Ito Tsuyoshi, Okumura Hiroki, Tsukue Naomi, Kobayashi Takahiro, Honda Katsuya, Sekizawa Kiyohisa
Graduate School of Comprehensive Human Sciences, University of Tsukuba, 1-1-1 Tennohdai, Tsukuba, Ibaraki 305-8575, Japan.
Toxicol Lett. 2006 Aug 1;165(1):66-70. doi: 10.1016/j.toxlet.2006.01.015. Epub 2006 Feb 28.
Epidemiological studies have shown that particulate matter (PM) is associated with adverse respiratory health effects. Although infection in the respiratory organ is one of the most important health risks the association of infection with PM is not fully understood. As we had hypothesized that diesel exhaust particles (DEP), one of the major component of PM, may induce the expression of receptors for viruses and bacteria at invasion sites, we studied the effect of DEP on the mRNA expression of intercellular adhesion molecule-1 (ICAM-1), low-density lipoprotein (LDL) and platelet-activating factor (PAF) receptors, which are invasion sites of virus and bacteria, on rat lung epithelial cells. The real-time quantitative polymerase chain reaction (PCR) method was used for the evaluation. All of these mRNAs were up-regulated by 3, 10, and 30 microg/ml of DEP in a concentration-dependent manner. The up-regulation of each was associated with the mRNA expression of heme oxygenase-1 (HO-1), a marker of oxidative stress. Our present results show that DEP up-regulated the mRNA expression of viral and bacterial receptors. This up-regulation might be associated with DEP-induced oxidative stress. These results thus suggest that DEP may enhance the risk of pneumonia by increasing the density of bacterial and viral invasion sites in the lungs.
流行病学研究表明,颗粒物(PM)与呼吸道健康不良影响有关。尽管呼吸道器官感染是最重要的健康风险之一,但感染与PM之间的关联尚未完全明确。由于我们曾假设PM的主要成分之一柴油尾气颗粒(DEP)可能会诱导病毒和细菌受体在入侵部位的表达,因此我们研究了DEP对大鼠肺上皮细胞中细胞间黏附分子-1(ICAM-1)、低密度脂蛋白(LDL)和血小板活化因子(PAF)受体mRNA表达的影响,这些都是病毒和细菌的入侵部位。采用实时定量聚合酶链反应(PCR)方法进行评估。所有这些mRNA均以浓度依赖的方式被3、10和30微克/毫升的DEP上调。每种mRNA的上调都与氧化应激标志物血红素加氧酶-1(HO-1)的mRNA表达有关。我们目前的结果表明,DEP上调了病毒和细菌受体的mRNA表达。这种上调可能与DEP诱导的氧化应激有关。因此,这些结果表明,DEP可能通过增加肺部细菌和病毒入侵部位的密度来增加肺炎风险。