Department of Environmental and Molecular Toxicology, North Carolina State University, Raleigh, NC 27695-7633, USA.
Am J Respir Cell Mol Biol. 2012 Oct;47(4):552-61. doi: 10.1165/rcmb.2012-0023OC. Epub 2012 Jun 14.
Pleural diseases (fibrosis and mesothelioma) are a major concern for individuals exposed by inhalation to certain types of particles, metals, and fibers. Increasing attention has focused on the possibility that certain types of engineered nanoparticles (NPs), especially those containing nickel, might also pose a risk for pleural diseases. Platelet-derived growth factor (PDGF) is an important mediator of fibrosis and cancer that has been implicated in the pathogenesis of pleural diseases. In this study, we discovered that PDGF synergistically enhanced nickel NP (NiNP)-induced increases in mRNA and protein levels of the profibrogenic chemokine monocyte chemoattractant protein-1 (MCP-1 or CCL2), and the antifibrogenic IFN-inducible CXC chemokine (CXCL10) in normal rat pleural mesothelial 2 (NRM2) cells in vitro. Carbon black NPs (CBNPs), used as a negative control NP, did not cause a significant increase in CCL2 or CXCL10 in the absence or presence of PDGF. NiNPs prolonged PDGF-induced phosphorylation of the mitogen-activated protein kinase family termed extracellular signal-regulated kinases (ERK)-1 and -2 for up to 24 hours, and NiNPs also synergistically increased PDGF-induced hypoxia-inducible factor (HIF)-1α protein levels in NRM2 cells. Inhibition of ERK-1,2 phosphorylation with the mitogen-activated protein kinase kinase (MEK) inhibitor, PD98059, blocked the synergistic increase in CCL2, CXCL10, and HIF-1α levels induced by PDGF and NiNPs. Moreover, the antioxidant, N-acetyl-L-cysteine (NAC), significantly reduced HIF-1α, ERK-1,2 phosphorylation, and CCL2 protein levels that were synergistically increased by the combination of PDGF and NiNPs. These data indicate that NiNPs enhance the activity of PDGF in regulating chemokine production in NRM2 cells through a mechanism involving reactive oxygen species generation and prolonged activation of ERK-1,2.
胸膜疾病(纤维化和间皮瘤)是某些类型的颗粒、金属和纤维吸入暴露个体的主要关注点。人们越来越关注某些类型的工程纳米颗粒(NPs),特别是那些含有镍的 NPs,也可能对胸膜疾病构成风险。血小板衍生生长因子(PDGF)是纤维化和癌症的重要介质,已被牵连到胸膜疾病的发病机制中。在这项研究中,我们发现 PDGF 协同增强镍纳米颗粒(NiNP)诱导的正常大鼠胸膜间皮 2(NRM2)细胞中致纤维化趋化因子单核细胞趋化蛋白-1(MCP-1 或 CCL2)和抗纤维化 IFN 诱导的 CXC 趋化因子(CXCL10)的 mRNA 和蛋白水平。作为阴性对照 NP 的炭黑 NPs(CBNPs)在不存在或存在 PDGF 的情况下不会导致 CCL2 或 CXCL10 显著增加。NiNPs 使 PDGF 诱导的丝裂原活化蛋白激酶家族成员细胞外信号调节激酶(ERK)-1 和 -2 的磷酸化延长至 24 小时,并且 NiNPs 还协同增加了 NRM2 细胞中 PDGF 诱导的缺氧诱导因子(HIF)-1α蛋白水平。用丝裂原活化蛋白激酶激酶(MEK)抑制剂 PD98059 抑制 ERK-1,2 磷酸化,阻断了 PDGF 和 NiNPs 协同诱导的 CCL2、CXCL10 和 HIF-1α水平的增加。此外,抗氧化剂 N-乙酰-L-半胱氨酸(NAC)显著降低了 PDGF 和 NiNPs 协同增加的 HIF-1α、ERK-1,2 磷酸化和 CCL2 蛋白水平。这些数据表明,NiNPs 通过涉及活性氧生成和 ERK-1,2 延长激活的机制,增强 PDGF 在调节 NRM2 细胞中趋化因子产生中的活性。