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Cytotoxicity analysis of ambient fine particle in BEAS-2B cells on an air-liquid interface (ALI) microfluidics system

机译:气液界面(ALI)微流控系统对BEAS-2B细胞中环境微粒的细胞毒性分析

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摘要

Ambient fine particle is a crucial indicator of air pollution brought into the air by sundry natural and public events. However, a comprehensive understanding of the PM2.5-induced cytotoxicity especially the contribution of bioaerosol part is still undiscovered. Herein, an ALI microfluidics system integrated multi-omits (iTRAQ & RNA-seq) was successfully utilized to recognize the molecular mechanisms induced by microorganisms carried bioaerosol in human lung epithelial cells. The cells viability was above 98% within 21 days on this system. Moreover, the results showed that eight microorganisms-related pathways (e.g., Salmonella. amoebiasis, HMV-I) were activated after exposure to PM2.5 for 24 h, which played a certain proportion in contributing to inflammation reaction. In addition, multi-omits demonstrated that three inflammation-related signal transduction cascades including MAPK signaling pathway. TNF signaling pathway, and TGF signaling pathway were triggered by fine particles, ultimately leading to apoptosis-related process disorder by associated cytokines like TNF, IL6, and TGF-beta. Furthermore, flow cytometry analysis showed that the cell apoptosis rate increased from 3.8% to 66.7% between the cells exposed to PM2.5 (10 mu g/cm(2)) for 24 h and untreated control cells, which indicated that the fine particles had the ability to activate apoptosis-related signal cascades and result in apoptosis. ELISA assay and western blot indicated that HO-1, JNK, IL6, TNF, NF-kappa B. and FGF14 were significantly increased after exposure to PM2.5 while Casp3 and FGFR were decreased, which were consistent with the multi-omits. Moreover, PM2.5 components (OC, EC, 16PAHs, As, Cu, Mn, Cl-, and NO3-) were significantly correlated to the inflammation related proteins and cytokines, which played a vital role in the inflammation and apoptosis related signaling pathways. These findings pointed to strong links among microorganisms infection, inflammation, and apoptosis in cell response to PM2.5 carried microorganisms. It also provided a new approach for understanding PM2.5 induced cytotoxicity and health risks. (C) 2019 Elsevier B.V. All rights reserved.
机译:环境细颗粒物是各种自然和公共事件带入空气中的空气污染的重要指标。但是,尚未发现对PM2.5诱导的细胞毒性,特别是生物气溶胶部分的贡献的全面了解。在本文中,成功地利用集成了多种遗漏的ALI微流控系统(iTRAQ和RNA-seq)来识别人肺上皮细胞中携带生物气溶胶的微生物诱导的分子机制。在该系统上,细胞存活率在21天内超过98%。此外,结果表明,暴露于PM2.5 24小时后,激活了八个与微生物相关的途径(例如沙门氏菌,阿米巴病,HMV-1),这在炎症反应中起了一定的作用。此外,多次缺失显示了三个与炎症相关的信号转导级联反应,包括MAPK信号通路。 TNF信号通路和TGF信号通路被细颗粒触发,最终通过相关的细胞因子如TNF,IL6和TGF-β导致凋亡相关的过程紊乱。此外,流式细胞仪分析显示,暴露于PM2.5(10μg / cm(2))24小时的细胞与未经处理的对照细胞之间的细胞凋亡率从3.8%增加到66.7%,这表明细颗粒具有激活凋亡相关信号级联并导致凋亡的能力。 ELISA法和Western blot检测结果表明,暴露于PM2.5后HO-1,JNK,IL6,TNF,NF-κB和FGF14显着升高,而Casp3和FGFR降低,这与多突变体一致。此外,PM2.5成分(OC,EC,16PAH,As,Cu,Mn,Cl-和NO3-)与炎症相关的蛋白质和细胞因子显着相关,在炎症和凋亡相关的信号通路中起着至关重要的作用。 。这些发现指出了微生物感染,炎症和细胞对PM2.5携带的微生物的反应中的凋亡之间的紧密联系。它还为了解PM2.5诱导的细胞毒性和健康风险提供了一种新方法。 (C)2019 Elsevier B.V.保留所有权利。

著录项

  • 来源
    《The Science of the Total Environment》 |2019年第10期|108-119|共12页
  • 作者单位

    Fudan Univ, Shanghai Key Lab Atmospher Particle Pollut Preven, Dept Environm Sci & Engn, 220 Handan Rd, Shanghai 200433, Peoples R China;

    Fudan Univ, Shanghai Key Lab Atmospher Particle Pollut Preven, Dept Environm Sci & Engn, 220 Handan Rd, Shanghai 200433, Peoples R China|Univ Shanghai Sci & Technol, Engn Res Ctr Opt Instrument & Syst, Minist Educ, Shanghai Key Lab Modern Opt Syst, 516 Jungong Rd, Shanghai 200093, Peoples R China;

    Fudan Univ, Shanghai Key Lab Atmospher Particle Pollut Preven, Dept Environm Sci & Engn, 220 Handan Rd, Shanghai 200433, Peoples R China;

    Fudan Univ, Shanghai Key Lab Atmospher Particle Pollut Preven, Dept Environm Sci & Engn, 220 Handan Rd, Shanghai 200433, Peoples R China;

    Fudan Univ, Shanghai Key Lab Atmospher Particle Pollut Preven, Dept Environm Sci & Engn, 220 Handan Rd, Shanghai 200433, Peoples R China;

    Fudan Univ, Shanghai Key Lab Atmospher Particle Pollut Preven, Dept Environm Sci & Engn, 220 Handan Rd, Shanghai 200433, Peoples R China;

    Fudan Univ, Shanghai Key Lab Atmospher Particle Pollut Preven, Dept Environm Sci & Engn, 220 Handan Rd, Shanghai 200433, Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    PM2.5; ALI microfluidics system; Multi-omics (iTRAQ combined RNA-seq); Microorganisms; Inflammation; Apoptosis;

    机译:PM2.5;ALI微流控系统;多组学(iTRAQ组合RNA-seq);微生物;炎症;凋亡;

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