MRI Tracking of Macrophages Labeled with Glucan Particles Entrapping a Water Insoluble Paramagnetic Gd-Based Agent

被引:17
作者
Figueiredo, Sara [1 ,2 ,3 ,6 ,7 ]
Carlos Cutrin, Juan [1 ,2 ,3 ,4 ]
Rizzitelli, Silvia [1 ,2 ,3 ]
De Luca, Elisa [1 ,2 ,3 ]
Moreira, Joao Nuno [5 ,7 ]
Geraldes, Carlos F. G. C. [6 ,7 ,8 ]
Aime, Silvio [1 ,2 ,3 ]
Terreno, Enzo [1 ,2 ,3 ]
机构
[1] Univ Turin, Dept Mol Biotechnol, Turin, Italy
[2] Univ Turin, Hlth Sci Ctr, Turin, Italy
[3] Univ Turin, Mol & Preclin Imaging Ctr, Turin, Italy
[4] ININCA UBA CONICET, Buenos Aires, DF, Argentina
[5] Univ Coimbra, FFUC Fac Pharm, Coimbra, Portugal
[6] Univ Coimbra, Fac Sci & Technol, Dept Life Sci, Coimbra, Portugal
[7] Univ Coimbra, CNC Ctr Neurosci & Cell Biol, Coimbra, Portugal
[8] Univ Coimbra, Coimbra Chem Ctr, Coimbra, Portugal
关键词
MRI; Gadolinium; Paramagnetic MRI agents; Glucan particles; Cell tracking; OXIDE NANOPARTICLES; DENDRITIC CELLS; BETA-GLUCANS; STEM-CELLS; IN-VITRO; IMMUNE; DELIVERY; RECEPTOR; DECTIN-1; MACROPINOCYTOSIS;
D O I
10.1007/s11307-012-0603-x
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
This study is aimed at demonstrating the in vivo potential of Gd(III)-loaded glucan particles (Gd-GPs) as magnetic resonance imaging (MRI)-positive agents for labeling and tracking phagocytic cells. GPs were obtained from Saccharomyces cerevisae and loaded with the water-insoluble complex Gd-DOTAMA(C-18)(2). The uptake kinetics of Gd-GPs by murine macrophages was studied in vitro and the internalization mechanism was assessed by competition assays. The in vivo performance of Gd-GPs was tested at 7.05 T on a mouse model of acute liver inflammation. The minimum number of Gd-GPs-labeled J774.A1 macrophages detected in vitro by MRI was ca. 300 cells/mu l of agar, which is the lowest number ever reported for cells labeled with a positive T-1 agent. Intravenous injection of macrophages labeled with Gd-GPs in a mouse model of liver inflammation enabled the MRI visualization of the cellular infiltration in the diseased area. Gd-GPs represent a promising platform for tracking macrophages by MRI as a T-1 alternative to the golden standard T-2-based iron oxide particles.
引用
收藏
页码:307 / 315
页数:9
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