An Efficient T1 Contrast Agent for Labeling and Tracking Human Embryonic Stem Cells on MRI

Author:

Haedicke Inga E.12,Loai Sadi12,Cheng Hai-Ling Margaret12345ORCID

Affiliation:

1. Institute of Biomaterials & Biomedical Engineering, University of Toronto, 164 College Street, RS407, Toronto, ON, Canada M5S 3G9

2. Ted Rogers Centre for Heart Research, Translational Biology & Engineering Program, Toronto, Canada

3. The Edward S. Rogers Sr. Department of Electrical and Computer Engineering, University of Toronto, Canada

4. Heart & Stroke/Richard Lewar Centre of Excellence for Cardiovascular Research, Toronto, Canada

5. Ontario Institute for Regenerative Medicine, Toronto, Canada

Abstract

Noninvasive cell tracking in vivo has the potential to advance stem cell-based therapies into the clinic. Magnetic resonance imaging (MRI) provides an excellent image-guidance platform; however, existing MR cell labeling agents are fraught with limited specificity. To address this unmet need, we developed a highly efficient manganese porphyrin contrast agent, MnEtP, using a two-step synthesis. In vitro MRI at 3 Tesla on human embryonic stem cells (hESCs) demonstrated high labeling efficiency at a very low dose of 10 µM MnEtP, resulting in a four-fold lower T1 relaxation time. This extraordinarily low dose is ideal for labeling large cell numbers required for large animals and humans. Cell viability and differentiation capacity were unaffected. Cellular manganese quantification corroborated MRI findings, and the agent localized primarily on the cell membrane. In vivo MRI of transplanted hESCs in a rat demonstrated excellent sensitivity and specificity of MnEtP for noninvasive stem cell tracking.

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Hindawi Limited

Subject

Radiology, Nuclear Medicine and imaging

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