Effect of Labeling with Iron Oxide Particles or Nanodiamonds on the Functionality of Adipose-Derived Mesenchymal Stem Cells |
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Authors: | Sinead P. Blaber Cameron J. Hill Rebecca A. Webster Jana M. Say Louise J. Brown Shih-Chang Wang Graham Vesey Benjamin Ross Herbert |
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Affiliation: | 1Department of Chemistry and Biomolecular Sciences, Macquarie University, North Ryde, New South Wales, Australia;2Regeneus Ltd, Gordon, New South Wales, Australia;3Department of Physics and Astronomy, Macquarie University, North Ryde, New South Wales, Australia;4Department of Radiology, Westmead Hospital, University of Sydney, Westmead, New South Wales, Australia;University of Medicine and Dentistry of New Jersey, United States of America |
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Abstract: | Stem cells are increasingly the focus of translational research as well as having emerging roles in human cellular therapy. To support these uses there is a need for improved methods for in vivo cell localization and tracking. In this study, we examined the effects of cell labeling on the in vitro functionality of human adipose-derived mesenchymal stem cells. Our results provide a basis for future in vivo studies investigating implanted cell fate and longevity. In particular, we investigated the effects of two different particles: micron-sized (∼0.9 µm) fluorescently labeled (Dragon Green) superparamagnetic iron oxide particles (M-SPIO particles); and, carboxylated nanodiamonds of ∼0.25 µm in size. The effects of labeling on the functionality of adipose-derived MSCs were assessed by in vitro morphology, osteogenic and adipogenic differentiation potential, CD marker expression, cytokine secretion profiling and quantitative proteomics of the intra-cellular proteome. The differentiation and CD marker assays for stem-like functionality were not altered upon label incorporation and no secreted or intra-cellular protein changes indicative of stress or toxicity were detected. These in vitro results indicate that the M-SPIO particles and nanodiamonds investigated in this study are biocompatible with MSCs and therefore would be suitable labels for cell localization and tracking in vivo. |
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