Thromb Haemost 2005; 93(05): 910-913
DOI: 10.1160/TH04-10-0660
Platelets and Blood Cells
Schattauer GmbH

Non-invasive imaging of glycoprotein VI binding to injured arterial lesions

Meinrad Gawaz
1   Medizinische Klink III, Universitätsklinikum Tübingen, Tübingen, Germany
,
Ildiko Konrad
2   Medizinische Klinik und Poliklinik, Technische Universität München, Munich, Germany
,
Andrea I. Hauser
3   Nuklearmedizinische Klinik, Klinikum rechts der Isar, Technische Universität München, Munich, Germany
,
Suzanne Sauer
1   Medizinische Klink III, Universitätsklinikum Tübingen, Tübingen, Germany
,
Zhongyan Li
1   Medizinische Klink III, Universitätsklinikum Tübingen, Tübingen, Germany
,
Hans-Jürgen Wester
3   Nuklearmedizinische Klinik, Klinikum rechts der Isar, Technische Universität München, Munich, Germany
,
Frank M. Bengel
3   Nuklearmedizinische Klinik, Klinikum rechts der Isar, Technische Universität München, Munich, Germany
,
Markus Schwaiger
3   Nuklearmedizinische Klinik, Klinikum rechts der Isar, Technische Universität München, Munich, Germany
,
Albert Schömig
2   Medizinische Klinik und Poliklinik, Technische Universität München, Munich, Germany
,
Steffen Massberg
1   Medizinische Klink III, Universitätsklinikum Tübingen, Tübingen, Germany
,
Roland Haubner
3   Nuklearmedizinische Klinik, Klinikum rechts der Isar, Technische Universität München, Munich, Germany
4   Universitätsklinik für Nuklearmedizin, Medizinische Universität Innsbruck, Austria
› Author Affiliations

Financial support: The study was supported in part by grants from the Deutsche Forschungsgemeinschaft (Graduiertenkolleg 483) and the Wilhelm-Sander Stiftung.
Further Information

Publication History

Received 11 October 2004

Accepted after revision 04 February 2005

Publication Date:
11 December 2017 (online)

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Summary

Glycoprotein VI (GPVI) is the major platelet collagen receptor and plays a critical role in the process of thrombosis at sites of atherosclerotic lesions. This study evaluates the feasibility of radiolabeled soluble GPVI to identify injured arterial lesions. Radiolabeling was carried out using the iodogen method and resulted in the radioiodinated GPVI in radiochemical yields between 97–100%. The biodistribution of [125I]GPVI was determined in normal mice and demonstrated a blood clearance halftime of approximately 5.5 hours. Vascular lesions were induced in the carotid artery in wild type and ApoE -/- mice. Immediately after injury radioiodinated GPVI was injected intravenously. Binding of [123I]GPVI to carotid lesions was assessed by szinti-graphic in vivo imaging. Carotid arteries were explanted for ex vivo autoradiography and histological characterization of the lesion. In vivo and ex vivo imaging revealed substantial accumulation of radioiodinated GPVI in the injured artery wall, with a ratio of lesion to control vessel of 3:1 and 7:1, respectively. Because GPVI is the critical collagen receptor that mediates platelet adhesion to vascular lesions, soluble radiolabeled GPVI may be an agent for non-invasive imaging of thrombogenic thus, vulnerable atherosclerotic plaques.