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外源性物质通过p38丝裂原活化蛋白激酶信号通路诱导肿瘤坏死因子-α表达和细胞凋亡。

Xenobiotic-induced TNF-alpha expression and apoptosis through the p38 MAPK signaling pathway.

作者信息

Frigo Daniel E, Vigh Katinka A, Struckhoff Amanda P, Elliott Steven, Beckman Barbara S, Burow Matthew E, McLachlan John A

机构信息

Center for Bioenvironmental Research, Molecular and Cellular Biology Program, Tulane University Health Science Center, New Orleans, LA 70112, USA.

出版信息

Toxicol Lett. 2005 Feb 15;155(2):227-38. doi: 10.1016/j.toxlet.2004.09.008.

Abstract

Some xenobiotics, such as dichlorodiphenyltrichloroethane (DDT), bind to and activate estrogen receptors (ERs), eliciting estrogenic effects in both wildlife and humans. However, our laboratory and others have demonstrated that DDT and DDT-like compounds target non-ER pathways. In search for a molecular mechanism we recently established that DDT and its metabolites stimulate activator protein-1 (AP-1)-mediated gene expression through the p38 mitogen-activated protein kinase (MAPK) cascade. Here, we determined that DDT-induced p38 activity produces a novel environmental signaling pathway in endometrial Ishikawa and human embryonic kidney (HEK) 293 cells. Xenobiotic exposure stimulates expression of the death ligand, tumor necrosis factor-alpha (TNF-alpha) as demonstrated using RT-PCR and reporter gene assays. Furthermore, DDT-induced p38 activity led to the release of cytochrome c from the mitochondria and activation of caspase-3/7. Ultimately, DDT-treated cells underwent cell death. Taken together, these data demonstrate DDT induces both the expression of the death ligand TNF-alpha and apoptosis through a p38 MAPK-dependent mechanism.

摘要

一些外源性物质,如滴滴涕(DDT),会与雌激素受体(ERs)结合并激活它们,从而在野生动物和人类中引发雌激素效应。然而,我们实验室及其他研究团队已证明,DDT及类似DDT的化合物靶向非雌激素受体途径。为探寻分子机制,我们最近证实,DDT及其代谢产物通过p38丝裂原活化蛋白激酶(MAPK)级联反应刺激活化蛋白-1(AP-1)介导的基因表达。在此,我们确定DDT诱导的p38活性在子宫内膜 Ishikawa 细胞和人胚肾(HEK)293 细胞中产生了一条新的环境信号通路。如通过逆转录聚合酶链反应(RT-PCR)和报告基因检测所示,外源性物质暴露会刺激死亡配体肿瘤坏死因子-α(TNF-α)的表达。此外,DDT诱导的p38活性导致细胞色素c从线粒体释放,并激活半胱天冬酶-3/7。最终,经DDT处理的细胞发生细胞死亡。综上所述,这些数据表明DDT通过p38 MAPK依赖性机制诱导死亡配体TNF-α的表达及细胞凋亡。

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