patients. mRNA expression was correlated with disease activity and pro-inflammatory cytokine responses in patients with CD. Collectively, these data suggest that reciprocal regulation of PAD2 and PAD4 expression is associated with disease activity in UC patients.
中性粒细胞表达蛋白精氨酸脱亚氨酶2(PAD2)和PAD4,二者均可介导靶蛋白的瓜氨酸化以诱导中性粒细胞胞外陷阱的产生。尽管依赖PAD的中性粒细胞胞外陷阱会引发炎症性肠病,但PAD2和PAD4的表达调控机制仍知之甚少。在本研究中,我们试图阐明溃疡性结肠炎和克罗恩病患者结肠黏膜中PAD2和PAD4的表达机制。给予泛PAD抑制剂氯苯脒可减轻葡聚糖硫酸钠诱导的结肠炎的发展,其作用伴随着结肠固有层单核细胞在暴露于Toll样受体配体时IL-6和TNF-α产生的减少。UC患者结肠中PAD2和PAD4的mRNA表达分别与疾病活动度和促炎细胞因子反应呈负相关和正相关。在UC患者的结肠黏膜中观察到PAD2和PAD4 mRNA表达的相互调节,但在CD患者中未观察到。PAD4 mRNA表达与CD患者的疾病活动度和促炎细胞因子反应相关。总体而言,这些数据表明PAD2和PAD4表达的相互调节与UC患者的疾病活动度相关。