Cell motility of neural stem cells is reduced after SPIO-labeling, which is mitigated after exocytosis

Magn Reson Med. 2013 Jan;69(1):255-62. doi: 10.1002/mrm.24216. Epub 2012 Feb 28.

Abstract

MRI is used for tracking of superparamagnetic iron oxide (SPIO)-labeled neural stem cells. Studies have shown that long-term MR tracking of rapidly dividing cells underestimates their migration distance. Time-lapse microscopy of random cellular motility and cell division was performed to evaluate the effects of SPIO-labeling on neural stem cell migration. Labeled cells divided symmetrically and exhibited no changes in cell viability, proliferation, or apoptosis. However, SPIO-labeling resulted in decreased motility of neural stem cells as compared with unlabeled controls. When SPIO-labeled neural stem cells and human induced pluripotent stem cells were transplanted into mouse brain, rapid exocytosis of SPIO by live cells was observed as early as 48 h postengraftment, with SPIO-depleted cells showing the farthest migration distance. As label dilution is negligible at this early time point, we conclude that MRI underestimation of cell migration can also occur as a result of reduced cell motility, which appears to be mitigated following SPIO exocytosis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division / drug effects
  • Cell Movement / drug effects*
  • Cells, Cultured
  • Cerebellum / cytology*
  • Contrast Media*
  • Dextrans / pharmacokinetics*
  • Exocytosis / physiology*
  • Magnetite Nanoparticles*
  • Mice
  • Mice, Inbred Strains
  • Neural Stem Cells / metabolism
  • Neural Stem Cells / physiology*
  • Pluripotent Stem Cells / metabolism*
  • Pluripotent Stem Cells / physiology*
  • Stem Cell Transplantation

Substances

  • Contrast Media
  • Dextrans
  • Magnetite Nanoparticles
  • ferumoxtran-10