Highly efficient endosomal labeling of progenitor and stem cells with large magnetic particles allows magnetic resonance imaging of single cells

Blood. 2003 Aug 1;102(3):867-72. doi: 10.1182/blood-2002-12-3669. Epub 2003 Apr 3.

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.

MeSH terms

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

Substances

  • Antigens, CD34
  • Oxides
  • carboxydextran-coated magnetic iron oxide particles
  • Iron