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聚六亚甲基胍消毒剂致肺纤维化的肺表面活性物质生物合成阻滞。

Pulmonary surfactant biogenesis blockage mediated polyhexamethylene guanidine disinfectant induced pulmonary fibrosis.

机构信息

Clinical Medical Research Center for Women and Children Diseases, Shandong Provincial Maternal and Child Health Care Hospital Affiliated to Qingdao University, Jinan 250001, China; Department of Environmental and Occupational Health, School of Public Health, Qingdao University, Qingdao 266071, China; CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology of China, Beijing 100190, China.

Department of Environmental and Occupational Health, School of Public Health, Qingdao University, Qingdao 266071, China.

出版信息

J Hazard Mater. 2024 Dec 5;480:136307. doi: 10.1016/j.jhazmat.2024.136307. Epub 2024 Oct 28.

Abstract

The widespread use of disinfectants and inhalation exposure to aerosolized forms is closely associated with adverse health effects on the respiratory system and pulmonary fibrosis, but the mechanism remains unclear. Here, we investigated the time-course pulmonary fibrosis effects of polyhexamethylene guanidine (PHMG) disinfectant inhalation exposure and elucidated its underlying mechanism. Specifically, scRNA-seq analysis revealed an initial increase in epithelial cell numbers after 4 weeks of PHMG exposure during induced pulmonary fibrosis, followed by a subsequent decrease after 8 weeks of exposure. Mechanistically, PHMG disrupted autophagic flux leading to intracellular accumulation and blocked pulmonary surfactant biogenesis in alveolar type II epithelial (AT2) cells both in vitro and in vivo. Furthermore, intervention studies using metformin confirmed that autophagy dysfunction mediated the blockage of pulmonary surfactant biogenesis in AT2 cells, playing a pivotal role in PHMG-induced pulmonary fibrosis. Our elucidation of these toxicological mechanisms provides valuable insights into the pathogenesis of pulmonary fibrosis triggered by environmental PHMG exposure, thereby offering a promising therapeutic target for mitigating and treating PHMG-associated pulmonary fibrosis.

摘要

聚六亚甲基胍(PHMG)消毒剂吸入暴露与呼吸系统不良健康影响和肺纤维化密切相关,但机制尚不清楚。在这里,我们研究了聚六亚甲基胍消毒剂吸入暴露的时间进程性肺纤维化效应,并阐明了其潜在机制。具体来说,单细胞 RNA 测序分析显示,在诱导性肺纤维化 4 周后,PHMG 暴露会导致上皮细胞数量最初增加,8 周后则会减少。在机制上,PHMG 破坏了自噬流,导致细胞内堆积,并在体外和体内阻断肺泡 II 型上皮(AT2)细胞中肺表面活性物质的生物发生。此外,使用二甲双胍的干预研究证实,自噬功能障碍介导了 AT2 细胞中肺表面活性物质生物发生的阻断,在 PHMG 诱导的肺纤维化中发挥关键作用。我们对这些毒理学机制的阐明为环境 PHMG 暴露引发的肺纤维化发病机制提供了有价值的见解,从而为减轻和治疗 PHMG 相关肺纤维化提供了有希望的治疗靶点。

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