Tysiak Eva, Asbach Patrick, Aktas Orhan, Waiczies Helmar, Smyth Maureen, Schnorr Joerg, Taupitz Matthias, Wuerfel Jens
Cecilie Vogt Clinic for Neurology, Charité - University Medicine Berlin, Germany.
J Neuroinflammation. 2009 Aug 6;6:20. doi: 10.1186/1742-2094-6-20.
BACKGROUND: Gadopentate dimeglumine (Gd-DTPA) enhanced magnetic resonance imaging (MRI) is widely applied for the visualization of blood brain barrier (BBB) breakdown in multiple sclerosis and its animal model, experimental autoimmune encephalomyelitis (EAE). Recently, the potential of magnetic nanoparticles to detect macrophage infiltration by MRI was demonstrated. We here investigated a new class of very small superparamagnetic iron oxide particles (VSOP) as novel contrast medium in murine adoptive-transfer EAE. METHODS: EAE was induced in 17 mice via transfer of proteolipid protein specific T cells. MR images were obtained before and after application of Gd-DTPA and VSOP on a 7 Tesla rodent MR scanner. The enhancement pattern of the two contrast agents was compared, and correlated to histology, including Prussian Blue staining for VSOP detection and immunofluorescent staining against IBA-1 to identify macrophages/microglia. RESULTS: Both contrast media depicted BBB breakdown in 42 lesions, although differing in plaques appearances and shapes. Furthermore, 13 lesions could be exclusively visualized by VSOP. In the subsequent histological analysis, VSOP was localized to microglia/macrophages, and also diffusely dispersed within the extracellular matrix. CONCLUSION: VSOP showed a higher sensitivity in detecting BBB alterations compared to Gd-DTPA enhanced MRI, providing complementary information of macrophage/microglia activity in inflammatory plaques that has not been visualized by conventional means.
背景:钆喷酸葡胺(Gd-DTPA)增强磁共振成像(MRI)广泛应用于多发性硬化及其动物模型实验性自身免疫性脑脊髓炎(EAE)中血脑屏障(BBB)破坏的可视化。最近,已证实磁性纳米颗粒通过MRI检测巨噬细胞浸润的潜力。我们在此研究了一类新型的超小超顺磁性氧化铁颗粒(VSOP)作为小鼠过继转移EAE中的新型造影剂。 方法:通过转移蛋白脂蛋白特异性T细胞在17只小鼠中诱导EAE。在7特斯拉啮齿动物MR扫描仪上,在应用Gd-DTPA和VSOP之前和之后获取MR图像。比较了两种造影剂的增强模式,并与组织学相关联,包括用于VSOP检测的普鲁士蓝染色和针对IBA-1的免疫荧光染色以识别巨噬细胞/小胶质细胞。 结果:两种造影剂均在42个病变中显示出BBB破坏,尽管斑块外观和形状不同。此外,13个病变只能通过VSOP可视化。在随后的组织学分析中,VSOP定位于小胶质细胞/巨噬细胞,并且也弥漫性地分散在细胞外基质中。 结论:与Gd-DTPA增强MRI相比,VSOP在检测BBB改变方面显示出更高的灵敏度,提供了炎症斑块中巨噬细胞/小胶质细胞活性的补充信息,而这些信息是传统方法无法可视化的。
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