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Monitoring transplanted human mesenchymal stem cells in rat and rabbit bladders using molecular magnetic resonance imaging
Author(s) -
Song Yun Seob,
Ku Ja Hyeon
Publication year - 2007
Publication title -
neurourology and urodynamics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 90
eISSN - 1520-6777
pISSN - 0733-2467
DOI - 10.1002/nau.20351
Subject(s) - mesenchymal stem cell , magnetic resonance imaging , in vivo , medicine , pathology , staining , rabbit (cipher) , stem cell , anatomy , nuclear medicine , radiology , biology , microbiology and biotechnology , statistics , mathematics
Aims This study investigated whether superparamagnetic iron oxide (SPIO)‐labeled human mesenchymal stem cells (hMSCs) may be monitored non‐invasively by in vivo magnetic resonance (MR) imaging with conventional 1.5‐T system examinations in the bladders of rats and rabbits. Methods SPIO were transferred to hMSCs, using GenePORTER. After SPIO‐labeled hMSCs were transplanted into the animal bladders, serial T2‐weighted MR images and histological examinations were performed over a 4‐week period. Results hMSCs loaded with SPIO, compared to unlabeled cells, showed similar viability. SPIO‐labeled hMSCs underwent normal chondrogenic, adipogenic, and osteogenic differentiation. For SPIO‐labeled hMSCs concentrations that were greater than 1 × 10 5 , in vitro MR images showed a decrease in signal intensity. MR signal intensity at the areas of SPIO‐labeled hMSCs in rat and rabbit bladders were decreased and confined locally. After injection of SPIO‐labeled hMSCs into the bladder, MR imaging demonstrated that hMSCs could be seen for at least 12 weeks post‐injection. The presence of iron was confirmed with Prussian blue staining in histological sections. Conclusions Our findings suggest that hMSCs in animal bladders can be monitored non‐invasively with conventional MR imaging. Neurourol. Urodynam. 26:584–593, 2007. © 2007 Wiley‐Liss, Inc.