Improved route for the visualization of stem cells labeled with a Gd-/Eu-chelate as dual (MRI and fluorescence) agent

被引:133
作者
Crich, SG
Biancone, L
Cantaluppi, V
Esposito, DDG
Russo, S
Camussi, G
Aime, S
机构
[1] Univ Turin, IFM, Dept Chem, I-10125 Turin, Italy
[2] Univ Turin, Ctr Mol Imaging, Turin, Italy
[3] Univ Turin, Res Ctr Expt Med, CeRMS, Turin, Italy
[4] Univ Turin, CeRMS, Dept Internal Med, Turin, Italy
关键词
endothelial progenitor cells; magnetic resonance; imaging; cell labeling; Gd/Eu-complexes; fluorescence microscopy;
D O I
10.1002/mrm.20072
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
A simple labeling procedure of stem/progenitor cells based on the use of Gd-HPDO3A and Eu-HPDO3A, respectively, is described. The Gd-chelate acts as T-1-agent for MRI visualization, whereas the corresponding Eu-chelate acts as reporter in fluorescence microscopy. Owing to their substantial chemical equivalence, the two chelates are equally internalized in EPCs (endothelial progenitor cells), thus allowing their visualization by both techniques. The lanthanide chelates are entrapped in endosomic vesicles and the labeled cells retain biological activity with preservation of viability and pro-angiogenesis capacity. Hyperintense spots in MR have been observed for Gd-labeled EPCs injected under mice kidney capsule or grafted on a subcutaneous Matrigel plug up to 14 days after transplantation. Magn Reson Med 51:938-944, 2004. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:938 / 944
页数:7
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