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热休克反应调节因子 HSF1 调控 NK 细胞的抗肿瘤免疫

英文原题:The stress response regulator HSF1 modulates natural killer cell anti-tumour immunity.

查看英文原题

The stress response regulator HSF1 modulates natural killer cell anti-tumour immunity.

PubMed 2024/09/02(内容时间) Nat Cell Biol Q1 · IF 22.7(JCR 2025)

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中文摘要

多种细胞损伤均汇聚于热休克因子1(HSF1)的激活,HSF1调控蛋白质毒性应激反应以维持蛋白质稳态。HSF1以细胞类型和情境特异性的方式调控蛋白质毒性应激反应之外的众多基因程序,从而促进恶性肿瘤。然而,HSF1在肿瘤微环境免疫群体中的作用仍不明确。在此,我们利用HSF1激活的体内模型和单细胞转录组肿瘤分析,证明自然杀伤(NK)细胞中HSF1活性增强会损害细胞毒性、细胞因子产生及随后的抗肿瘤免疫。在机制上,HSF1直接结合并调控NK细胞效应功能关键介质的表达。这项工作表明,HSF1在肿瘤微环境的应激条件下调控免疫反应。这些发现对于提高过继性NK细胞疗法的疗效以及设计包括NK细胞介导肿瘤杀伤调节剂在内的联合策略具有重要意义。

展开英文摘要原文

Diverse cellular insults converge on activation of the heat shock factor 1 (HSF1), which regulates the proteotoxic stress response to maintain protein homoeostasis. HSF1 regulates numerous gene programmes beyond the proteotoxic stress response in a cell-type- and context-specific manner to promote malignancy.

However, the role(s) of HSF1 in immune populations of the tumour microenvironment remain elusive.

Here, we leverage an in vivo model of HSF1 activation and single-cell transcriptomic tumour profiling to show that augmented HSF1 activity in natural killer (NK) cells impairs cytotoxicity, cytokine production and subsequent anti-tumour immunity.

Mechanistically, HSF1 directly binds and regulates the expression of key mediators of NK cell effector function. This work demonstrates that HSF1 regulates the immune response under the stress conditions of the tumour microenvironment.

These findings have important implications for enhancing the efficacy of adoptive NK cell therapies and for designing combinatorial strategies including modulators of NK cell-mediated tumour killing.

论文信息

作者
Hockemeyer K、Sakellaropoulos T、Chen X、Ivashkiv O、Sirenko M、Zhou H、Gambi G、Battistello E
第一作者单位
Department of Pathology, NYU Grossman School of Medicine, New York, NY, USA.United States
通讯作者单位
Department of Pathology, NYU Grossman School of Medicine, New York, NY, USA. Ioannis.Aifantis@nyulangone.org.United States
期刊
Nature cell biology2024 Oct
原文标识
PubMed 39223375 · DOI 10.1038/s41556-024-01490-z