Research Institute of Science for Safety and Sustainability, National Institute of Advanced Industrial Science and Technology (AIST), Onogawa 16-1, Tsukuba, Ibaraki 305-8569, Japan.
Toxicology. 2010 Jul-Aug;274(1-3):34-41. doi: 10.1016/j.tox.2010.05.004. Epub 2010 May 13.
The use of C(60) fullerenes is expected to increase in various industrial fields. Little is known about the potential toxicological mechanism of action of water-soluble C(60) fullerenes. In our previous research, gene expression profiling of the rat lung was performed after whole-body inhalation exposure to C(60) fullerenes to gain insights into the molecular events. These DNA microarray-based data closely matched the pathological findings that C(60) fullerenes caused no serious adverse pulmonary effects under the inhalation exposure condition. Taking advantage of this, we attempted to characterize time-dependent changes in the gene expression profiles after intratracheal instillation with C(60) fullerenes at different dosages and to identify the candidate expressed genes as potential biomarkers. The hierarchical cluster analysis revealed that the up- or downregulation of genes after intratracheal instillation with 1.0 mg C(60) fullerene particles in rat lung tissue was significantly over-represented in the "response to stimulus" and "response to chemical stimulus" categories of biological processes and in the "extracellular space" category of the cellular component. These results were remarkable for 1 week after the instillation with C(60) fullerenes. In the lung tissues instilled with 1.0 mg C(60) fullerene particles, many representative genes involved in "inflammatory response," such as the Cxcl2, Cxcl6, Orm1, and Spp1 genes, and in "matrix metalloproteinase activity," such as the Mmp7 and Mmp12 genes, were upregulated for over 6 months. The expression levels of 89 and 21 genes were positively correlated with the C(60) fullerene dose at 1 week and 6 months after the instillation, respectively. Most of them were involved in "inflammatory response", and the Ccl17, Ctsk, Cxcl2, Cxcl6, Lcn6, Orm1, Rnase9, Slc26a4, Spp1, Mmp7, and Mmp12 genes were overlapped. Meanwhile, the expression levels of 16 and 4 genes were negatively correlated with the C(60) fullerene dose at 1 week and 6 months after the instillation, respectively. Microarray-based gene expression profiling suggested that the expression of some genes is correlated with the dose of intratracheally instilled C(60) fullerenes. We propose that these genes are useful for identifying potential biomarkers in acute-phase or persistent responses to C(60) fullerenes in the lung tissue.
C(60) 富勒烯的应用预计将在各个工业领域增加。关于水溶性 C(60) 富勒烯的潜在毒理学作用机制知之甚少。在我们之前的研究中,通过全身吸入暴露于 C(60) 富勒烯来进行大鼠肺的基因表达谱分析,以深入了解分子事件。这些基于 DNA 微阵列的数据与病理学发现非常吻合,即在吸入暴露条件下,C(60) 富勒烯不会引起严重的肺部不良反应。利用这一点,我们试图在不同剂量下经气管内滴注 C(60) 富勒烯后,描述基因表达谱的时间依赖性变化,并确定候选表达基因作为潜在的生物标志物。层次聚类分析表明,经气管内滴注 1.0mg C(60) 富勒烯颗粒后,大鼠肺组织中基因的上调或下调在“对刺激的反应”和“对化学刺激的反应”生物过程类别以及“细胞外空间”细胞成分类别中显著过度代表。这些结果在经 C(60) 富勒烯滴注后 1 周时非常显著。在滴注 1.0mg C(60) 富勒烯颗粒的肺组织中,许多参与“炎症反应”的代表性基因,如 Cxcl2、Cxcl6、Orm1 和 Spp1 基因,以及参与“基质金属蛋白酶活性”的基因,如 Mmp7 和 Mmp12 基因,上调超过 6 个月。在滴注后 1 周和 6 个月时,89 个和 21 个基因的表达水平与 C(60) 富勒烯剂量呈正相关。它们大多数参与“炎症反应”,Ccl17、Ctsk、Cxcl2、Cxcl6、Lcn6、Orm1、Rnase9、Slc26a4、Spp1、Mmp7 和 Mmp12 基因重叠。同时,在滴注后 1 周和 6 个月时,16 个和 4 个基因的表达水平与 C(60) 富勒烯剂量呈负相关。基于微阵列的基因表达谱分析表明,一些基因的表达与气管内滴注 C(60) 富勒烯的剂量有关。我们提出,这些基因可用于识别肺组织中对 C(60) 富勒烯的急性或持续性反应的潜在生物标志物。