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慢性暴露于聚苯乙烯纳米塑料会导致小鼠肠道机械和免疫屏障功能障碍。

Chronic exposure to polystyrene nanoplastics induces intestinal mechanical and immune barrier dysfunction in mice.

机构信息

School of Basic Medical Sciences, Binzhou Medical University, Yantai 264003, China.

School of Basic Medical Sciences, Binzhou Medical University, Yantai 264003, China.

出版信息

Ecotoxicol Environ Saf. 2024 Jan 1;269:115749. doi: 10.1016/j.ecoenv.2023.115749. Epub 2023 Nov 30.

Abstract

Micro(nano)plastics are prevalent in the environment, and prolonged exposure to them represents a threat to human health. The goal of this study is to assess the health risk of long-term exposure to nanoplastics (NPs) at environmental concentrations on the intestinal mechanical and immune barrier in mice. In this study, mice were provided drinking water containing polystyrene NPs (PS-NPs; 0.1, 1, and 10 mg·L) for 32 consecutive weeks. The levels of endocytosis proteins caveolin and clathrin and of tight junctional proteins claudin-1, occludin, and ZO-1, and morphological changes, proportion of lymphocytes B in MLNs and lymphocytes T in IELs and LPLs were determined by immunohistochemistry, hematoxylin-eosin, and flow cytometry assays in the intestinal tissues of mice at 28 weeks. The activities or concentrations of ROS, SOD, MDA, and GSH-Px and inflammatory factors (IL-1β, IL-6, and TNF-α) in the intestinal tissues of mice were measured by ELISA at 12, 16, 20, 24, and 32 weeks. Compared with the control group, oral ingested PS-NPs entered the intestinal tissues of mice and upregulated expression levels of the clathrin and caveolin. The intestinal tissue structure of mice in the PS-NPs (1 and 10 mg·L) exposure groups showed significant abnormalities, such as villus erosion, decreased of crypts numbers and large infiltration of inflammatory cells. Exposure to 0.1 mg·L PS-NPs decreased occludin protein levels, but not claudin-1 and ZO-1 levels. The levels of these three tight junction proteins decreased significantly in the 1 and 10 mg·L PS-NPs exposed groups. Exposure to PS-NPs led to a significant time- and dose-dependent increase in ROS and MDA levels, and concurrently decreased GSH-Px and SOD contents. Exposure to PS-NPs increased the proportion of B cells in MLNs, and decreased the proportion of CD8 T cells in IELs and LPLs. The levels of pro-inflammatory cytokines IL-6, TNF-α and IL-1β were markedly elevated after PS-NPs exposure. Long-term PS-NPs exposure impaired intestinal mechanical and immune barrier, and indicate a potentially significant threat to human health.

摘要

微(纳)塑料在环境中普遍存在,长期暴露于其中对人类健康构成威胁。本研究旨在评估环境浓度下长期暴露于纳米塑料(NPs)对小鼠肠道机械和免疫屏障的健康风险。在这项研究中,小鼠连续 32 周饮用含有聚苯乙烯 NPs(PS-NPs;0.1、1 和 10mg·L)的水。通过免疫组织化学、苏木精-伊红和流式细胞术检测 28 周时小鼠肠道组织中内吞蛋白小窝蛋白和网格蛋白、紧密连接蛋白 Claudin-1、Occludin 和 ZO-1 的水平,以及形态变化、肠系膜淋巴结中 B 淋巴细胞和上皮内淋巴细胞和固有层淋巴细胞中 T 淋巴细胞的比例。在 12、16、20、24 和 32 周时,通过 ELISA 测量小鼠肠道组织中 ROS、SOD、MDA 和 GSH-Px 及炎症因子(IL-1β、IL-6 和 TNF-α)的活性或浓度。与对照组相比,口服摄入的 PS-NPs 进入小鼠肠道组织,上调网格蛋白和小窝蛋白的表达水平。PS-NPs(1 和 10mg·L)暴露组小鼠肠道组织结构出现明显异常,如绒毛侵蚀、隐窝数量减少和大量炎症细胞浸润。0.1mg·L PS-NPs 暴露组降低了 Occludin 蛋白水平,但 Claudin-1 和 ZO-1 水平没有降低。在 1 和 10mg·L PS-NPs 暴露组,这三种紧密连接蛋白的水平显著降低。PS-NPs 暴露导致 ROS 和 MDA 水平显著增加,而 GSH-Px 和 SOD 含量降低,呈时间和剂量依赖性。PS-NPs 暴露增加了肠系膜淋巴结中 B 细胞的比例,降低了上皮内淋巴细胞和固有层淋巴细胞中 CD8 T 细胞的比例。PS-NPs 暴露后促炎细胞因子 IL-6、TNF-α 和 IL-1β 的水平显著升高。长期 PS-NPs 暴露会损害肠道机械和免疫屏障,对人类健康构成潜在威胁。

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