Laboratory of Immune Response Dynamics, WPI Immunology Frontier Research Center, Osaka University, Suita, Osaka, Japan.
Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Sci Immunol. 2023 Mar 31;8(81):eadc9324. doi: 10.1126/sciimmunol.adc9324.
Celastrol, a bioactive molecule extracted from the plant, has been shown to exhibit anti-inflammatory properties. However, its mechanism of action has not been fully elucidated. Here, we show that celastrol suppresses humoral immune responses and autoimmunity by disabling a protein complex consisting of copper metabolism MURR1 domain-containing (COMMD) 3 and COMMD8 (COMMD3/8 complex), a signaling adaptor for chemoattractant receptors. Having demonstrated the involvement of the COMMD3/8 complex in a mouse model of rheumatoid arthritis, we identified celastrol as a compound that covalently bound to and dissociated the COMMD3/8 complex. Celastrol inhibited B cell migration, reduced antibody responses, and blocked arthritis progression, recapitulating deficiency of the COMMD3/8 complex. These effects of celastrol were abolished in mice expressing a celastrol-resistant mutant of the COMMD3/8 complex. These findings establish that celastrol exerts immunosuppressive activity by targeting the COMMD3/8 complex. Our study suggests that the COMMD3/8 complex is a potentially druggable target in autoimmune diseases and points to celastrol as a lead pharmacologic candidate in this capacity.
从植物中提取的生物活性分子雷公藤红素具有抗炎特性。然而,其作用机制尚未完全阐明。在这里,我们表明雷公藤红素通过使包含铜代谢 MURR1 结构域的 COMMD3 和 COMMD8(COMMD3/8 复合物)的蛋白质复合物失活来抑制体液免疫反应和自身免疫。由于已经证明 COMMD3/8 复合物参与了类风湿关节炎的小鼠模型,我们鉴定出雷公藤红素是一种与 COMMD3/8 复合物结合并使其解聚的化合物。雷公藤红素抑制 B 细胞迁移,减少抗体反应,并阻断关节炎进展,重现 COMMD3/8 复合物的缺陷。在表达雷公藤红素抗性 COMMD3/8 复合物突变体的小鼠中,雷公藤红素的这些作用被消除。这些发现表明雷公藤红素通过靶向 COMMD3/8 复合物发挥免疫抑制活性。我们的研究表明,COMMD3/8 复合物是自身免疫性疾病中一个潜在的可成药靶点,并指出雷公藤红素是具有这种作用的潜在药物候选物。