Document Detail

In vivo quantitative assessment of cell viability of gadolinium or iron-labeled cells using MRI and bioluminescence imaging.
MedLine Citation:
PMID:  23281289     Owner:  NLM     Status:  In-Data-Review    
In cell therapy, noninvasive monitoring of in vivo cell fate is challenging. In this study we investigated possible differences in R(1) , R(2) or R(2) * relaxation rate as a measure of overall cell viability for mesenchymal stem cells labeled with Gd-liposomes (Gd-MSCs) or iron oxide nanoparticles (SPIO-MSCs). Cells were also transduced with a luciferase vector, facilitating a correlation between MRI findings and cell viability using bioluminescence imaging (BLI). Viable Gd-MSCs were clearly distinguishable from nonviable Gd-MSCs under both in vitro and in vivo conditions, clearly differing quantitatively (ΔR(1) and ΔR(2) ) as well as by visual appearance (hypo- or hyperintense contrast). Immediately post-injection,viable Gd-MSCs caused a substantially larger ΔR(2) and lower ΔR(1) effect compared with nonviable MSCs. With time, the ΔR(1) and ΔR(2) relaxation rate showed a good negative correlation with increasing cell number following proliferation. Upon injection, no substantial quantitative or visual differences between viable and nonviable SPIO-MSCs were detected. Moreover, nonviable SPIO-MSCs caused a persisting signal void in vivo, compromising the specificity of this contrast agent. In vivo persistence of SPIO particles was confirmed by histological staining. A large difference was found between SPIO- and Gd-labeled cells in the accuracy of MR relaxometry in assessing the cell viability status. Gd-liposomes provide a more accurate and specific assessment of cell viability than SPIO particles. Viable Gd cells can be differentiated from nonviable Gd cells even by visual interpretation. These findings clearly indicate Gd to be the favourable contrast agent in qualitative and quantitative evaluation of labeled cell fate in future cell therapy experiments. Copyright © 2012 John Wiley & Sons, Ltd.
Jamal Guenoun; Alessandro Ruggiero; Gabriela Doeswijk; Roel C Janssens; Gerben A Koning; Gyula Kotek; Gabriel P Krestin; Monique R Bernsen
Related Documents :
24035389 - Nkx6.1 is essential for maintaining the functional state of pancreatic beta cells.
23994259 - Shades of grey: the delineation of marker expression within the adult rodent subventric...
24202489 - Cell-cell interactions in the testis of the dogfish: stage-related changes in protein s...
23352099 - Exogenous administration of recombinant human fsh does not improve germ cell survival i...
22961649 - Platelet-derived growth factor promotes the proliferation of human umbilical cord-deriv...
23571709 - The role of ovarian surface epithelium in folliculogenesis during fetal development of ...
24035389 - Nkx6.1 is essential for maintaining the functional state of pancreatic beta cells.
9076939 - Myofibroblasts and local angiotensin ii in rat cardiac tissue repair.
9744879 - A morphogenesis checkpoint monitors the actin cytoskeleton in yeast.
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Contrast media & molecular imaging     Volume:  8     ISSN:  1555-4317     ISO Abbreviation:  Contrast Media Mol Imaging     Publication Date:  2013 Mar 
Date Detail:
Created Date:  2013-01-02     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101286760     Medline TA:  Contrast Media Mol Imaging     Country:  United States    
Other Details:
Languages:  eng     Pagination:  165-74     Citation Subset:  IM    
Copyright Information:
Copyright © 2012 John Wiley & Sons, Ltd.
Department of Radiology, Erasmus MC - University Medical Center Rotterdam, Rotterdam, The Netherlands.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Detection of vascular cell adhesion molecule-1 expression with USPIO-enhanced molecular MRI in a mou...
Next Document:  Synthesis and in vitro evaluation of MR molecular imaging probes using J591 mAb-conjugated SPIONs fo...