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Cardiovascular Research Advance Access [Accepted Manuscript] published online on June 29, 2009

Cardiovascular Research, doi:10.1093/cvr/cvp218
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Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2009. For permissions please email: journals.permissions@oxfordjournals.org.

MOLECULAR IMAGING OF ENDOTHELIAL PROGENITOR CELL ENGRAFTMENT USING CONTRAST-ENHANCED ULTRASOUND AND TARGETED MICROBUBBLES

Michael A. Kuliszewski, BSc.1, Hiroko Fujii, M.D., PhD.1, Christine Liao, BSc.1, Alexandra H. Smith, BSc.1, Aris Xie, MSc.2, Jonathan R. Lindner, M.D.2 and Howard Leong-Poi, M.D.1

1 From the Division of Cardiology, Keenan Research Centre in the Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada
2 The Cardiovascular Division, Oregon Health & Science University, Portland, Oregon

Address correspondence to: Howard Leong-Poi M.D., 7-052 Bond Wing, St. Michael's Hospital, 30 Bond Street, Toronto, Ontario, Canada M5B 1W8, Tel: (416) 864-5201, FAX: (416) 864-5571, E-mail: leong-poih{at}smh.toronto.on.ca

Aims: Imaging methods to track the fate of progenitor cells after their delivery would be useful in assessing the efficacy of cell-based therapies. We hypothesized that contrast-enhanced ultrasound (CEU) using microbubbles targeted to a genetically engineered cell-surface marker on endothelial progenitor cells (EPCs) would allow the targeted imaging of vascular engraftment.

Methods: Rodent bone-marrow derived EPCs were isolated, cultured, and transfected to express the marker protein, H-2Kk, on the cell surface. Non-transfected EPCs and EPCs transfected with either null plasmid or firefly luciferase served as controls. Control microbubbles (MBC) and microbubbles targeted to H-2Kk expressed on EPCs (MBH2Kk) were constructed. Binding of targeted microbubbles to EPCs was assessed in vitro using a parallel plate flow chamber system. CEU imaging of EPC-targeted microbubbles was assessed in vivo using subcutaneously implanted EPC-supplemented matrigel plugs in rats.

Results: In flow chamber experiments, there was minimal attachment of microbubbles to plated control EPCs. While numbers of adhered MBC were also low, there was greater and more diffuse attachment of MBH2Kk to plated H-2Kk transfected EPCs. Targeted CEU demonstrated marked contrast enhancement at the periphery of the H-2Kk-transfected EPC-supplemented matrigel plug for MBH2Kk whereas contrast enhancement was low for MBC. Contrast enhancement was also low for both microbubbles within control mock-transfected EPC plugs. The signal intensity within the H-2Kk-transfected EPC plug was significantly greater for MBH2Kk as compared to MBC.

Conclusions: Microbubbles targeted to a genetically engineered cell-surface marker on EPCs exhibit specific binding to EPCs in vitro. These targeted microbubbles bind to engrafted EPCs in vivo within matrigel plugs, and can be detected by their enhancement on CEU imaging.


Time for primary review: 28 Days


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H. Leong-Poi
Molecular imaging using contrast-enhanced ultrasound: evaluation of angiogenesis and cell therapy
Cardiovasc Res, November 1, 2009; 84(2): 190 - 200.
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