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Hypoxia-controlled matrix metalloproteinase-9 hyperexpression promotes behavioral recovery after ischemia

机译:缺氧控制的基质金属蛋白酶9过度表达促进缺血后的行为恢复

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摘要

Matrix metalloproteinase-9 (MMP-9) plays a beneficial role in the sub-acute phase after ischemic stroke. However, unrestrained MMP-9 may disrupt the blood-brain barrier (BBB), which has limited its use for the treatment of brain ischemia. In the present study, we constructed lentivirus mediated hypoxia-controlled MMP-9 expression and explored its role after stroke. Hypoxia response element (HRE) was used to confine MMP-9 expression only to the hypoxic region of mouse brain after 120-min transient middle cerebral artery occlusion. Lentiviruses were injected into the peri-infarct area on day 7 after transient ischemia. We found hyperexpression of exogenous HRE-MMP-9 under the control of hypoxia, and its expression was mainly located in neurons and astrocytes without aggravation of BBB damage compared to the CMV group. Furthermore, mice in the HRE-MMP-9 group showed the best behavioral recovery compared with the normal saline, GFP, and SB-3CT groups. Therefore, hypoxia-controlled MMP-9 hyperexpression during the sub-acute phase of ischemia may provide a novel promising approach of gene therapy for stroke.Electronic Supplementary MaterialSupplementary material is available for this article at 10.1007/s12264-015-1533-1 and is accessible for authorized users.
机译:基质金属蛋白酶9(MMP-9)在缺血性中风后的亚急性期起有益作用。但是,不受限制的MMP-9可能会破坏血脑屏障(BBB),从而限制了其在治疗脑缺血中的用途。在本研究中,我们构建了慢病毒介导的缺氧控制的MMP-9表达,并探讨了其在中风后的作用。缺氧反应元件(HRE)用于将MMP-9表达仅限制在120分钟短暂性大脑中动脉闭塞后的小鼠脑缺氧区域。在短暂性缺血后第7天,将慢病毒注射入梗塞周围区域。我们发现外源性HRE-MMP-9的高表达在缺氧的控制下,与CMV组相比,其表达主要位于神经元和星形胶质细胞中,而不会加重BBB损伤。此外,与生理盐水,GFP和SB-3CT组相比,HRE-MMP-9组的小鼠表现出最佳的行为恢复。因此,在缺血亚急性期低氧控制的MMP-9高表达可能为脑卒中的基因治疗提供了一种新的有前途的方法。电子补充材料本文提供的补充材料为10.1007 / s12264-015-1533-1,授权用户可以访问。

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