Induction of LY6E regulates interleukin-1β production, potentially contributing to the immunopathogenesis of systemic lupus erythematosus.

IF 8.2 2区 生物学 Q1 CELL BIOLOGY Cell Communication and Signaling Pub Date : 2025-03-20 DOI:10.1186/s12964-025-02140-z
Jenn-Haung Lai, De-Wei Wu, Chuan-Yueh Huang, Li-Feng Hung, Chien-Hsiang Wu, Shuk-Man Ka, Ann Chen, Jing-Long Huang, Ling-Jun Ho
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Abstract

Systemic lupus erythematosus (SLE) is an autoimmune disorder characterized by the deposition of immune complexes (ICs) in various organs, especially the kidney, leading to lupus nephritis, one of the major and therapeutically challenging manifestations of SLE. Among the various cytokines induced in SLE, type I interferons (IFN-Is) play crucial roles in mediating immunopathogenesis, and anti-IFN-I treatment has been approved for SLE treatment. The uptake of ICs by macrophages results in macrophage activation, which initiates, triggers, and exaggerates immune responses in SLE. After observing the induction of an IFN-stimulated gene, LY6E, in monocytes from SLE patients, we demonstrated the colocalization of both LY6E and a macrophage marker in kidneys from pristane-induced lupus-prone mice and from patients with lupus nephritis. By studying mouse bone marrow-derived macrophages, we showed that LY6E regulated IFN-α- and IC-induced production and secretion of mature interleukin-1β (mIL-1β), foam cell formation and several mitochondria-associated mechanisms, such as the release of mitochondrial DNA (mtDNA) but not mitochondrial RNA (mtRNA) into the cytosol, the generation of mitochondrial reactive oxygen species (mtROS) and ROS, the activation of caspase 1, NLRP3, and the stimulator of interferon genes (STING) signaling pathway, and the activation of cytidine/uridine monophosphate kinase 2 (CMPK2), which were involved in LY6E-mediated immunomodulatory effects. In addition, synergistic effects of a combination of IL-1β and IFN-α and of IL-1β and ICs on the induction of the expression of IFN-stimulated genes were observed. In addition to revealing the proinflammatory roles and mechanisms of LY6E in macrophages, given that various subgroups of macrophages have been identified in the kidneys of patients with lupus nephritis, targeted treatment aimed at LY6E may be a potential therapeutic for lupus nephritis.

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诱导LY6E调节白细胞介素-1β的产生,可能有助于系统性红斑狼疮的免疫发病机制。
系统性红斑狼疮(SLE)是一种自身免疫性疾病,其特征是免疫复合物(ic)在各器官,特别是肾脏沉积,导致狼疮肾炎,狼疮肾炎是SLE的主要和治疗挑战性表现之一。在SLE诱导的各种细胞因子中,I型干扰素(IFN-Is)在介导免疫发病机制中起着至关重要的作用,抗ifn -I治疗已被批准用于SLE治疗。巨噬细胞对ic的摄取导致巨噬细胞活化,从而启动、触发和夸大SLE的免疫反应。在观察了ifn刺激的基因LY6E在SLE患者单核细胞中的诱导作用后,我们证实了LY6E和巨噬细胞标记物在普利斯坦诱导的狼疮易感小鼠和狼疮肾炎患者肾脏中的共定位。通过对小鼠骨髓源性巨噬细胞的研究,我们发现LY6E调节IFN-α和ic诱导的成熟白细胞介素-1β (mIL-1β)的产生和分泌,泡沫细胞的形成和一些线粒体相关机制,如线粒体DNA (mtDNA)的释放而不是线粒体RNA (mtRNA)进入细胞质,线粒体活性氧(mtROS)和ROS的产生,caspase 1, NLRP3,干扰素基因(STING)信号通路的刺激因子,胞苷/尿苷单磷酸激酶2 (CMPK2)的激活,参与ly6e介导的免疫调节作用。此外,我们还观察了IL-1β与IFN-α以及IL-1β与ic联合诱导IFN刺激基因表达的协同效应。除了揭示LY6E在巨噬细胞中的促炎作用和机制外,鉴于在狼疮性肾炎患者的肾脏中已经发现了各种巨噬细胞亚群,针对LY6E的靶向治疗可能是狼疮性肾炎的潜在治疗方法。
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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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