Department of Pharmacology, Chang Gung University, 259 Wen-Hwa 1st Road, Kwei-San, Tao-Yuan, Taiwan.
Neurotox Res. 2010 Jan;17(1):50-65. doi: 10.1007/s12640-009-9077-2. Epub 2009 Jun 25.
After ischemic injury to brain, disruption of the blood-brain barrier (BBB) raises the possibility of exposing the central nervous system (CNS) to oxidized low-density lipoprotein (oxLDL), a risk factor implicated in neurodegenerative diseases. Matrix metalloproteinases (MMPs), especially MMP-9, contribute to extracellular matrix (ECM) remodeling during the CNS diseases. However, the molecular mechanisms underlying oxLDL-induced MMP-9 expression in astrocytes remained unclear. Here, we reported that oxLDL induced MMP-9 expression via a PKC-delta/p42/p44 MAPK-dependent Elk-1 activation in rat brain astrocyte (RBA)-1 cells, revealed by gelatin zymography, RT-PCR, and Western blotting analyses. These responses were attenuated by pretreatment with pharmacological inhibitors and transfection with dominant negative mutants. Moreover, Elk-1-mediated MMP-9 gene transcription was confirmed by transfection with an Elk-1 binding site-mutated MMP-9 promoter construct (mt-Ets-MMP9), which blocked oxLDL-stimulated MMP-9 luciferase activity. Understanding the regulatory mechanisms by which oxLDL induced MMP-9 expression in astrocytes might provide a new therapeutic strategy of brain diseases.
脑缺血损伤后,血脑屏障(BBB)的破坏使中枢神经系统(CNS)有可能暴露于氧化型低密度脂蛋白(oxLDL),这是一种与神经退行性疾病有关的危险因素。基质金属蛋白酶(MMPs),特别是 MMP-9,在 CNS 疾病期间有助于细胞外基质(ECM)的重塑。然而,oxLDL 诱导星形胶质细胞中 MMP-9 表达的分子机制尚不清楚。在这里,我们通过明胶酶谱分析、RT-PCR 和 Western blot 分析报告了 oxLDL 通过 PKC-delta/p42/p44 MAPK 依赖性 Elk-1 激活诱导星形胶质细胞(RBA-1 细胞)中 MMP-9 的表达。这些反应通过用药理抑制剂预处理和转染显性负突变体而减弱。此外,通过转染 Elk-1 结合位点突变的 MMP-9 启动子构建体(mt-Ets-MMP9)证实了 Elk-1 介导的 MMP-9 基因转录,该构建体阻断了 oxLDL 刺激的 MMP-9 荧光素酶活性。了解 oxLDL 诱导星形胶质细胞中 MMP-9 表达的调节机制可能为脑部疾病提供新的治疗策略。