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Functional characterization of mesenchymal stem cells labeled with a novel PVP-coated superparamagnetic iron oxide

Authors
Reddy, Alavala MattaKwak, Byung KookShim, Hyung JinAhn, ChiyoungCho, Sun HangKim, Byung JinJeong, Sang YoungHwang, Sung-JooYuk, Soon Hong
Issue Date
May-2009
Publisher
WILEY-HINDAWI
Keywords
polyvinyl pyrrolidone; superparamagnetic iron oxide; MRI; cell tracking; mesenchymal stem cells
Citation
CONTRAST MEDIA & MOLECULAR IMAGING, v.4, no.3, pp 118 - 126
Pages
9
Journal Title
CONTRAST MEDIA & MOLECULAR IMAGING
Volume
4
Number
3
Start Page
118
End Page
126
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/23208
DOI
10.1002/cmmi.271
ISSN
1555-4309
1555-4317
Abstract
Magnetic resonance imaging of cells labeled with superparamagnetic iron oxide (SPIO) could be a valuable tool for tracking transplanted cells in living organisms. Human bone marrow-derived mesenchymal stem cells (hBMMSC) were labeled with a novel polyvinyl pyrrolidone (PVP)-coated SPIO. Prussian blue staining and electron microscopy revealed that almost all of the cells were efficiently labeled with PVP-SPIO nanoparticles. There were no signs of cytotoxicity, even at concentrations of up to 1600 mu g Fe/ml of the nanoparticles, and the labeled cells were successfully visualized by in vitro cellular MRI. In addition, there was no significant alteration of the phenotype or the adipo/osteo/chondrogenic differentiation potential of the cells. This was in contrast to Feridex IV labeling that led to the inhibition of hBMMSC chondrogenesis. Following intramuscular injection in a rabbit hind limb ischemia model, the intercellular migration of the labeled cells toward the ablated site was clearly tracked through in vivo MRI. The localization of the transplanted cells observed by MRI correlated well with postmortem histological studies. These results demonstrate that the novel PVP-SPIO nanoparticles appear to be efficient MR contrast agents and may enable non-invasive in vivo tracking of stem cells in experimental and clinical settings during cell therapy. Copyright (C) 2009 John Wiley & Sons, Ltd.
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Kwak, Byung Kook
의과대학 (의학부(임상-서울))
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