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藜芦碱通过靶向 COMMD3/8 复合物抑制体液免疫反应和自身免疫。

Celastrol suppresses humoral immune responses and autoimmunity by targeting the COMMD3/8 complex.

机构信息

Laboratory of Immune Response Dynamics, WPI Immunology Frontier Research Center, Osaka University, Suita, Osaka, Japan.

Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.

出版信息

Sci Immunol. 2023 Mar 31;8(81):eadc9324. doi: 10.1126/sciimmunol.adc9324.

Abstract

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.

摘要

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。

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