Takenaka Shin-Ichi, Kaieda Shinjiro, Kawayama Tomotaka, Matsuoka Masanobu, Kaku Yoichiro, Kinoshita Takashi, Sakazaki Yuki, Okamoto Masaki, Tominaga Masaki, Kanesaki Katsuya, Chiba Asako, Miyake Sachiko, Ida Hiroaki, Hoshino Tomoaki
Department of Medicine, Division of Respirology, Neurology and Rheumatology, Kurume University School of Medicine, Kurume 830-0011, Japan.
Nagata Orthopedic Hospital, Omuta 836-0843, Japan.
Biochem Biophys Rep. 2015 Oct 31;4:386-391. doi: 10.1016/j.bbrep.2015.10.015. eCollection 2015 Dec.
The newly characterized cytokine IL-38 (IL-1F10) belongs to the IL-1 family of cytokines. Previous work has demonstrated that IL-38 inhibited -induced IL-17 production from peripheral blood mononuclear cells. However, it is still unclear whether IL-38 is an inflammatory or an anti-inflammatory cytokine. We generated anti-human IL-38 monoclonal antibodies in order to perform immunohistochemical staining and an enzyme-linked immunosorbent assay. While human recombinant IL-38 protein was not cleaved by recombinant caspase-1, chymase, or PR3 in vitro, overexpression of IL-38 cDNA produced a soluble form of IL-38 protein. Furthermore, immunohistochemical analysis showed that synovial tissues obtained from RA patients strongly expressed IL-38 protein. To investigate the biological role of IL-38, C57BL/6 IL-38 gene-deficient () mice were used in an autoantibody-induced rheumatoid arthritis (RA) mouse model. As compared with control mice, IL-38 mice showed greater disease severity, accompanied by higher IL-1β and IL-6 gene expression in the joints. Therefore, IL-38 acts as an inhibitor of the pathogenesis of autoantibody-induced arthritis in mice and may have a role in the development or progression of RA in humans.
新鉴定的细胞因子白细胞介素-38(IL-38,即IL-1F10)属于白细胞介素-1细胞因子家族。先前的研究表明,IL-38可抑制外周血单核细胞诱导产生白细胞介素-17。然而,IL-38究竟是促炎细胞因子还是抗炎细胞因子仍不清楚。我们制备了抗人IL-38单克隆抗体,以便进行免疫组织化学染色和酶联免疫吸附测定。虽然人重组IL-38蛋白在体外未被重组半胱天冬酶-1、糜酶或蛋白酶3切割,但IL-38 cDNA的过表达产生了一种可溶性形式的IL-38蛋白。此外,免疫组织化学分析显示,类风湿关节炎(RA)患者的滑膜组织中IL-38蛋白表达强烈。为了研究IL-38的生物学作用,我们在自身抗体诱导的类风湿关节炎(RA)小鼠模型中使用了C57BL/6 IL-38基因缺陷()小鼠。与对照小鼠相比,IL-38基因缺陷小鼠的疾病严重程度更高,同时关节中白细胞介素-1β和白细胞介素-6的基因表达也更高。因此,IL-38在小鼠自身抗体诱导的关节炎发病机制中起抑制作用,可能在人类RA的发生或发展中发挥作用。