通过抑制 M1 巨噬细胞中的 HMGB1/TLR4/STAT3 轴,抑制铁凋亡可拯救 M2 巨噬细胞并缓解关节炎

IF 10.7 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Redox Biology Pub Date : 2024-06-24 DOI:10.1016/j.redox.2024.103255
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引用次数: 0

摘要

铁变态反应是由铁依赖性脂质过氧化驱动的一种程序性细胞死亡。TNF 介导的谷胱甘肽生物合成已被证明能保护增生滑膜中的滑膜成纤维细胞免受铁氧化。通过减少滑膜成纤维细胞的数量,诱导铁变态反应为类风湿性关节炎(RA)提供了一种新的治疗方法。类风湿性关节炎滑膜炎的开始和维持在很大程度上受到巨噬细胞的影响,因为它们产生的细胞因子会促进炎症并导致软骨和骨骼的破坏。然而,巨噬细胞在红斑狼疮中易受铁蛋白沉积影响的程度仍不清楚。在这项研究中,我们发现在关节炎滑膜的高含铁量环境中,M2 巨噬细胞比 M1 巨噬细胞更容易发生铁蛋白沉积,导致 M1/M2 比例失调。在铁跃迁过程中,M2 巨噬细胞释放的 HMGB1 与 M1 巨噬细胞上的 TLR4 相互作用,进而引发 M1 巨噬细胞中 STAT3 信号的激活,导致炎症反应。敲除 TLR4 可降低 M1 巨噬细胞中由 HMGB1 诱导的细胞因子水平。在胶原抗体诱导的关节炎(CIA)模型小鼠无症状阶段开始使用铁蛋白沉积抑制剂脂氧司他丁-1(Lip-1),而在胶原抗体诱导的关节炎(CAIA)发病初期在M2巨噬细胞中过表达GPX4可保护M2巨噬细胞免于铁蛋白沉积细胞死亡,并显著阻止关节炎症和破坏的发展。因此,我们的研究证明了在增生性滑膜的微环境中,M2巨噬细胞易受铁凋亡的影响,并揭示了HMGB1/TLR4/STAT3轴对铁凋亡的M2巨噬细胞加剧RA滑膜炎症的能力至关重要。我们的研究结果为了解 RA 的进展和治疗提供了新的视角。
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Inhibition of ferroptosis rescues M2 macrophages and alleviates arthritis by suppressing the HMGB1/TLR4/STAT3 axis in M1 macrophages

Ferroptosis is a type of programmed cell death driven by iron-dependent lipid peroxidation. The TNF-mediated biosynthesis of glutathione has been shown to protect synovial fibroblasts from ferroptosis in the hyperplastic synovium. Ferroptosis induction provides a novel therapeutic approach for rheumatoid arthritis (RA) by reducing the population of synovial fibroblasts. The beginning and maintenance of synovitis in RA are significantly influenced by macrophages, as they generate cytokines that promote inflammation and contribute to the destruction of cartilage and bone. However, the vulnerability of macrophages to ferroptosis in RA remains unclear. In this study, we found that M2 macrophages are more vulnerable to ferroptosis than M1 macrophages in the environment of the arthritis synovium with a high level of iron, leading to an imbalance in the M1/M2 ratio. During ferroptosis, HMGB1 released by M2 macrophages interacts with TLR4 on M1 macrophages, which in turn triggers the activation of STAT3 signaling in M1 macrophages and contributes to the inflammatory response. Knockdown of TLR4 decreased the level of cytokines induced by HMGB1 in M1 macrophages. The ferroptosis inhibitor liproxstatin-1 (Lip-1) started at the presymptomatic stage in collagen-induced arthritis (CIA) model mice, and GPX4 overexpression in M2 macrophages at the onset of collagen antibody-induced arthritis (CAIA) protected M2 macrophages from ferroptotic cell death and significantly prevented the development of joint inflammation and destruction. Thus, our study demonstrated that M2 macrophages are vulnerable to ferroptosis in the microenvironment of the hyperplastic synovium and revealed that the HMGB1/TLR4/STAT3 axis is critical for the ability of ferroptotic M2 macrophages to contribute to the exacerbation of synovial inflammation in RA. Our findings provide novel insight into the progression and treatment of RA.

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来源期刊
Redox Biology
Redox Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
19.90
自引率
3.50%
发文量
318
审稿时长
25 days
期刊介绍: Redox Biology is the official journal of the Society for Redox Biology and Medicine and the Society for Free Radical Research-Europe. It is also affiliated with the International Society for Free Radical Research (SFRRI). This journal serves as a platform for publishing pioneering research, innovative methods, and comprehensive review articles in the field of redox biology, encompassing both health and disease. Redox Biology welcomes various forms of contributions, including research articles (short or full communications), methods, mini-reviews, and commentaries. Through its diverse range of published content, Redox Biology aims to foster advancements and insights in the understanding of redox biology and its implications.
期刊最新文献
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