Department of Biomedical Laboratory Science, College of Health Science, Eulji University, Seongnam, 461-713 Gyeonggi-Do, South Korea.
Mol Biol Rep. 2012 Mar;39(3):3001-7. doi: 10.1007/s11033-011-1062-1. Epub 2011 Jun 17.
Foam cells derived from macrophages have been implicated as markers of early stage atherosclerosis development. In this study, we found that N-acetyl cysteine (NAC), a well-known inhibitor of reactive oxygen species (ROS), decreased the generation of ROS and suppressed foam cell formation in the presence of oxidized low density lipoprotein through down-regulation of cluster of differentiation 36 expression. We investigated gene expression profiles in order to determine the effects of NAC on foam cell formation using a microarray analysis. The level of apolipoprotein E, which is involved in lipid efflux, was increased and the levels of the antioxidant genes glutathione peroxidase 1 and 3 were also increased. The expression levels of the oxidative stress response and the DNA repair genes were decreased. These results were confirmed using quantitative real-time PCR. Our results indicate that oxidative stress plays an important role in foam cell formation, and that regulation of oxidation using antioxidants is a potential therapeutic method for blocking atherosclerosis development.
泡沫细胞来源于巨噬细胞,被认为是动脉粥样硬化早期发展的标志物。在这项研究中,我们发现 N-乙酰半胱氨酸(NAC),一种众所周知的活性氧(ROS)抑制剂,通过下调 CD36 表达,减少 ROS 的产生,并抑制氧化低密度脂蛋白存在时的泡沫细胞形成。我们通过微阵列分析研究基因表达谱,以确定 NAC 对泡沫细胞形成的影响。参与脂质外排的载脂蛋白 E 的水平增加,抗氧化基因谷胱甘肽过氧化物酶 1 和 3 的水平也增加。氧化应激反应和 DNA 修复基因的表达水平降低。这些结果通过定量实时 PCR 得到了证实。我们的结果表明,氧化应激在泡沫细胞形成中起重要作用,使用抗氧化剂调节氧化是阻止动脉粥样硬化发展的一种潜在治疗方法。