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Bifunctional Magnetic Silica Nanoparticles for Highly Efficient Human Stem Cell Labeling
Author(s) -
Chen-Wen Lu,
Yann Hung,
JongKai Hsiao,
Ming Yao,
Tsai-Hua Chung,
YuShen Lin,
SiHan Wu,
Szu-Chun Hsu,
HonMan Liu,
ChungYuan Mou,
ChungShi Yang,
Dongming Huang,
YaoChang Chen
Publication year - 2006
Publication title -
nano letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.853
H-Index - 488
eISSN - 1530-6992
pISSN - 1530-6984
DOI - 10.1021/nl0624263
Subject(s) - in vivo , fluorescein isothiocyanate , endocytosis , chemistry , biophysics , iron oxide nanoparticles , intracellular , mesenchymal stem cell , cell , viability assay , in vitro , cell culture , microbiology and biotechnology , nanoparticle , stem cell , nanotechnology , materials science , biochemistry , biology , fluorescence , physics , genetics , quantum mechanics
A superparamagnetic iron oxide (SPIO) nanoparticle is emerging as an ideal probe for noninvasive cell tracking. However, its low intracellular labeling efficiency has limited the potential usage and has evoked great interest in developing new labeling strategies. We have developed fluorescein isothiocyanate (FITC)-incorporated silica-coated core-shell SPIO nanoparticles, SPIO@SiO2(FITC), with diameters of 50 nm, as a bifunctionally magnetic vector that can efficiently label human mesenchymal stem cells (hMSCs), via clathrin- and actin-dependent endocytosis with subsequent intracellular localization in late endosomes/lysosomes. The uptake process displays a time- and dose-dependent behavior. In our system, SPIO@SiO2(FITC) nanoparticles induce sufficient cell MRI contrast at an incubation dosage as low as 0.5 microg of iron/mL of culture medium with 1.2x105 hMSCs, and the in vitro detection threshold of cell number is about 1x104 cells. Furthermore, 1.2x105 labeled cells can also be MRI-detected in a subcutaneous model in vivo. Labeled hMSCs are unaffected in their viability, proliferation, and differentiation capacities into adipocytes and osteocytes which can still be readily MRI detected. This is the first report that hMSCs can be efficiently labeled with MRI contrast nanoparticles and can be monitored in vitro and in vivo with a clinical 1.5-T MRI imager under low incubation concentration of iron oxide, short incubation time, and low detection cell numbers at the same time.

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