Abstract

Background. Regenerative therapy is an emerging treatment modality. To determine migration and retention of implanted cells, it is crucial to develop noninvasive tracking methods. The aim was to determine ex vivo magnetic resonance imaging (MRI) detection limits of ultrasmall superparamagnetic iron-oxide (USPIO) labeled mesenchymal stromal cells (MSCs). Materials and Methods. 248 gel-phantoms were constructed and scanned on a 1.5T MRI-scanner. Phantoms contained human MSCs preincubated with USPIO nanoparticles for 2, 6, or 21 hours using 5 or 10 μg USPIO/105 MSCs. In addition, porcine hearts were scanned after injection of USPIO labeled MSCs. Results. Using 21 h incubation time and 10 μg USPIO/105 MSCs, labeled cells were clearly separated from unlabeled cells on MRI using 250.000 (P < 0.001), 500.000 (P = 0.007), and 1.000.000 MSCs (P = 0.008). At lower incubation times and doses, neither labeled nor unlabeled cells could be separated. In porcine hearts labeled, but not unlabeled, MSCs were identified on MRI. Conclusions. As few as 250.000 MSCs can be detected on MRI using 21 h incubation time and 10 μg USPIO/105 MSCs. At lower incubation times and doses, several million cells are needed for MRI detection. USPIO labeled cells can be visualized by MRI in porcine myocardial tissue.

Highlights

  • Stem cell therapy with potential to regenerate damaged myocardium is an emerging treatment modality for ischemic heart disease [1,2,3]

  • Determination of the cellular iron load showed a positive correlation between iron content per cell and the length of the ultrasmall superparamagnetic iron-oxide (USPIO) incubation period

  • The cells labeled for 21 hours with the full USPIO dose had significantly higher iron content than the cells labeled for 21 hours with only half USPIO dose

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Summary

Introduction

Stem cell therapy with potential to regenerate damaged myocardium is an emerging treatment modality for ischemic heart disease [1,2,3]. For future success of cardiac stem cell therapy, it is crucial to develop noninvasive tracking methods for determining the biodistribution and fate of the stem cells after delivery. Providing highly sensitive visualization, these methods are limited by low spatial resolution and short half-lives of radioisotopes from minutes to hours, only permitting short-term tracking of the cells. Tracking of cells labeled with superparamagnetic ironoxide (SPIO) or ultrasmall superparamagnetic iron-oxide (USPIO) nanoparticles using magnetic resonance imaging (MRI) offers high spatial resolution in combination with high. The aim was to determine ex vivo magnetic resonance imaging (MRI) detection limits of ultrasmall superparamagnetic iron-oxide (USPIO) labeled mesenchymal stromal cells (MSCs). Using 21 h incubation time and 10 μg USPIO/105 MSCs, labeled cells were clearly separated from unlabeled cells on MRI using 250.000 (P < 0.001), 500.000 (P = 0.007), and 1.000.000 MSCs (P = 0.008). USPIO labeled cells can be visualized by MRI in porcine myocardial tissue

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