Biosciences and Biotechnology Division, Physical and Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, CA 94550, USA.
Public Health and Integrated Toxicology Division, Center for Public Health and Environmental Assessment, U.S. Environmental Protection Agency, Research Triangle Park, NC 27709, USA.
Int J Mol Sci. 2024 Sep 24;25(19):10288. doi: 10.3390/ijms251910288.
The frequency, duration, and size of wildfires have been increasing, and the inhalation of wildfire smoke particles poses a significant risk to human health. Epidemiological studies have shown that wildfire smoke exposure is positively associated with cognitive and neurological dysfunctions. However, there is a significant gap in knowledge on how wildfire smoke exposure can affect the blood-brain barrier and cause molecular and cellular changes in the brain. Our study aims to determine the acute effect of smoldering eucalyptus wood smoke extract (WSE) on brain endothelial cells for potential neurotoxicity in vitro. Primary human brain microvascular endothelial cells (HBMEC) and immortalized human brain endothelial cell line (hCMEC/D3) were treated with different doses of WSE for 24 h. WSE treatment resulted in a dose-dependent increase in IL-8 in both HBMEC and hCMEC/D3. RNA-seq analyses showed a dose-dependent upregulation of genes involved in aryl hydrocarbon receptor (AhR) and nuclear factor erythroid 2-related factor 2 (NRF2) pathways and a decrease in tight junction markers in both HBMEC and hCMEC/D3. When comparing untreated controls, RNA-seq analyses showed that HBMEC have a higher expression of tight junction markers compared to hCMEC/D3. In summary, our study found that 24 h WSE treatment increases IL-8 production dose-dependently and decreases tight junction markers in both HBMEC and hCMEC/D3 that may be mediated through the AhR and NRF2 pathways, and HBMEC could be a better in vitro model for studying the effect of wood smoke extract or particles on brain endothelial cells.
野火的频率、持续时间和规模一直在增加,吸入野火烟雾颗粒对人类健康构成重大威胁。流行病学研究表明,野火烟雾暴露与认知和神经功能障碍呈正相关。然而,关于野火烟雾暴露如何影响血脑屏障并导致大脑中的分子和细胞变化,我们的知识还存在很大的差距。我们的研究旨在确定闷烧桉树木烟提取物(WSE)对体外潜在神经毒性的脑内皮细胞的急性影响。用人脑微血管内皮细胞(HBMEC)和永生化人脑内皮细胞系(hCMEC/D3)处理不同剂量的 WSE 24 小时。WSE 处理导致 HBMEC 和 hCMEC/D3 中 IL-8 呈剂量依赖性增加。RNA-seq 分析显示,WSE 处理剂量依赖性地上调了参与芳烃受体(AhR)和核因子红细胞 2 相关因子 2(NRF2)途径的基因,以及 HBMEC 和 hCMEC/D3 中紧密连接标记物的减少。与未处理的对照组相比,RNA-seq 分析显示 HBMEC 中紧密连接标记物的表达高于 hCMEC/D3。总之,我们的研究发现,24 小时 WSE 处理剂量依赖性地增加了 IL-8 的产生,并降低了 HBMEC 和 hCMEC/D3 中紧密连接标记物的表达,这可能是通过 AhR 和 NRF2 途径介导的,而 HBMEC 可能是研究木烟提取物或颗粒对脑内皮细胞影响的更好的体外模型。