SESN1 negatively regulates STING1 to maintain innate immune homeostasis.

Autophagy Pub Date : 2025-06-01 Epub Date: 2025-02-13 DOI:10.1080/15548627.2025.2463148
Lingxiao Xu, Hongqian Zhang, Zuocheng Qiu, Shijing Wang, Chaoyang Wang, Hao Cheng, Qianya Wan, Mingyu Pan
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Abstract

STING1 is a central hub protein of CGAS-STING1 signaling which is important signaling axis to sense DNA for the host against pathogens infection through regulating type I interferon (IFN-I) production. However, excessive STING1 activation-induced overproduced IFN-I triggers tissue damage and autoimmune disorders. Thus, the activity of STING1 must be precisely regulated for immune homeostasis. Here, we discovered SESN1 (sestrin 1) as an essential negative regulator of STING1 to maintain immune homeostasis. Upon herpes simplex virus-1 (HSV-1) infection, the expression of SESN1 was downregulated, which enhanced potentiality to virus defense for host. Consistently, SESN1-deficient mice exhibited stronger ability against HSV-1 infection compared to wild-type littermates. Additionally, we found the expression of SESN1 was decreased in systemic lupus erythematosus (SLE) patients and trex1 KO mouse model of autoimmune disease. Intriguingly, the replenishment of SESN1 effectively impressed IFN-I production and autoimmune responses in the PBMCs of human SLE specimens and the trex1 KO mouse model both in vitro and in vivo. Mechanistically, SESN1 targeted STING1 and promoted STING1 autophagic degradation by facilitating the interaction of SQSTM1/p62 and STING1. Together, our study uncovers a crucial role of SESN1 for immune homeostasis to balance anti-virus and autoimmunity by regulating STING1. SESN1 might be a potential therapeutic target for infectious and autoimmune diseases.Abbreviations: BMDMs: bone marrow-derived macrophages; cGAMP: cyclic GMP-AMP; CGAS: cyclic GMP-AMP synthase; HTDNA: herring testes DNA; IFNA4: interferon alpha 4; IFNB: interferon beta; IRF3: interferon regulatory factor 3; ISD: interferon stimulatory DNA; ISGs: IFN-stimulated genes; PBMCs: peripheral blood mononuclear cells; RSAD2: radical S-adenosyl methionine domain containing 2; SLE: systemic lupus erythematosus; STING1: stimulator of interferon response cGAMP interactor 1; TBK1: TANK binding kinase 1.

SESN1负向调控STING1以维持先天免疫稳态。
STING1是CGAS-STING1信号的中心枢纽蛋白,是通过调节I型干扰素(IFN-I)的产生,为宿主抵抗病原体感染感知DNA的重要信号轴。然而,过度的STING1激活诱导过度产生IFN-I会引发组织损伤和自身免疫性疾病。因此,必须精确调节STING1的活性以维持免疫稳态。在这里,我们发现SESN1 (sestrin 1)是STING1维持免疫稳态的重要负调控因子。单纯疱疹病毒1 (HSV-1)感染后,SESN1表达下调,增强了宿主对病毒的防御能力。与野生型小鼠相比,sesn1缺陷小鼠表现出更强的抗HSV-1感染能力。此外,我们发现SESN1在系统性红斑狼疮(SLE)患者和自身免疫性疾病trex1 KO小鼠模型中的表达降低。有趣的是,在体外和体内,SESN1的补充有效地影响了人SLE标本和trex1 KO小鼠模型的pbmc中IFN-I的产生和自身免疫反应。机制上,SESN1通过促进SQSTM1/p62与STING1的相互作用,靶向STING1并促进其自噬降解。总之,我们的研究揭示了SESN1在免疫稳态中的关键作用,通过调节STING1来平衡抗病毒和自身免疫。SESN1可能是感染性和自身免疫性疾病的潜在治疗靶点。bmmdms:骨髓源性巨噬细胞;cGAMP:环GMP-AMP;CGAS:环GMP-AMP合成酶;HTDNA:鲱鱼睾丸DNA;IFNA4:干扰素α 4;IFNB:干扰素;IRF3:干扰素调节因子3;ISD:干扰素刺激DNA;ISGs: ifn刺激基因;外周血单个核细胞;RSAD2:含2的s -腺苷基蛋氨酸结构域;SLE:系统性红斑狼疮;STING1:干扰素应答刺激因子cGAMP相互作用因子1;TBK1: TANK结合激酶1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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