Molecular imaging of MMP activity discriminates unstable from stable plaque phenotypes in shear-stress induced murine atherosclerosis
PURPOSE: As atherosclerotic plaque ruptures are the primary cause of ischaemic events, their preventive identification by imaging remains a clinical challenge. Matrix metalloproteinases (MMP) are involved in plaque progression and destabilisation and are therefore promising targets to characterize r...
Authors: | |
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Division/Institute: | FB 05: Medizinische Fakultät |
Document types: | Article |
Media types: | Text |
Publication date: | 2018 |
Date of publication on miami: | 28.05.2019 |
Modification date: | 28.11.2023 |
Edition statement: | [Electronic ed.] |
Source: | PLoS ONE 13 (2018) 10, e0204305, 1-16 |
DDC Subject: | 610: Medizin und Gesundheit |
License: | CC BY 4.0 |
Language: | English |
Funding: | Finanziert durch den Open-Access-Publikationsfonds 2018 der Deutschen Forschungsgemeinschaft (DFG) und der Westfälischen Wilhelms-Universität Münster (WWU Münster). |
Format: | PDF document |
URN: | urn:nbn:de:hbz:6-64189621633 |
Other Identifiers: | DOI: 10.1371/journal.pone.0204305 |
Permalink: | https://nbn-resolving.de/urn:nbn:de:hbz:6-64189621633 |
Digital documents: | artikel_seifert_2018.pdf |
PURPOSE: As atherosclerotic plaque ruptures are the primary cause of ischaemic events, their preventive identification by imaging remains a clinical challenge. Matrix metalloproteinases (MMP) are involved in plaque progression and destabilisation and are therefore promising targets to characterize rupture-prone unstable plaques. This study aims at evaluating MMP imaging to discriminate unstable from stable plaque phenotypes. METHODS: ApoE deficient mice (ApoE-/-) on a high cholesterol diet underwent implantation of a tapered cuff around the right common carotid artery (CCA) inducing a highly inflamed atherosclerotic plaque upstream (US) and a more stable plaque phenotype downstream (DS) of the cuff. 8 weeks after surgery, the MMP inhibitor-based photoprobe Cy5.5-AF443 was administered i.v. 3h prior to in situ and ex vivo fluorescence reflectance imaging of the CCAs. Thereafter, CCAs were analysed regarding plaque size, presence of macrophages, and MMP-2 and MMP-9 concentrations by immunohistochemistry and ELISA. RESULTS: We found a significantly higher uptake of Cy5.5-AF443 in US as compared to DS plaques in situ (1.29 vs. 1.06 plaque-to-background ratio; p