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Blood ; 102(3): 867-72, 2003 Aug 01.
Article in English | MEDLINE | ID: mdl-12676779

ABSTRACT

Tracking transplanted stem cells using magnetic resonance imaging (MRI) could offer biologic insight into homing and engraftment. Ultrasmall dextran-coated iron oxide particles have previously been developed for uptake into cells to allow MRI tracking. We describe a new application of much larger, micron-scale, iron oxide magnetic particles with enhanced MR susceptibility, which enables detection of single cells at resolutions that can be achieved in vivo. In addition, these larger particles possess a fluorophore for histologic confirmation of cell distribution. We demonstrate highly efficient, nontoxic, endosomal uptake of these particles into hematopoietic CD34+ cells and mesenchymal stem cells documented by confocal and electron microscopy. Labeled cells retain biologic activity with preservation of colony-forming ability and differentiation capacity. MRI studies could detect labeled CD34+ cells and mesenchymal stem cells (MSCs) at single cell resolution. This appears to be a promising tool for serial noninvasive monitoring of in vivo cell homing and localization using MRI.


Subject(s)
Endosomes/metabolism , Iron/pharmacokinetics , Magnetic Resonance Imaging/methods , Oxides/pharmacokinetics , Stem Cells/metabolism , Animals , Antigens, CD34 , Cell Differentiation , Cell Division , Hematopoietic Stem Cells/cytology , Hematopoietic Stem Cells/metabolism , Humans , Mesoderm/cytology , Microscopy, Confocal , Microscopy, Electron , Osteogenesis , Pluripotent Stem Cells/cytology , Pluripotent Stem Cells/metabolism , Stem Cells/cytology , Swine
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