1-C代谢中的SARDH塑造了t细胞的命运,并作为潜在的癌症治疗靶点。

IF 19.8 1区 医学 Q1 IMMUNOLOGY
Wen Si, Sijin Cheng, Haiyin He, Yu Zhang, Yuhui Miao, Dingcheng Yi, Mengjiao Ni, Anqiang Wang, Hongtao Fan, Yufei Bo, Chang Liu, Zhaode Bu, Linnan Zhu, Zemin Zhang
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引用次数: 0

摘要

t细胞代谢在确定t细胞功能状态中起着关键作用。通过对全面的胰腺癌单细胞转录图谱的分析,我们确定了SARDH,一种参与一碳(1-C)代谢的酶,作为潜在的t细胞代谢检查点。SARDH显著影响t细胞命运和功能,导致肿瘤控制效果受损。敲除SARDH导致肌氨酸积累和s -腺苷蛋氨酸(SAM)的消耗减少,SAM是表观遗传调节的关键甲基供体,可能是由于甘氨酸到肌氨酸稳态的转变。SARDH的缺失增加了NF-κB激活基因的H3K79me2修饰,从而增强了NF-κB信号传导和t细胞功能。此外,我们观察到各种癌症类型的肿瘤中1-C代谢的转录失调,这通常伴随着肌氨酸水平的增加。研究发现,肌氨酸可诱导SARDH上调,提示肿瘤内T细胞代谢稳态存在反馈机制。这些发现强调了靶向1-C代谢,特别是SARDH作为癌症治疗途径的潜在作用和机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SARDH in the 1-C metabolism sculpts the T-cell fate and serves as a potential cancer therapeutic target.

T-cell metabolism plays a pivotal role in defining T-cell functional states. Through analysis of a comprehensive pancancer single-cell transcriptional atlas, we identified SARDH, an enzyme involved in one-carbon (1-C) metabolism, as a potential T-cell metabolic checkpoint. SARDH significantly impacts T-cell fate and function, leading to impaired tumor control efficacy. Knocking down SARDH resulted in sarcosine accumulation and reduced consumption of S-adenosylmethionine (SAM), a critical methyl donor for epigenetic modulation, likely due to the shift in glycine-to-sarcosine homeostasis. Deletion of SARDH increased H3K79me2 modification at NF-κB-activating genes, thereby augmenting NF-κB signaling and T-cell function. Additionally, we observed transcriptional dysregulation of 1-C metabolism within tumors across various cancer types, which was often accompanied by increased sarcosine levels. Sarcosine was found to induce SARDH upregulation, suggesting a feedback mechanism for metabolic homeostasis in T cells within tumors. These findings underscore the potential effects and mechanism of targeting 1-C metabolism, particularly SARDH, as an avenue for cancer therapy.

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来源期刊
CiteScore
31.20
自引率
1.20%
发文量
903
审稿时长
1 months
期刊介绍: Cellular & Molecular Immunology, a monthly journal from the Chinese Society of Immunology and the University of Science and Technology of China, serves as a comprehensive platform covering both basic immunology research and clinical applications. The journal publishes a variety of article types, including Articles, Review Articles, Mini Reviews, and Short Communications, focusing on diverse aspects of cellular and molecular immunology.
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