首页> 外文期刊>Journal of Neuroscience Research >Intracerebral transplantation of bone marrow stromal cells ameliorates tissue plasminogen activator-induced brain damage after cerebral ischemia in mice detected by in vivo and ex vivo optical imaging
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Intracerebral transplantation of bone marrow stromal cells ameliorates tissue plasminogen activator-induced brain damage after cerebral ischemia in mice detected by in vivo and ex vivo optical imaging

机译:体内和离体光学成像检测的小鼠脑缺血后骨髓基质细胞的脑内移植改善了组织纤溶酶原激活物诱导的脑损伤

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摘要

Detection and protection of the neurovascular unit (NVU) are essential for treatment of acute stroke patients, especially the use of tissue plasminogen activator (tPA). In the present study, we conducted in vivo and ex vivo optical imaging for detecting activation of matrix metalloproteinases (MMPs) and evaluated the protective effect of intracerebral transplantation of bone marrow stromal cells (BMSCs) obtained from green fluorescent protein (GFP) transgenic (Tg) mice on the NVU in tPA-mediated brain damage after transient middle cerebral artery occlusion (tMCAO) in mice. Compared with the tMCAO group, the tMCAO plus BMSC group showed significant reductions of in vivo and ex vivo fluorescent signals for MMPs at 48 hr after tMCAO, with a partial colocalization of BMSC-GFP signals. Intracerebrally transplanted BMSCs ameliorated MMP-9 activation by immunohistochemistry and Western blot with differentiation into microglial and astroglial cells. Double-immunofluorescence study revealed improved NVU disruption in the tMCAO plus BMSC group. The present study suggests that intracerebral BMSC transplantation reduced MMP activation and subsequent NVU disruption caused by tPA after tMCAO and that this MMP activation and BMSC effect were detectable with in vivo and ex vivo optical imaging.
机译:神经血管单位(NVU)的检测和保护对于治疗急性中风患者至关重要,尤其是组织纤溶酶原激活剂(tPA)的使用。在本研究中,我们进行了体内和体外光学成像以检测基质金属蛋白酶(MMP)的活化,并评估了从绿色荧光蛋白(GFP)转基因(Tg)获得的骨髓基质细胞(BMSC)的脑内移植的保护作用。 )小鼠在短暂性大脑中动脉闭塞(tMCAO)后在tPA介导的脑损伤中对NVU产生影响。与tMCAO组相比,tMCAO加BMSC组在tMCAO后48小时显示MMP的体内和体外荧光信号显着降低,且BMSC-GFP信号部分共定位。脑内移植的骨髓间充质干细胞通过免疫组织化学和Western印迹改善了MMP-9的活化,并分化为小胶质细胞和星形胶质细胞。双重免疫荧光研究显示tMCAO加BMSC组的NVU破坏得到改善。本研究表明,脑内BMSC移植减少了tMCAO后tPA引起的MMP激活和随后的tPA引起的NVU破坏,并且这种MMP激活和BMSC效应可通过体内和体外光学成像检测到。

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