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Imaging of Dysfunctional Elastogenesis in Atherosclerosis Using an Improved Gadolinium-Based Tetrameric MRI Probe Targeted to Tropoelastin
[Image: see text] Dysfunctional elastin turnover plays a major role in the progression of atherosclerotic plaques. Failure of tropoelastin cross-linking into mature elastin leads to the accumulation of tropoelastin within the growing plaque, increasing its instability. Here we present Gd(4)-TESMA, a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558862/ https://www.ncbi.nlm.nih.gov/pubmed/34661390 http://dx.doi.org/10.1021/acs.jmedchem.1c01286 |
Sumario: | [Image: see text] Dysfunctional elastin turnover plays a major role in the progression of atherosclerotic plaques. Failure of tropoelastin cross-linking into mature elastin leads to the accumulation of tropoelastin within the growing plaque, increasing its instability. Here we present Gd(4)-TESMA, an MRI contrast agent specifically designed for molecular imaging of tropoelastin within plaques. Gd(4)-TESMA is a tetrameric probe composed of a tropoelastin-binding peptide (the VVGS-peptide) conjugated with four Gd(III)-DOTA-monoamide chelates. It shows a relaxivity per molecule of 34.0 ± 0.8 mM(–1) s(–1) (20 MHz, 298 K, pH 7.2), a good binding affinity to tropoelastin (K(D) = 41 ± 12 μM), and a serum half-life longer than 2 h. Gd(4)-TESMA accumulates specifically in atherosclerotic plaques in the ApoE(–/–) murine model of plaque progression, with 2 h persistence of contrast enhancement. As compared to the monomeric counterpart (Gd-TESMA), the tetrameric Gd(4)-TESMA probe shows a clear advantage regarding both sensitivity and imaging time window, allowing for a better characterization of atherosclerotic plaques. |
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