Planas A M, Solé S, Justicia C, Farré E R
Departament de Farmacologia i Toxicologia, Institut d'Investigacions Biomèdiques de Barcelona, Barcelona, E-08036, Spain.
Biochem Biophys Res Commun. 2000 Nov 30;278(3):803-7. doi: 10.1006/bbrc.2000.3881.
Matrix metalloproteinases degrade the extracellular matrix and are involved in a variety of diseases, including inflammatory diseases of the central nervous system. Here we estimated the content of gelatinase in rat brain under control conditions and 4 h after transient focal ischemia using gelatinolytic extraction and zymographic analysis. We also examined the expression of the MMP-9 and MMP-2 proteins by Western blot. Using the zymographic apparent gelatinase activity we estimated that brain gelatinase content was 0.44 ng/mg of protein. Ischemia induced a 1.7-fold increase at 4 h, thus showing an early MMP response to the ischemic injury. The main increase was seen for the MMP-9 proform, which was accompanied by enhanced MMP-9 protein expression. We suggest that basal cerebral MMP-9 and MMP-2 activities are involved in the maintenance of the extracellular matrix and prevent substrate accumulation, while enhanced postischemic MMP activity before cell death may contribute to edema formation and blood-brain barrier breakdown.
基质金属蛋白酶可降解细胞外基质,并参与多种疾病,包括中枢神经系统的炎症性疾病。在此,我们通过明胶酶解提取和酶谱分析,估计了正常对照条件下以及短暂局灶性缺血4小时后大鼠脑中明胶酶的含量。我们还通过蛋白质印迹法检测了MMP-9和MMP-2蛋白的表达。利用酶谱分析的表观明胶酶活性,我们估计脑明胶酶含量为0.44 ng/mg蛋白质。缺血在4小时时导致其增加了1.7倍,从而显示出MMP对缺血损伤的早期反应。主要增加的是MMP-9前体形式,同时伴有MMP-9蛋白表达增强。我们认为,脑基底MMP-9和MMP-2活性参与细胞外基质的维持并防止底物积累,而细胞死亡前缺血后MMP活性增强可能导致水肿形成和血脑屏障破坏。