Tracking of adipose tissue-derived progenitor cells using two magnetic nanoparticle types

被引:6
|
作者
Kasten, Annika [1 ]
Siegmund, Birte J. [1 ]
Gruettner, Cordula [2 ]
Kuehn, Jens-Peter [3 ]
Frerich, Bernhard [1 ]
机构
[1] Univ Rostock, Med Ctr, Dept Oral & Maxillofacial Surg, D-18057 Rostock, Germany
[2] Micromod Partikeltechnol GmbH, D-18115 Rostock, Germany
[3] Ernst Moritz Arndt Univ Greifswald, Med Ctr, Dept Radiol & Neuroradiol, D-17475 Greifswald, Germany
关键词
Iron oxide nanoparticle; Magnetic resonance imaging; Cell tracking; Tissue engineering; Adipose tissue-derived stem cell; MRI;
D O I
10.1016/j.jmmm.2014.08.044
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Magnetic resonance imaging (MRI) is to be considered as an emerging detection technique for cell tracking experiments to evaluate the fate of transplanted progenitor cells and develop successful cell therapies for tissue engineering. Adipose tissue engineering using adipose tissue derived progenitor cells has been advocated for the cure of soft tissue defects or for persistent soft tissue augmentation. Adipose tissue derived progenitor cells were differentiated into the adipogenic lineage and labeled with two different types of magnetic iron oxide nanoparticles in varying concentrations which resulted in a concentration dependent reduction of gene expression of adipogenic differentiation markers, adiponectin and fatty acid binding protein 4 (FABP4), whereas the metabolic activity was not altered. As a result, only low nanoparticle concentrations for labeling were used for in vivo experiments. Cells were seeded onto collagen scaffolds and subcutaneously implanted into severe combined immunodeficient (SCID) mice. At 24 h as well as 28 clays after implantation, MRI analyses were performed visualizing nanoparticle-labeled cells using T2-weighted sequences. The quantification of absolute volume of the scaffolds revealed a decrease of volume over time in all experimental groups. The distribution of nanoparticle-labeled cells within the scaffolds varied likewise over time. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:34 / 38
页数:5
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