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聚苯乙烯微/纳米塑料通过肠道微生物群、代谢物和细胞因子的串扰诱导造血损伤。

Polystyrene micro-/nanoplastics induced hematopoietic damages via the crosstalk of gut microbiota, metabolites, and cytokines.

机构信息

Department of Epidemiology and Health Statistics, School of Public Health, Capital Medical University, Beijing 10069, PR China.

Department of Occupational Health and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, PR China.

出版信息

Environ Int. 2022 Mar;161:107131. doi: 10.1016/j.envint.2022.107131. Epub 2022 Feb 8.

Abstract

Micro-/nanoplastics (MNPLs), novel environmental pollutants, widely exist in the environment and life and bring health risks. Previous studies have shown that NMPLs can penetrate bone marrow, but whether they cause hematopoietic damage remains uncertain. In this study, C57BL/6J mice were treated with polystyrene MNPLs (PS-MNPLs, 10 μm, 5 μm and 80 nm) at 60 μg doses for 42 days by intragastric administration. We evaluated the hematopoietic toxicity induced by MNPLs and potential mechanisms via combining 16S rRNA, metabolomics, and cytokine chips. The results demonstrated that PS-MNPLs induced hematopoietic toxicity, which was manifested by the disorder of bone marrow cell arrangement, the reduction in colony-forming, self-renewal and differentiation capacity, and the increased proportion of lymphocytes. PS-MNPLs also disrupted the homeostasis of the gut microbiota, metabolism, and inflammation, all of which were correlated with hematotoxicity, suggesting that abnormal gut microbiota-metabolite-cytokine axes might be the crucial pathways in MNPLs-induced hematopoietic injury. In conclusion, our study systematically demonstrated that multi-scale PS-MNPLs induced hematopoietic toxicity via the crosstalk of gut microbiota, metabolites, and cytokines and provided valuable insights into MNPLs toxicity, which was conducive to health risk assessment and informed policy decisions regarding PS-MNPLs.

摘要

微/纳米塑料(MNPLs)是一种新型环境污染物,广泛存在于环境和生活中,带来健康风险。先前的研究表明,NMPLs 可以穿透骨髓,但它们是否会造成造血损伤仍不确定。在这项研究中,通过灌胃给予 C57BL/6J 小鼠 60μg 剂量的聚苯乙烯 MNPLs(PS-MNPLs,10μm、5μm 和 80nm),共 42 天,以评估 MNPLs 引起的造血毒性及其潜在机制,方法是结合 16S rRNA、代谢组学和细胞因子芯片。结果表明,PS-MNPLs 诱导造血毒性,表现为骨髓细胞排列紊乱、集落形成、自我更新和分化能力降低以及淋巴细胞比例增加。PS-MNPLs 还破坏了肠道微生物群、代谢和炎症的内稳态,所有这些都与造血毒性相关,表明异常的肠道微生物群-代谢物-细胞因子轴可能是 MNPLs 诱导造血损伤的关键途径。总之,本研究系统地表明,多尺度 PS-MNPLs 通过肠道微生物群、代谢物和细胞因子的相互作用诱导造血毒性,并为 MNPLs 毒性提供了有价值的见解,有利于健康风险评估和 PS-MNPLs 的政策决策。

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