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在人体肺细胞中暴露于生物量燃烧气溶胶成分(左旋葡聚糖和 4-硝基儿茶酚)下的细胞毒性和线粒体功能障碍的证据。

Evidence for cytotoxicity and mitochondrial dysfunction in human lung cells exposed to biomass burning aerosol constituents: Levoglucosan and 4-nitrocatechol.

机构信息

Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224, Warsaw, Poland.

Cytomics Core Facility, Príncipe Felipe Research Center, Avda. Eduardo Primo Yúfera, 3, 46012, Valenica, Spain.

出版信息

Environ Pollut. 2024 Dec 15;363(Pt 2):125173. doi: 10.1016/j.envpol.2024.125173. Epub 2024 Oct 21.

Abstract

Biomass burning (BB) emissions are one of the largest sources of carbonaceous aerosol, posing a significant risk as an airway irritant. Important BB markers include wood pyrolysis emissions, such as levoglucosan (LG) that is an anhydrous sugar bearing a six-carbon ring structure (i.e., 1,6-anhydro-β-D-glucopyranose). Atmospheric chemical aging of BB-derived aerosol (BBA) in the presence of nitrogen oxides (NO) can yield nitro-aromatic compounds, including 4-nitrocatechol (4NC). There is building evidence that NO-mediated chemical aging of BBA poses a more serious exposure effect than primary pyrolysis emissions. This study provides a comparative toxicological assessment following the exposure to important BBA marker compounds in human lung cells (i.e., A549 and BEAS-2B) to determine whether aromatic 4NC is more toxic than BBA-bound anhydrous carbohydrate (i.e., LG). We determined inhibitory concentration-50 (IC) and examined reactive oxygen species (ROS) changes, mitochondrial dysfunction, and apoptosis induction in the two cell lines following exposure to LG and 4NC in a dose-response manner. In the BEAS-2B cells, estimated IC values for 4NC were 33 and 8.8 μg mL, and for LG were 2546 and ∼3 × 10 μg mL at 24 h and 48 h of exposure, respectively. A549 cells exhibited a much higher IC value than BEAS-2B cells. LG exposures resulted in mitochondrial stress with viability inhibition, but cells recovered with increasing exposure time. 4NC exposures at 200 μg mL resulted in the induction of apoptosis at 6 h. Mitochondrial dysfunction and ROS imbalance induced the intrinsic apoptotic pathway induction following 4NC exposures. While increased ROS is caused by LG exposure in lung cells, 4NC is a marker of concern during BB emissions, as we observed apoptosis and high mitochondrial ROS in both lung cells at atmospherically-relevant aerosol concentrations. It may be associated with higher airway or inhalation pathologies in higher BBA emissions, such as wildfires or during wood combustion.

摘要

生物质燃烧(BB)排放是碳质气溶胶的最大来源之一,作为一种气道刺激物,构成了重大风险。重要的 BB 标志物包括木质热解排放物,如左旋葡聚糖(LG),它是一种无水糖,带有六碳环结构(即 1,6-脱水-β-D-吡喃葡萄糖)。在存在氮氧化物(NO)的情况下,BB 衍生气溶胶(BBA)的大气化学老化可以产生硝基芳香族化合物,包括 4-硝基邻苯二酚(4NC)。越来越多的证据表明,与初级热解排放物相比,BBA 的 NO 介导的化学老化构成了更严重的暴露效应。本研究在人类肺细胞(即 A549 和 BEAS-2B)中暴露于重要的 BBA 标志物化合物后提供了一种比较毒理学评估,以确定芳香族 4NC 是否比 BBA 结合的无水碳水化合物(即 LG)更具毒性。我们以剂量反应的方式确定了 A549 和 BEAS-2B 细胞中 LG 和 4NC 暴露后抑制浓度-50(IC)和活性氧物种(ROS)变化、线粒体功能障碍和细胞凋亡诱导。在 BEAS-2B 细胞中,4NC 的估计 IC 值分别为 33 和 8.8μg/mL,LG 的 IC 值分别为 2546 和 3×10μg/mL,暴露时间分别为 24 和 48 小时。A549 细胞的 IC 值明显高于 BEAS-2B 细胞。LG 暴露导致线粒体应激,细胞活力受到抑制,但随着暴露时间的增加细胞恢复。4NC 暴露在 200μg/mL 时,在 6 小时时导致细胞凋亡。线粒体功能障碍和 ROS 失衡诱导 4NC 暴露后的内在凋亡途径诱导。虽然在肺细胞中 LG 暴露会导致 ROS 增加,但 4NC 是 BB 排放期间需要关注的标志物,因为我们在大气相关气溶胶浓度下观察到两种肺细胞的细胞凋亡和高水平的线粒体 ROS。它可能与更高的气道或吸入性疾病有关,例如野火或木材燃烧时的 BBA 排放较高。

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