University of MT, Center for Environmental Health Sciences, Missoula, MT, USA.
Department of Biomedical Sciences, University of MN Medical School, Duluth, MN, USA.
Inhal Toxicol. 2024 Jul;36(6):367-377. doi: 10.1080/08958378.2024.2354398. Epub 2024 May 20.
Due to climate change, wildfires have increased in intensity and duration. While wildfires threaten lives directly, the smoke has more far-reaching adverse health impacts. During an extreme 2017 wildfire event, residents of Seeley Lake, Montana were exposed to unusually high levels of wood smoke (WS) causing sustained effects on lung function (decreased FEV/FVC). The present study utilized an animal model of WS exposure to research cellular and molecular mechanisms of the resulting health effects. Mice were exposed to inhaled WS utilizing locally harvested wood to recapitulate community exposures. WS was generated at a rate resulting in a 5 mg/m PM exposure for five days. This exposure resulted in a similar 0.28 mg/m particle deposition (lung surface area) in mice that was calculated for human exposure. As with the community observations, there was a significant effect on lung function, increased resistance, and decreased compliance, that was more pronounced in males at an extended (2 months) timepoint and males were more affected than females: assays illustrated changes to alveolar macrophage functions (increased TNFα secretion and decreased efferocytosis). Female mice had significantly elevated IL-33 levels in lungs, however, pretreatment of male mice with IL-33 resulted in an abrogation of the observed WS effects, suggesting a dose-dependent role of IL-33. Additionally, there were greater immunotoxic effects in male mice. These findings replicated the outcomes in humans and suggest that IL-33 is involved in a mechanism of the adverse effects of WS exposures that inform on potential sex differences.
由于气候变化,野火的强度和持续时间都有所增加。虽然野火直接威胁生命,但烟雾对健康的影响更为深远。在 2017 年一场极端的野火事件中,蒙大拿州 Seeley Lake 的居民暴露在异常高浓度的木烟(WS)中,导致肺功能持续下降(FEV/FVC 降低)。本研究利用 WS 暴露的动物模型,研究导致健康影响的细胞和分子机制。研究人员使用当地采集的木材使小鼠吸入 WS,以重现社区暴露情况。WS 的产生速度使小鼠每天暴露于 5mg/m 的 PM 中,持续 5 天。这种暴露导致小鼠肺部的颗粒沉积量(肺表面积)与人类暴露时的 0.28mg/m 相似。与社区观察结果一样,该暴露对肺功能有显著影响,增加了阻力,降低了顺应性,在延长(2 个月)时间点时,雄性的影响更为明显,而且雄性比雌性更易受影响:实验表明肺泡巨噬细胞功能发生变化(TNFα 分泌增加,吞噬作用减少)。然而,雄性小鼠预先用 IL-33 处理后,其肺部的 IL-33 水平显著升高,但观察到的 WS 影响被消除,这表明 IL-33 具有剂量依赖性。此外,雄性小鼠的免疫毒性作用更大。这些发现与人类的结果一致,表明 IL-33 参与了 WS 暴露不良影响的机制,这为潜在的性别差异提供了依据。