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单细胞RNA测序揭示了全氟辛酸对小鼠肠道微环境的重塑作用。

Single cell RNA sequencing reveals the reshaping effect of perfluorooctanoic acid on the intestinal microenvironment of mice.

作者信息

Gao Ya, Guan Jiayun, Zhou Rui, Li Zewei, Chen Tianyang, Yang Kaican, Huang Rong, Huang Yue, Zheng Siting, Huang Zhenhua, Rong Xiaoxiang

机构信息

Department of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

Department of Oncology, Ganzhou People's Hospital, Ganzhou 341000, China.

出版信息

Ecotoxicol Environ Saf. 2025 Sep 1;302:118540. doi: 10.1016/j.ecoenv.2025.118540. Epub 2025 Jun 25.

Abstract

Perfluorooctanoic acid (PFOA), a prevalent perfluorinated compound pollutants, has been implicated in the development of various gastrointestinal disorders. However, the specific PFOA-induced intestinal microenvironment alterations remain poorly characterized. In this study, we established a chronic PFOA toxicity model in C57BL/6 mice of both sexes through exposure to PFOA at doses of 0, 1, 5, and 10 mg/kg/day. Single-cell RNA sequencing (scRNA-seq) was performed on the small intestine tissues from female mice, and key findings were validated through flow cytometry and immunohistochemistry. Histopathological analysis revealed that PFOA induced intestinal damage in both sexes, with a more severe impact observed in female mice. scRNA-seq analysis demonstrated that PFOA treatment triggered abnormal proliferation of intestinal epithelial cells, particularly the expansion of Ada enterocyte cells, suggesting their potential role in injury repair process. Furthermore, PFOA exposure induced significant remodeling of the intestinal immune microenvironment, characterized by decreased overall lymphocyte infiltration, heightened activation of remaining cytotoxic CD8 T cells, and a notable increase in proliferative CD8 T cells. A significant reduction in FOXP3 regulatory T cells further contributed to a pro-inflammatory shift within the T cell population. Cell-cell interaction analysis revealed enhanced macrophage-CD8 T cell communication via the CCR1-CCL5 axis, suggesting a synergistic role in driving inflammatory responses. This study presents a comprehensive analysis of PFOA-induced intestinal microenvironment remodeling at single-cell resolution, providing novel insights into the pathophysiological mechanisms underlying PFOA-associated intestinal diseases. SYNOPSIS: Minimal research exists on PFOA-induced intestinal microenvironment changes. The study shows that abnormal hyperplasia and dysfunction of intestinal epithelial cell, along with immuno microenvironment dysregulation, create an inflammatory environment, potentially linked to PFOA-induced systemic toxicity.

摘要

全氟辛酸(PFOA)是一种普遍存在的全氟化合物污染物,与多种胃肠道疾病的发生有关。然而,PFOA诱导的肠道微环境改变的具体情况仍不清楚。在本研究中,我们通过以0、1、5和10mg/kg/天的剂量给C57BL/6雌雄小鼠暴露PFOA,建立了慢性PFOA毒性模型。对雌性小鼠的小肠组织进行了单细胞RNA测序(scRNA-seq),并通过流式细胞术和免疫组织化学验证了关键发现。组织病理学分析表明,PFOA对雌雄小鼠均诱导了肠道损伤,雌性小鼠受到的影响更严重。scRNA-seq分析表明,PFOA处理引发了肠道上皮细胞的异常增殖,特别是Ada肠细胞的扩增,表明它们在损伤修复过程中可能发挥作用。此外,PFOA暴露诱导了肠道免疫微环境的显著重塑,其特征是总体淋巴细胞浸润减少、剩余细胞毒性CD8 T细胞的激活增强以及增殖性CD8 T细胞显著增加。FOXP3调节性T细胞的显著减少进一步导致了T细胞群体内的促炎转变。细胞间相互作用分析显示,巨噬细胞与CD8 T细胞通过CCR1-CCL5轴的通信增强,表明在驱动炎症反应中起协同作用。本研究在单细胞分辨率下对PFOA诱导的肠道微环境重塑进行了全面分析,为PFOA相关肠道疾病的病理生理机制提供了新的见解。摘要:关于PFOA诱导的肠道微环境变化的研究很少。该研究表明,肠道上皮细胞的异常增生和功能障碍,以及免疫微环境失调,会产生炎症环境,这可能与PFOA诱导的全身毒性有关。

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