Fujimura M, Gasche Y, Morita-Fujimura Y, Massengale J, Kawase M, Chan P H
Department of Neurosurgery, Program in Neurosciences, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Brain Res. 1999 Sep 18;842(1):92-100. doi: 10.1016/s0006-8993(99)01843-0.
Blood-brain barrier (BBB) disruption is thought to play a critical role in the pathophysiology of ischemia/reperfusion. Matrix metalloproteinases (MMPs) are a family of proteolytic enzymes that can degrade all the components of the extracellular matrix when they are activated. Gelatinase A (MMP-2) and gelatinase B (MMP-9) are able to digest the endothelial basal lamina, which plays a major role in maintaining BBB impermeability. The present study examined the expression and activation of gelatinases before and after transient focal cerebral ischemia (FCI) in mice. Adult male CD1 mice were subjected to 60 min FCI and reperfusion. Zymography was performed from 1 to 23 h after reperfusion using the protein extraction method with detergent extraction and affinity-support purification. MMP-9 expression was also examined by both immunohistochemistry and Western blot analysis, and tissue inhibitors to metalloproteinase-1 was measured by reverse zymography. The BBB opening was evaluated by the Evans blue extravasation method. The 88-kDa activated MMP-9 was absent from the control specimens, while it appeared 3 h after transient ischemia by zymography. At this time point, the BBB permeability alteration was detected in the ischemic brain. Both pro-MMP-9 (96 kDa) and pro-MMP-2 (72 kDa) were seen in the control specimens, and were markedly increased after FCI. A significant induction of MMP-9 was confirmed by both immunohistochemistry and Western blot analysis. The early appearance of activated MMP-9, associated with evidence of BBB permeability alteration, suggests that activation of MMP-9 contributes to the early formation of vasogenic edema after transient FCI.
血脑屏障(BBB)破坏被认为在缺血/再灌注的病理生理学中起关键作用。基质金属蛋白酶(MMPs)是一类蛋白水解酶,激活后可降解细胞外基质的所有成分。明胶酶A(MMP-2)和明胶酶B(MMP-9)能够消化内皮基膜,而内皮基膜在维持血脑屏障的不透性方面起主要作用。本研究检测了小鼠短暂性局灶性脑缺血(FCI)前后明胶酶的表达和激活情况。成年雄性CD1小鼠接受60分钟的FCI并进行再灌注。再灌注后1至23小时,采用去污剂提取和亲和支持纯化的蛋白质提取方法进行酶谱分析。还通过免疫组织化学和蛋白质印迹分析检测MMP-9的表达,并通过反向酶谱法测定金属蛋白酶-1的组织抑制剂。通过伊文思蓝外渗法评估血脑屏障的开放情况。对照标本中未检测到88 kDa的活化MMP-9,而酶谱分析显示短暂缺血后3小时出现该蛋白。此时,在缺血脑中检测到血脑屏障通透性改变。对照标本中可见前MMP-9(96 kDa)和前MMP-2(72 kDa),FCI后明显增加。免疫组织化学和蛋白质印迹分析均证实MMP-9有显著诱导。活化MMP-9的早期出现与血脑屏障通透性改变的证据相关,提示MMP-9的激活有助于短暂性FCI后血管源性水肿的早期形成。