Michele Davigo , Frederik Jan Van Schooten , Bas Wijnhoven , Marie Jose Drittij , Ludwig Dubois , Antoon Opperhuizen , Reinskje Talhout , Alexander H.V. Remels
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The oxygen consumption rate of differently exposed cells was measured, and mRNA and protein abundancy of key molecules involved in the molecular regulation of mitochondrial metabolism were assessed. Furthermore, we used a mitophagy detection probe to visualize mitochondrial breakdown over time in response to the extracts. Both types of extracts induced increases in basal-, maximal- and spare respiratory capacity, as well as in cellular ATP production. Moreover, we observed alterations in the abundancy of regulatory molecules controlling mitochondrial biogenesis and mitophagy. 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引用次数: 0
摘要
肺上皮细胞线粒体异常与慢性阻塞性肺病(COPD)的发病机制有关。香烟烟雾(CS)可诱导肺上皮细胞线粒体功能的分子调控途径发生改变。与普通香烟相比,加热烟草制品(HTPs)最近被作为减害产品推向市场。然而,加热烟草制品的排放对人类肺泡上皮细胞新陈代谢以及线粒体含量和功能的分子调控机制的影响尚不清楚。在这项研究中,人类肺泡上皮细胞(A549)暴露于香烟或 HTP 液态提取物形式的排放物中。测量了不同暴露细胞的耗氧率,并评估了参与线粒体代谢分子调控的关键分子的 mRNA 和蛋白质丰度。此外,我们还使用了一种有丝分裂检测探针,以观察线粒体在不同提取物作用下的分解过程。两种提取物都能诱导基础、最大和剩余呼吸能力以及细胞 ATP 生成的增加。此外,我们还观察到控制线粒体生物生成和有丝分裂的调节分子的丰度发生了变化。丝裂吞噬对提取物的反应没有明显改变,因为与车辆处理的细胞相比没有观察到显著差异。
Alterations in the molecular regulation of mitochondrial metabolism in human alveolar epithelial cells in response to cigarette- and heated tobacco product emissions
Mitochondrial abnormalities in lung epithelial cells have been associated with chronic obstructive pulmonary disease (COPD) pathogenesis. Cigarette smoke (CS) can induce alterations in the molecular pathways regulating mitochondrial function in lung epithelial cells. Recently, heated tobacco products (HTPs) have been marketed as harm reduction products compared with regular cigarettes. However, the effects of HTP emissions on human alveolar epithelial cell metabolism and on the molecular mechanisms regulating mitochondrial content and function are unclear. In this study, human alveolar epithelial cells (A549) were exposed to cigarette or HTP emissions in the form of liquid extracts. The oxygen consumption rate of differently exposed cells was measured, and mRNA and protein abundancy of key molecules involved in the molecular regulation of mitochondrial metabolism were assessed. Furthermore, we used a mitophagy detection probe to visualize mitochondrial breakdown over time in response to the extracts. Both types of extracts induced increases in basal-, maximal- and spare respiratory capacity, as well as in cellular ATP production. Moreover, we observed alterations in the abundancy of regulatory molecules controlling mitochondrial biogenesis and mitophagy. Mitophagy was not significantly altered in response to the extracts, as no significant differences compared to vehicle-treated cells were observed.