4.4 Article

Superparamagnetic iron oxide does not affect the viability and function of adipose-derived stem cells, and superparamagnetic iron oxide-enhanced magnetic resonance imaging identifies viable cells

Journal

MAGNETIC RESONANCE IMAGING
Volume 27, Issue 1, Pages 108-119

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.mri.2008.05.013

Keywords

Adipose-derived stem cells; Magnetic resonance imaging; Superparamagnetic iron oxide; Transdifferentiation; Viability

Funding

  1. National Research Council Canada
  2. Canadian Institutes of Health Research
  3. Cardiac Sciences Program of St. Boniface General Hospital

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The objectives of this study were (1) to determine whether superparamagnetic iron oxide (SPIO) affects viability, transdifferentiation potential and cell-factor secretion of adipose-derived stein cells (ASCs); and (2) to determine whether SPIO-enhanced magnetic resonance (MR) imaging highlights living stein cells. Rat ASCs were incubated in SPIO-containing cell culture medium for 2 days. The SPIO-treated ASCs were then subjected to adipogenic, osteogenic and myogenic transdifferentiation. Expression of vascular endothelial growth factor, hepatocyte growth factor and insulin-like growth factor I by the SPIO-treated ASCs was measured using reverse transcription polymerase chain reaction. Cell viability was assessed using trypan blue stain. For in vivo experiments, SPIO-labeled ASCs were injected into 10 rat hearts. The hearts were monitored using, MRI. We found that Survival rate of the ASCs Cultured in the SPIO-containing medium was very high (97-99%). The SPIO-treated ASCs continued to express specific markers for the three types of transdifferentiation. Expression of the cell factors by the ASCs was not affected by SPIO. Signal voids on MR images were associated with the living SPIO-labeled ASCs in the rat hearts. We Conclude that SPIO does not affect viability, transdifferentiation potential or cell-factor secretion of ASCs. MRJ mainly highlights living SPIO-labeled stem cells. Crown Copyright (C) 2009 Published by Elsevier Inc. All rights reserved.

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