A liposomal system for contrast-enhanced magnetic resonance imaging of molecular targets

被引:189
作者
Mulder, WJM
Strijkers, GJ
Griffioen, AW
van Bloois, L
Molema, G
Storm, G
Koning, GA
Nicolay, K
机构
[1] Eindhoven Univ Technol, Dept Biomed Engn, Biomed NMR, NL-5600 MB Eindhoven, Netherlands
[2] Maastricht Univ & Univ Hosp, Angiogenesis Lab, Dept Pathol Internal Med, NL-6225 EH Maastricht, Netherlands
[3] Utrecht Inst Pharmaceut Sci, Dept Pharmaceut, NL-3508 TB Utrecht, Netherlands
[4] Univ Groningen, Dept Pathol & Lab Med, Med Biol Sect, NL-9700 RB Groningen, Netherlands
[5] Delft Univ Technol, Interfac Reactor Inst, NL-2629 JB Delft, Netherlands
关键词
D O I
10.1021/bc049949r
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Pegylated paramagnetic and fluorescent immunoliposomes were designed to enable the parallel detection of the induced expression of molecular markers on endothelial cells with magnetic resonance imaging (MRI) and fluorescence microscopy. MRI is capable of three-dimensional noninvasive imaging of opaque tissues at near cellular resolution, while fluorescence microscopy can be used to investigate processes at the subcellular level. As a model for the expression of a molecular marker, human umbilical vein endothelial cells (HUVEC) were treated with the pro-inflammatory cytokine tumor necrosis factor alpha (TNFalpha) to upregulate the expression of the adhesion molecule E-selectin/CD62E. E-selectin-expressing HUVEC were incubated with pegylated paramagnetic fluorescently labeled liposomes carrying anti-E-selectin monoclonal antibody as a targeting ligand. Both MRI and fluorescence microscopy revealed the specific association of the liposomal MR contrast agent with stimulated HUVEC. This study suggests that this newly developed system may serve as a useful diagnostic tool to investigate pathological processes in vivo with MRI.
引用
收藏
页码:799 / 806
页数:8
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