首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Matrix Metalloproteinase-9 Mediates the Deleterious Effects of alpha 2-Antiplasmin on Blood-Brain Barrier Breakdown and Ischemic Brain Injury in Experimental Stroke
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Matrix Metalloproteinase-9 Mediates the Deleterious Effects of alpha 2-Antiplasmin on Blood-Brain Barrier Breakdown and Ischemic Brain Injury in Experimental Stroke

机译:基质金属蛋白酶-9介导α2-抗蛋白对实验中风血脑屏障分解和缺血性脑损伤的有害影响

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During acute brain ischemia, alpha 2-antiplasmin markedly enhances brain injury, blood-brain barrier breakdown and matrix metalloproteinase-9 (MMP-9) expression. Although alpha 2-antiplasmin inhibits fibrin thrombus-degradation, and MMP-9 is a collagen-degrading enzyme altering blood-brain barrier, both have similar deleterious effects on the ischemic brain. We examined the hypothesis that MMP-9 is an essential downstream mediator of alpha 2-antiplasmin's deleterious effects during brain ischemia. Middle cerebral artery thromboembolic stroke was induced in a randomized, blinded fashion in mice with increased blood levels of a2-antiplasmin. There was a robust increase in MMP-9 expression (immunofluorescence) in the ischemic vs. the non-ischemic hemisphere of MMP-9(+/+) but not MMP-9(-/-) mice, 24 h after stroke. Brain swelling and hemorrhage were significantly increased in the ischemic vs. the non-ischemic hemisphere of MMP-9(+/+) mice. By comparison to MMP-9(+/+) mice, the ischemic hemispheres of MMP-9(-/-) mice showed a similar to 6-fold reduction in brain swelling (p 0.001) and a similar to 9fold reduction in brain hemorrhage. Brain infarction (p 0.0001) and TUNEL-positive cell death (p 0.001) were significantly diminished in the ischemic hemisphere of MMP-9(-/-) mice vs. MMP-9(+/+) mice. Ischemic breakdown of the blood-brain barrier and fibrin deposition were also significantly reduced in MMP-9(-/-) mice vs. MMP-9(+/+) mice (p 0.05), as measured by quantitative immunofluorescence. We conclude that MMP-9 deficiency ablates many of the deleterious effects of high alpha 2-antiplasmin levels, significantly reducing blood-brain barrier breakdown, TUNEL-positive cell death, brain hemorrhage, swelling and infarction. This suggests that the two molecules may be in a shared pathway in which MMP-9 is essential downstream for the deleterious effects of a2-antiplasmin in ischemic stroke. (C) 2018 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:在急性脑缺血,α-2-抗纤溶酶显着增强了脑损伤,血 - 脑屏障的破坏和基质金属蛋白酶-9(MMP-9)的表达。虽然阿尔法2 - 抗纤溶酶抑制纤维蛋白血栓分解,和MMP-9是胶原降解酶改变血 - 脑屏障,既对缺血性脑类似的有害作用。我们研究的假设,MMP-9是脑缺血时的α2 - 抗纤溶酶的有害作用的重要下游介质。大脑中动脉血栓栓塞性中风是在一个随机,双盲的方式诱导小鼠α2 - 抗血水平增加。有在缺血与一个强劲增长MMP-9的表达(免疫荧光)MMP-9的非缺血性半球(+ / +),但不MMP-9( - / - )小鼠,中风后24小时。脑肿胀和出血缺血与均显著增加MMP-9(+ / +)小鼠的非缺血性半球。通过比较MMP-9(+ / +)小鼠中,MMP-9的缺血性半球( - / - )小鼠显示出类似于脑6倍的减少肿胀(P< 0.001)和一个类似于9fold减少脑出血。脑梗塞(P< 0.0001)和TUNEL阳性细胞死亡(P< 0.001)( - / - )小鼠对MMP-9(+ / +)小鼠中MMP-9的缺血性半球均显著减少。如通过定量免疫测定;(0.05 P&LT)( - / - )小鼠对MMP-9(+ / +)小鼠中的血 - 脑屏障的和纤维蛋白沉积缺血击穿也显著在MMP-9降低。我们的结论是MMP-9缺乏消融许多的高α2 - 抗纤溶酶水平的有害影响,显著降低血 - 脑屏障的破坏,TUNEL阳性细胞死亡,脑出血,肿胀和梗塞。这表明两种分子可以是在一个共享的途径,其中MMP-9是用于α2 - 抗纤溶酶的缺血性中风的有害作用必不可少下游。 (c)2018年IBRO。 elsevier有限公司出版。保留所有权利。

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