Kim Ji Young, Oh Kyo Nyeo, Han Eun Hee, Kim Dong Hee, Jeong Tae Cheon, Lee Eung Seok, Jeong Hye Gwang
Department of Pharmacy, College of Pharmacy, Research Center for Proteineous Materials, Chosun University, Kwangju, Republic of Korea.
Biochem Biophys Res Commun. 2005 Aug 12;333(4):1234-40. doi: 10.1016/j.bbrc.2005.06.038.
Methoxychlor (MXC) is a pesticide that was developed as a replacement for dichlorodiphenyltrichloroethane. The influence of MXC on cytokine production or the functions of macrophages is unclear. This study examined the effects of MXC on the production of nitric oxide (NO) and the proinflammatory cytokines (IL-1beta, IL-6, and TNF-alpha), and analyzed the molecular mechanism in mouse macrophages. The addition of MXC to macrophages induced the production of NO and proinflammatory cytokines and expression levels of these genes in a dose-dependent manner. The NF-kappaB sites were identified in the promoter of the iNOS and proinflammatory cytokines genes. The transient expression and electrophoretic mobility shift assays revealed that the NF-kappaB transcription factor mediated the MXC-induced increase in the iNOS and proinflammatory cytokines expression levels. In addition, MXC induced the rapid phosphorylation of the ERK1/2 and p38 MAPK. This demonstrates that MXC stimulates the production of NO and proinflammatory cytokines and can up-regulate the expression levels of these genes via NF-kappaB transactivation and ERK1/2 and p38 MAPK phosphorylation. Overall, this study provides evidence showing that MXC has inflammatory potential that is previously unrecognized immunomodulating activity.
甲氧滴滴涕(MXC)是一种作为二氯二苯三氯乙烷替代品而研发的杀虫剂。MXC对细胞因子产生或巨噬细胞功能的影响尚不清楚。本研究检测了MXC对一氧化氮(NO)和促炎细胞因子(IL-1β、IL-6和TNF-α)产生的影响,并分析了其在小鼠巨噬细胞中的分子机制。向巨噬细胞中添加MXC以剂量依赖的方式诱导了NO和促炎细胞因子的产生以及这些基因的表达水平。在诱导型一氧化氮合酶(iNOS)和促炎细胞因子基因的启动子中鉴定出了核因子κB(NF-κB)位点。瞬时表达和电泳迁移率变动分析表明,NF-κB转录因子介导了MXC诱导的iNOS和促炎细胞因子表达水平的增加。此外,MXC诱导了细胞外信号调节激酶1/2(ERK1/2)和p38丝裂原活化蛋白激酶(p38 MAPK)的快速磷酸化。这表明MXC刺激了NO和促炎细胞因子的产生,并可通过NF-κB反式激活以及ERK1/2和p38 MAPK磷酸化上调这些基因的表达水平。总体而言,本研究提供的证据表明,MXC具有先前未被认识到的免疫调节活性的炎症潜力。