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首页> 外文期刊>Brain research >Galectin-1 suppresses methamphetamine induced neuroinflammation in human brain microvascular endothelial cells: Neuroprotective role in maintaining blood brain barrier integrity
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Galectin-1 suppresses methamphetamine induced neuroinflammation in human brain microvascular endothelial cells: Neuroprotective role in maintaining blood brain barrier integrity

机译:Galectin-1抑制人脑微血管内皮细胞中的甲基苯丙胺诱导的神经炎细胞:神经保护作用在维持血脑屏障完整性方面

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摘要

Methamphetamine (Meth) abuse can lead to the breakdown of the blood-brain bather (BBB) integrity leading to compromised CNS function. The role of Galectins in the angiogenesis process in tumor-associated endothelial cells (EC) is well established; however no data are available on the expression of Galectins in normal human brain microvascular endothelial cells and their potential role in maintaining BBB integrity. We evaluated the basal gene/protein expression levels of Galectin-1, -3 and -9 in normal primary human brain microvascular endothelial cells (BMVEC) that constitute the BBB and examined whether Meth altered Galectin expression in these cells, and if Galectin-1 treatment impacted the integrity of an in-vitro BBB. Our results showed that BMVEC expressed significantly higher levels of Galectin-1 as compared to Galectin-3 and -9. Meth treatment increased Galectin-1 expression in BMVEC. Meth induced decrease in TJ proteins ZO-1, Claudin-3 and adhesion molecule ICAM-1 was reversed by Galectin-1. Our data suggests that Galectin-1 is involved in BBB remodeling and can increase levels of TJ proteins ZO-1 and Claudin-3 and adhesion molecule ICAM-1 which helps maintain BBB tightness thus playing a neuroprotective role. Galectin-1 is thus an important regulator of immune balance from neurodegeneration to neuroprotection, which makes it an important therapeutic agent/target in the treatment of drug addiction and other neurological conditions. (C) 2015 Elsevier B.V. All rights reserved.
机译:甲基苯丙胺(甲基)滥用可能导致血脑Bather(BBB)完整性的崩溃,导致CNS功能受损。半抗凝菌素在肿瘤相关内皮细胞(EC)中的血管生成过程中的作用是很好的;然而,在正常人脑微血管内皮细胞中的半乳糖菌素的表达上没有任何数据以及它们在维持BBB完整性方面的作用。我们在构成BBB的正常原发性人脑微血管内皮细胞(BMVEC)中,评估了Galectin-1,-3和-9的基因基因/蛋白表达水平,并检查了这些细胞中的甲基乳蛋白表达是否在这些细胞中的表达,以及Galectin-1治疗影响了体外BBB的完整性。我们的结果表明,与Galectin-3和-9相比,BMVEC表达了Galectin-1水平显着更高。甲基治疗增加了BMVEC中的Galectin-1表达。通过Galectin-1致致乳酪蛋白ZO-1,Claudin-3和粘附分子ICAM-1的致癌致癌致癌。我们的数据表明Galectin-1参与BBB重塑,可以增加TJ蛋白ZO-1和Claudin-3和粘附分子ICAM-1的水平,这有助于维持BBB的紧张,从而起着神经保护作用。因此,Galectin-1是从神经退行到神经保护的一个重要调节因子,这使其成为治疗药物成瘾和其他神经系统的重要治疗剂/靶。 (c)2015 Elsevier B.v.保留所有权利。

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