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亚精胺激活线粒体三功能蛋白并改善小鼠的抗肿瘤免疫。

Spermidine activates mitochondrial trifunctional protein and improves antitumor immunity in mice.

机构信息

Division of Immunology and Genomic Medicine, Center for Cancer Immunotherapy and Immunobiology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

National Genetic Center, Ministry of Health, Muscat, Oman.

出版信息

Science. 2022 Oct 28;378(6618):eabj3510. doi: 10.1126/science.abj3510.

Abstract

Spermidine (SPD) delays age-related pathologies in various organisms. SPD supplementation overcame the impaired immunotherapy against tumors in aged mice by increasing mitochondrial function and activating CD8 T cells. Treatment of naïve CD8 T cells with SPD acutely enhanced fatty acid oxidation. SPD conjugated to beads bound to the mitochondrial trifunctional protein (MTP). In the MTP complex, synthesized and purified from , SPD bound to the α and β subunits of MTP with strong affinity and allosterically enhanced their enzymatic activities. T cell-specific deletion of the MTP α subunit abolished enhancement of programmed cell death protein 1 (PD-1) blockade immunotherapy by SPD, indicating that MTP is required for SPD-dependent T cell activation.

摘要

亚精胺(SPD)可延缓多种生物体与年龄相关的病变。SPD 补充剂通过增加线粒体功能和激活 CD8 T 细胞,克服了老年小鼠中受损的肿瘤免疫治疗。SPD 处理幼稚 CD8 T 细胞可急性增强脂肪酸氧化。SPD 与珠结合物与线粒体三功能蛋白(MTP)结合。在 MTP 复合物中,从 中合成和纯化,SPD 与 MTP 的α和β亚基具有很强的亲和力结合,并变构增强它们的酶活性。MTP α 亚基的 T 细胞特异性缺失消除了 SPD 对程序性细胞死亡蛋白 1(PD-1)阻断免疫治疗的增强作用,表明 MTP 是 SPD 依赖的 T 细胞激活所必需的。

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