肠道微生物代谢物丁酸盐通过cxcl11依赖性增强自然杀伤细胞浸润来抑制肝癌的生长。

IF 12.2 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Gut Microbes Pub Date : 2025-12-01 Epub Date: 2025-06-27 DOI:10.1080/19490976.2025.2519706
Menghan Zhang, Xuefeng Huang, Yanlong Zhang, Minghang Yu, Xiaoxue Yuan, Yifan Xu, Lei Ma, Xi Wang, Huichun Xing
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引用次数: 0

摘要

肠道微生物来源的丁酸盐在小鼠肝细胞癌(HCC)模型中起着至关重要的作用。然而,丁酸盐发挥其作用的精确分子机制在很大程度上是不明确的。采用气相色谱-质谱联用(GC-MS)定量测定血浆短链脂肪酸(SCFAs),以了解其与HCC预后的关系。流式细胞术检测肿瘤浸润性免疫细胞。使用体外实验研究了丁酸盐和自然杀伤(NK)细胞之间的相互作用,包括迁移、细胞毒性脱粒和共培养实验。通过中和实验进行体内验证。通过RNA测序(RNA-seq)、染色质免疫沉淀测序(ChIP-seq)和转座酶可及染色质测序(ATAC-seq)进一步研究丁酸盐调控的分子通路。肝细胞癌患者血浆丁酸盐水平升高与预后改善呈正相关。值得注意的是,丁酸盐通过增强NK细胞向肿瘤组织的浸润来抑制肿瘤进展。机制上,丁酸盐刺激细胞因子分泌,显著增强趋化因子CXCL11的产生,从而促进NK细胞浸润。基因集富集分析(GSEA)显示,丁酸盐刺激后,肝肿瘤细胞系的趋化因子信号通路和NK细胞介导的细胞毒性通路上调。此外,转录组学和表观基因组学分析表明,暴露于丁酸盐诱导了由STAT家族转录因子调控的染色质可及性和增强子重塑。我们的研究表明,丁酸盐能够增强CXCL11的表达。这可能是由于染色质重塑,进而促进NK细胞浸润,对HCC发挥有效的抗肿瘤作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut microbial metabolite butyrate suppresses hepatocellular carcinoma growth via CXCL11-dependent enhancement of natural killer cell infiltration.

Gut microbiota-derived butyrate plays a vital role in attenuating hepatocellular carcinoma (HCC) in murine models. However, the precise molecular mechanisms by which butyrate exerts its effects are largely undefined. Plasma short-chain fatty acids (SCFAs) were quantitatively measured by using gas chromatography-mass spectrometry (GC-MS) to access their association with HCC prognosis. Tumor-infiltrating immune cells were characterized by flow cytometry. The interactions between butyrate and natural killer (NK) cells were studied using in vitro assays, including migration, cytotoxic degranulation, and co-culture experiments. In vivo validation was conducted through neutralization experiments. The molecular pathways regulated by butyrate were further investigated by employing RNA sequencing (RNA-seq), chromatin immunoprecipitation sequencing (ChIP-seq), and Assay for Transposase-Accessible Chromatin using sequencing (ATAC-seq). A positive correlation was observed between elevated plasma butyrate levels and improved prognosis in HCC patients. Notably, butyrate inhibited tumor progression by enhancing NK cell infiltration into tumor tissues. Mechanistically, butyrate stimulated cytokine secretion, notably significantly enhancing the production of the chemokine CXCL11, thereby facilitating NK cell infiltration. Gene Set Enrichment Analysis (GSEA) of hepatic tumor cell lines revealed that the chemokine signaling and NK cell-mediated cytotoxicity pathways were upregulated following butyrate stimulation. Furthermore, transcriptomic and epigenomic analyses showed that exposure to butyrate induced de novo chromatin accessibility and enhancer remodeling, regulated by STAT family transcription factors. Our study demonstrated that butyrate was able to enhance the expression of CXCL11. This is likely attributed to chromatin remodeling, and then promoting NK cell infiltration and exerting effective anti-tumor effects on HCC.

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来源期刊
Gut Microbes
Gut Microbes Medicine-Microbiology (medical)
CiteScore
18.20
自引率
3.30%
发文量
196
审稿时长
10 weeks
期刊介绍: The intestinal microbiota plays a crucial role in human physiology, influencing various aspects of health and disease such as nutrition, obesity, brain function, allergic responses, immunity, inflammatory bowel disease, irritable bowel syndrome, cancer development, cardiac disease, liver disease, and more. Gut Microbes serves as a platform for showcasing and discussing state-of-the-art research related to the microorganisms present in the intestine. The journal emphasizes mechanistic and cause-and-effect studies. Additionally, it has a counterpart, Gut Microbes Reports, which places a greater focus on emerging topics and comparative and incremental studies.
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