Gpx4 通过防止脂质过氧化和铁氧化调节不变 NKT 细胞的稳态和功能

IF 3.6 3区 医学 Q2 IMMUNOLOGY
Sophia P M Sok, Kaitlyn Pipkin, Narcis I Popescu, Megan Reidy, Bin Li, Holly Van Remmen, Mike Kinter, Xiao-Hong Sun, Zhichao Fan, Meng Zhao
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引用次数: 0

摘要

不变NKT(iNKT)细胞是一类先天性类T细胞,在免疫稳态和激活中发挥着重要作用。我们发现,与 CD4+ T 细胞相比,iNKT 细胞在小鼠和人类体内的脂质过氧化水平明显更高。蛋白质组分析还表明,iNKT 细胞表达较高水平的磷脂氢过氧化物酶谷胱甘肽过氧化物酶 4 (Gpx4),这是一种主要的抗氧化酶,可减少脂质过氧化并防止铁变态反应。T 细胞特异性缺失 Gpx4 会减少 iNKT 细胞数量,其中最突出的是产生 IFN-γ 的 NKT1 亚群。RNA序列分析表明,iNKT细胞中的IFN-γ信号传导、细胞周期调控和线粒体功能都受到了Gpx4缺失的干扰。同样,我们在 Gpx4 基因敲除的 iNKT 细胞中检测到细胞因子生成受损、细胞增殖和细胞死亡增加、脂质过氧化物和线粒体活性氧积累。铁跃迁抑制剂、铁螯合剂、维生素 E 和维生素 K2 可防止 iNKT 细胞因 Gpx4 缺乏而诱导铁跃迁,并改善 iNKT 细胞因 Gpx4 抑制而受损的功能。最后,维生素 E 能拯救 Gpx4 基因敲除小鼠的 iNKT 细胞群。总之,我们的研究结果揭示了 Gpx4 通过控制脂质过氧化和铁变态反应在调节 iNKT 细胞稳态和功能方面的关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gpx4 Regulates Invariant NKT Cell Homeostasis and Function by Preventing Lipid Peroxidation and Ferroptosis.

Invariant NKT (iNKT) cells are a group of innate-like T cells that plays important roles in immune homeostasis and activation. We found that iNKT cells, compared with CD4+ T cells, have significantly higher levels of lipid peroxidation in both mice and humans. Proteomic analysis also demonstrated that iNKT cells express higher levels of phospholipid hydroperoxidase glutathione peroxidase 4 (Gpx4), a major antioxidant enzyme that reduces lipid peroxidation and prevents ferroptosis. T cell-specific deletion of Gpx4 reduces iNKT cell population, most prominently the IFN-γ-producing NKT1 subset. RNA-sequencing analysis revealed that IFN-γ signaling, cell cycle regulation, and mitochondrial function are perturbed by Gpx4 deletion in iNKT cells. Consistently, we detected impaired cytokine production, elevated cell proliferation and cell death, and accumulation of lipid peroxides and mitochondrial reactive oxygen species in Gpx4 knockout iNKT cells. Ferroptosis inhibitors, iron chelators, vitamin E, and vitamin K2 can prevent ferroptosis induced by Gpx4 deficiency in iNKT cells and ameliorate the impaired function of iNKT cells due to Gpx4 inhibition. Last, vitamin E rescues iNKT cell population in Gpx4 knockout mice. Altogether, our findings reveal the critical role of Gpx4 in regulating iNKT cell homeostasis and function, through controlling lipid peroxidation and ferroptosis.

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来源期刊
Journal of immunology
Journal of immunology 医学-免疫学
CiteScore
8.20
自引率
2.30%
发文量
495
审稿时长
1 months
期刊介绍: The JI publishes novel, peer-reviewed findings in all areas of experimental immunology, including innate and adaptive immunity, inflammation, host defense, clinical immunology, autoimmunity and more. Special sections include Cutting Edge articles, Brief Reviews and Pillars of Immunology. The JI is published by The American Association of Immunologists (AAI)
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