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Gpx4 通过防止脂质过氧化和铁死亡来调节不变自然杀伤 T 细胞的稳态和功能。

Gpx4 Regulates Invariant NKT Cell Homeostasis and Function by Preventing Lipid Peroxidation and Ferroptosis.

机构信息

Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK.

Department of Cellular and Molecular Medicine, School of Medicine, University of California-San Diego, La Jolla, CA.

出版信息

J Immunol. 2024 Oct 1;213(7):941-951. doi: 10.4049/jimmunol.2400246.

Abstract

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.

摘要

不变自然杀伤 T(iNKT)细胞是一群先天样 T 细胞,在免疫稳态和激活中发挥重要作用。我们发现,与 CD4+T 细胞相比,iNKT 细胞在小鼠和人类中均具有更高水平的脂质过氧化。蛋白质组学分析还表明,iNKT 细胞表达更高水平的磷脂氢过氧化物谷胱甘肽过氧化物酶 4(Gpx4),这是一种主要的抗氧化酶,可降低脂质过氧化并防止铁死亡。T 细胞特异性敲除 Gpx4 会减少 iNKT 细胞群,尤其是产生 IFN-γ 的 NKT1 亚群。RNA 测序分析显示,IFN-γ 信号、细胞周期调控和线粒体功能在 iNKT 细胞中受到 Gpx4 缺失的干扰。一致地,我们检测到细胞因子产生受损、增殖和细胞死亡增加,以及 Gpx4 敲除 iNKT 细胞中脂质过氧化物和线粒体活性氧的积累。铁死亡抑制剂、铁螯合剂、维生素 E 和维生素 K2 可预防 Gpx4 缺乏诱导的 iNKT 细胞铁死亡,并改善 Gpx4 抑制导致的 iNKT 细胞功能障碍。最后,维生素 E 可挽救 Gpx4 敲除小鼠中的 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死亡在调节 iNKT 细胞稳态和功能中的关键作用。

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