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α-生育酚对两栖类和人类杯状细胞的颗粒物粘膜炎性具有保护作用。

Alpha-tocopherol exerts protective function against the mucotoxicity of particulate matter in amphibian and human goblet cells.

机构信息

Biological and Genetic Resources Assessment Division, National Institute of Biological Resources, Incheon, 22689, Korea.

School of Life Sciences, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, South Korea.

出版信息

Sci Rep. 2020 Apr 10;10(1):6224. doi: 10.1038/s41598-020-63085-6.

Abstract

Exposure to particulate matter (PM) in ambient air is known to increase the risk of cardiovascular disorders and mortality. The cytotoxicity of PM is mainly due to the abnormal increase of reactive oxygen species (ROS), which damage cellular components such as DNA, RNA, and proteins. The correlation between PM exposure and human disorders, including mortality, is based on long-term exposure. In this study we have investigated acute responses of mucus-secreting goblet cells upon exposure to PM derived from a heavy diesel engine. To this end, we employed the mucociliary epithelium of amphibian embryos and human Calu-3 cells to examine PM mucotoxicity. Our data suggest that acute exposure to PM significantly impairs mucus secretion and results in the accumulation of mucus vesicles in the cytoplasm of goblet cells. RNA-seq analysis revealed that acute responses to PM exposure significantly altered gene expression patterns; however, known regulators of mucus production and the secretory pathway were not significantly altered. Interestingly, pretreatment with α-tocopherol nearly recovered the hyposecretion of mucus from both amphibian and human goblet cells. We believe this study demonstrates the mucotoxicity of PM and the protective function of α-tocopherol on mucotoxicity caused by acute PM exposure from heavy diesel engines.

摘要

暴露于环境空气中的颗粒物(PM)已知会增加心血管疾病和死亡率的风险。PM 的细胞毒性主要是由于活性氧(ROS)的异常增加,ROS 会破坏 DNA、RNA 和蛋白质等细胞成分。PM 暴露与包括死亡率在内的人类疾病之间的相关性是基于长期暴露的。在这项研究中,我们研究了暴露于源自重型柴油发动机的 PM 后分泌粘液的杯状细胞的急性反应。为此,我们采用了两栖动物胚胎和人 Calu-3 细胞的纤毛上皮来检查 PM 对粘液的毒性。我们的数据表明,急性 PM 暴露会显著损害粘液分泌,并导致杯状细胞细胞质中粘液小泡的积累。RNA-seq 分析显示,急性 PM 暴露会显著改变基因表达模式;然而,已知的粘液产生和分泌途径的调节剂并没有明显改变。有趣的是,α-生育酚预处理几乎可以恢复两栖动物和人杯状细胞中粘液的低分泌。我们相信,这项研究证明了 PM 的粘液毒性,以及α-生育酚对急性 PM 暴露引起的粘液毒性的保护作用,这种 PM 来自重型柴油发动机。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f232/7148342/2fad83a1e66f/41598_2020_63085_Fig1_HTML.jpg

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