Lai Junzhong, Luo Xuan, Tian Shuoran, Zhang Xing, Huang Shanlu, Wang Hanze, Li Qiumei, Cai Shaoli, Chen Qi
Fujian Key Laboratory of Innate Immune Biology, Biomedical Research Center of South China, Fujian Normal University Qishan Campus, Fuzhou, China.
College of Life Science, Fujian Normal University Qishan Campus, Fuzhou, China.
Front Pharmacol. 2020 Feb 28;11:88. doi: 10.3389/fphar.2020.00088. eCollection 2020.
Cyclic GMP-AMP (cGAMP) synthase (cGAS) is a major DNA sensor responsible for cytosolic DNA-mediated innate immune response. Inhibition of cGAS may be an effective strategy for treating autoimmune diseases such as Aicardi-Goutieres syndrome and systemic lupus erythematosus. Compound C (also known as Dorsomorphin) has been annotated as a potent and reversible inhibitor for AMPKs as well as ALK protein kinases. Here, we report a new function of Compound C which can suppress dsDNA-dependent type I interferon induction. These effects were not dependent on the activities of AMPK proteins. o assays and liquid chromatograph-mass spectrometry data show that Compound C has the capability of reducing cGAMP accumulation, suggesting that Compound C may function as a modulator involved in the cGAS-STING-mediated DNA sensing pathway. Furthermore, Compound C is able to rescue the autoimmune phenotypes in a mouse model carrying the Trex1 gene deficiency. These data demonstrate a new and inverse correlation between Compound C and type I interferon production in response to dsDNA signaling.
环磷酸鸟苷-腺苷酸(cGAMP)合酶(cGAS)是负责胞质DNA介导的先天性免疫反应的主要DNA传感器。抑制cGAS可能是治疗诸如Aicardi-Goutieres综合征和系统性红斑狼疮等自身免疫性疾病的有效策略。化合物C(也称为 Dorsomorphin)已被标注为AMPK以及ALK蛋白激酶的强效可逆抑制剂。在此,我们报道了化合物C的一种新功能,即它可以抑制双链DNA依赖性I型干扰素的诱导。这些效应不依赖于AMPK蛋白的活性。实验分析和液相色谱-质谱数据表明,化合物C具有减少cGAMP积累的能力,这表明化合物C可能作为一种调节剂参与cGAS-STING介导的DNA传感途径。此外,化合物C能够挽救携带Trex1基因缺陷的小鼠模型中的自身免疫表型。这些数据证明了化合物C与响应双链DNA信号的I型干扰素产生之间存在新的负相关关系。