Kafoury Ramzi M, Madden Michael C
Center of Environmental Health and Molecular Toxicology Laboratory, Jackson State University, Jackson, Mississippi, USA.
Int J Environ Res Public Health. 2005 Apr;2(1):107-13. doi: 10.3390/ijerph2005010107.
Exposure to particulate matter (PM2.5-10), including diesel exhaust particles (DEP) has been reported to induce lung injury and exacerbation of asthma and chronic obstructive pulmonary disease. Alveolar macrophages play a major role in the lung's response to inhaled particles and therefore, are a primary target for PM2.5-10 effect. The molecular and cellular events underlying DEP-induced toxicity in the lung, however, remain unclear. To determine the effect of DEP on alveolar macrophages, RAW 264.7 cells were grown in RPMI 1640 with supplements until confluency. RAW 264.7 cultures were exposed to Hank's buffered saline solution (vehicle), vehicle containing an NF-kappaB inhibitor, BAY11-7082 (25 microM with 11/2 hr pre-incubation), or vehicle containing DEP (250 microg/ml) in the presence or absence of BAY11-7082 (25 microM with 11/2 hr pre-incubation) for 4 hr and TNF-alpha release was determined by enzyme-linked immunosorbent assay and confirmed by western blots. RAW 264.7 apoptotic response was determined by DNA fragmentation assays. U937 cells treated with campothecin (4 microg/ml x 3 hr), an apoptosis-inducing agent, were used as positive control. We report that exposure to the carbonaceous core of DEP induces significant release of TNF-alpha in a concentration-dependent fashion (31 +/- 4 pg/ml, n = 4, p = 0.08; 162 +/- 23 pg/ml, n = 4, p < 0.05; 313 +/- 31 pg/ml, n = 4, p < 0.05 at 25, 100, and 250 microg/ml, respectively). DEP exposure, however, failed to induce any apoptotic response in RAW 264.7 cells. Moreover, inhibition of NF-kappaB binding activity has resulted in DEP-induced apoptotic response in alveolar macrophages, as demonstrated by the NF-kappaB inhibitor, BAY11-7082 studies. The results of the present study indicate that DEP induce the release of TNF-alpha in alveolar macrophages, a primary target for inhaled particles effect. DEP-induced TNF-alpha gene expression is regulated at the transcriptional level by NF-kappaB. Furthermore, DEP-induced increase in NF-kappaB-DNA binding activity appears to protect against apoptosis.
据报道,接触包括柴油废气颗粒(DEP)在内的颗粒物(PM2.5 - 10)会导致肺损伤以及哮喘和慢性阻塞性肺疾病的加重。肺泡巨噬细胞在肺部对吸入颗粒的反应中起主要作用,因此是PM2.5 - 10作用的主要靶点。然而,DEP诱导肺部毒性的分子和细胞事件仍不清楚。为了确定DEP对肺泡巨噬细胞的影响,将RAW 264.7细胞在含有补充剂的RPMI 1640培养基中培养至汇合。RAW 264.7培养物在存在或不存在BAY11 - 7082(25 microM,预孵育1.5小时)的情况下,暴露于汉克平衡盐溶液(载体)、含有NF-κB抑制剂BAY11 - 7082的载体(25 microM,预孵育1.5小时)或含有DEP(250 microg/ml)的载体中4小时,并通过酶联免疫吸附测定法测定TNF-α释放,并通过蛋白质印迹法进行确认。通过DNA片段化测定法确定RAW 264.7细胞的凋亡反应。用喜树碱(4 microg/ml×3小时)处理的U937细胞,一种凋亡诱导剂,用作阳性对照。我们报告说,接触DEP的碳质核心以浓度依赖性方式诱导TNF-α的显著释放(分别在25、100和250 microg/ml时为31±4 pg/ml,n = 4,p = 0.08;162±23 pg/ml,n = 4,p < 0.05;313±31 pg/ml,n = 4,p < 0.05)。然而,DEP暴露未能在RAW 264.7细胞中诱导任何凋亡反应。此外,如NF-κB抑制剂BAY11 - 7082研究所示,抑制NF-κB结合活性导致肺泡巨噬细胞中DEP诱导的凋亡反应。本研究结果表明,DEP诱导肺泡巨噬细胞中TNF-α的释放,肺泡巨噬细胞是吸入颗粒作用的主要靶点。DEP诱导的TNF-α基因表达在转录水平受NF-κB调节。此外,DEP诱导的NF-κB-DNA结合活性增加似乎可防止细胞凋亡。