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首页> 外文期刊>Journal of Molecular Neuroscience: MN >The role of caveolin-1 in blood-brain barrier disruption induced by focused ultrasound combined with microbubbles
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The role of caveolin-1 in blood-brain barrier disruption induced by focused ultrasound combined with microbubbles

机译:小窝蛋白1在聚焦超声与微泡结合引起的血脑屏障破坏中的作用

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This research was designed to determine whether disrupting the blood-brain barrier (BBB) in rats by applying focused ultrasound (FUS) combined with micro-bubbles induced changes in the density of caveolae and/or the expression of the structural protein caveolin-1. To this end, two approaches were utilized. First, using enhanced magnetic resonance imaging, characteristics of BBB disruption induced by our specific FUS parameters and dose of microbubble were recorded, and the time after treatment when the BBB was the most permeable was determined. Second, rats were treated with FUS or microbubbles alone, both or neither, and a combination of Evans blue (EB) BBB permeability assays, streptavidin-peroxidase (SP) immunohistochemistry, western blot, and transmission electron microscopy (TEM) was employed to detect any changes in caveolae density and caveolin-1 expression at the previously determined time point when the BBB was the most permeable. The first set of studies revealed that our specific FUS parameters and dose of microbubbles were able to induce a transient, targeted, and reversible BBB opening in rats, and that the BBB was the most permeable 1 h after treatment with FUS and microbubbles. In the second set of experiments, the results of the SP immuno-histochemistry, western blot, and TEM, taken together, revealed that caveolae and caveolin-1 were primarily localized in the brain microvascular endothelial cells of all of the rats regardless of treatment, and that caveolin-1 expression was highest in the rats treated with both FUS and microbubbles. In summary, treatment with FUS, in combination with a dose of microbubbles, can enhance BBB permeability through a caveolae-mediated transcellular approach by upregulating the expression level of caveolin-1 and, consequently, the amount of caveolae. This caveolin-1-mediated transcellular transport pathway may cooperate with other transport pathways to induce opening of the BBB. This research sheds light on the mechanism of a transient, targeted, and reversible opening of the BBB induced by FUS combined with microbubbles.
机译:这项研究旨在确定是否通过应用聚焦超声(FUS)与微泡相结合来破坏大鼠的血脑屏障(BBB),从而引起小窝密度的改变和/或结构蛋白小窝蛋白1的表达。为此,采用了两种方法。首先,使用增强的磁共振成像,记录由我们的特定FUS参数和微泡剂量引起的BBB破坏特征,并确定治疗后BBB最易渗透的时间。其次,仅对大鼠进行FUS或微泡治疗,或两者都不进行,或者采用伊文思蓝(EB)BBB渗透性测定,链霉亲和素过氧化物酶(SP)免疫组织化学,免疫印迹和透射电镜(TEM)进行检测在先前确定的BBB最易渗透的时间点,小窝密度和小窝蛋白1表达发生任何变化。第一组研究表明,我们特定的FUS参数和微泡剂量能够诱导大鼠短暂,有针对性和可逆的BBB开放,并且在用FUS和微泡处理1小时后,BBB的渗透性最高。在第二组实验中,SP免疫组织化学,Western印迹和TEM的结果共同显示,无论治疗如何,caveolae和Caveolin-1主要位于所有大鼠的大脑微血管内皮细胞中,在FUS和微泡处理的大鼠中,caveolin-1的表达最高。总之,用FUS结合一定剂量的微泡处理,可以通过上调小窝蛋白1的表达水平,进而上调小窝蛋白的量,通过小窝蛋白介导的跨细胞途径增强BBB的通透性。该caveolin-1介导的跨细胞转运途径可能与其他转运途径协同作用,以诱导血脑屏障的开放。这项研究揭示了FUS结合微泡诱导BBB短暂,有针对性和可逆打开的机制。

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