红参对暴露于城市污染物的HaCaT细胞线粒体动力学和生物能量学的影响

G. Beauchef, M. Favre-Mercuret, Beatrice Blanc, R. Fitoussi, K. Vié, N. Compagnone
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引用次数: 1

摘要

背景:城市空气污染导致肺部和心血管系统功能障碍,是人类健康的重要问题。它对皮肤完整性的影响,与特应性皮炎的发生率增加有关,现在已经认识到,但其细胞机制仍然知之甚少。目的:利用HaCaT细胞模型研究城市污染物对线粒体动力学和生物能学的影响。我们还试图建立ECH-5195(红参提取物)的保护作用,人参皂苷标准化,逆转污染诱导的线粒体缺陷。方法:采用HaCaT细胞对含多环芳烃、硝基多环芳烃、多氯联苯同系物和氯化农药的标准化大气颗粒物(平均粒径5.85 μm, SRM1648)暴露1 h的方法模拟城市污染暴露。结果:城市污染物的存在使网状线粒体网络的高分裂率增加了1.41倍(p = 0.023),裂变率增加了1.35倍(p = 0.006)。ECH-5195使线粒体网状网络正常化,使污染引起的超裂变减少0.54倍(p = 0.004),裂变减少0.68倍(p = 0.0006)。污染暴露与基础OCR的显著降低和乳酸生成的增加有关,促使细胞依赖糖酵解来产生ATP。当使用ECH-5195时,OCR显著增加,糖酵解对ATP产生的贡献减少,而氧化磷酸化和线粒体呼吸都增加,表明线粒体重新参与ATP产生。结论:污染暴露对线粒体网络动力学和线粒体呼吸都具有破坏性。ECH-5195中的人参皂苷有效地保护了两者免受污染引起的缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Red Panax ginseng on Mitochondrial Dynamics and Bioenergetics in HaCaT Cells Exposed to Urban Pollutants
Background: Urban air pollution contributes to lung and cardiovascular system dysfunction, making it a major concern for human health. Its impact on skin integrity, associated with increased occurrence of atopic dermatitis, is now recognized, but its cellular mechanisms remain poorly understood. Objective: In the present study we aimed at establishing the impact of urban pollutant on mitochondrial dynamics and bioenergetics using the HaCaT cell model. We also sought to establish the protective effect of ECH-5195 (red Panax ginseng extract), standardized in ginsenosides, in reversing pollution-induced mitochondrial defects. Methods: Urban pollution exposure was mimicked by 1 h exposure of HaCaT cells with standardized atmospheric particulate matter containing PAHs, nitro-PAHs, PCB congeners, and chlorinated pesticides with a mean particulate diameter of 5.85 μm (SRM1648). Results: The presence of urban pollutant in the cultures increased the prevalence of hyperfission by 1.41-fold (p = 0.023) and fission by 1.35 fold (p = 0.006) in the reticular mitochondrial network. ECH-5195 reduced both pollution-induced hyperfission by 0.54-fold (p = 0.004) and fission by 0.68-fold (p = 0.0006) normalizing the mitochondrial reticular network. Pollution exposure was associated with a significant reduction of basal OCR and increased lactate production, pushing the cell to rely on glycolysis for ATP production. When ECH-5195 was used, OCR was significantly increased, and the glycolytic contribution to ATP production was reduced while both oxidative phosphorylation and mitochondrial respiration were increased demonstrating mitochondrial re-engagement in ATP production. Conclusions: Pollution exposure was disruptive for both the mitochondrial network dynamics and mitochondrial respiration. Ginsenosides in ECH-5195 efficiently protected both from pollution-induced defects.
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