Cargando…
Assessment of Albumin ECM Accumulation and Inflammation as Novel In Vivo Diagnostic Targets for Multi-Target MR Imaging
SIMPLE SUMMARY: Atherosclerosis is an inflammatory disease associated with extracellular matrix remodeling. It is characterized by endothelial dysfunction with albumin influx into the vessel wall and macrophage accumulation in atherosclerotic lesions. Non-invasive magnetic resonance imaging (MRI) al...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533611/ https://www.ncbi.nlm.nih.gov/pubmed/34681063 http://dx.doi.org/10.3390/biology10100964 |
_version_ | 1784587355703738368 |
---|---|
author | Möckel, Jana Brangsch, Julia Reimann, Carolin Kaufmann, Jan O. Sack, Ingolf Mangarova, Dilyana B. Kader, Avan Taupitz, Matthias Adams, Lisa C. Keller, Sarah Ludwig, Antje Hamm, Bernd Botnar, Rene M. Makowski, Marcus R. |
author_facet | Möckel, Jana Brangsch, Julia Reimann, Carolin Kaufmann, Jan O. Sack, Ingolf Mangarova, Dilyana B. Kader, Avan Taupitz, Matthias Adams, Lisa C. Keller, Sarah Ludwig, Antje Hamm, Bernd Botnar, Rene M. Makowski, Marcus R. |
author_sort | Möckel, Jana |
collection | PubMed |
description | SIMPLE SUMMARY: Atherosclerosis is an inflammatory disease associated with extracellular matrix remodeling. It is characterized by endothelial dysfunction with albumin influx into the vessel wall and macrophage accumulation in atherosclerotic lesions. Non-invasive magnetic resonance imaging (MRI) allows for the assessment of the molecular components of the plaque and vessel wall by using two different target-specific MRI contrast agents in one imaging session. Therefore, multi-target MRI is a promising method to improve diagnosis and treatment monitoring in patients with atherosclerosis. ABSTRACT: Atherosclerosis is a progressive inflammatory vascular disease characterized by endothelial dysfunction and plaque burden. Extracellular matrix (ECM)-associated plasma proteins play an important role in disease development. Our magnetic resonance imaging (MRI) study investigates the feasibility of using two different molecular MRI probes for the simultaneous assessment of ECM-associated intraplaque albumin deposits caused by endothelial damage and progressive inflammation in atherosclerosis. Male apolipoprotein E-deficient (ApoE(-/-))-mice were fed a high-fat diet (HFD) for 2 or 4 months. Another ApoE(-/-)-group was treated with pravastatin and received a HFD for 4 months. T1- and T2*-weighted MRI was performed before and after albumin-specific MRI probe (gadofosveset) administration and a macrophage-specific contrast agent (ferumoxytol). Thereafter, laser ablation inductively coupled plasma mass spectrometry and histology were performed. With advancing atherosclerosis, albumin-based MRI signal enhancement and ferumoxytol-induced signal loss areas in T2*-weighted MRI increased. Significant correlations between contrast-to-noise-ratio (CNR) post-gadofosveset and albumin stain (R(2) = 0.78, p < 0.05), and signal loss areas in T2*-weighted MRI with Perls’ Prussian blue stain (R(2) = 0.83, p < 0.05) were observed. No interference of ferumoxytol with gadofosveset enhancement was detectable. Pravastatin led to decreased inflammation and intraplaque albumin. Multi-target MRI combining ferumoxytol and gadofosveset is a promising method to improve diagnosis and treatment monitoring in atherosclerosis. |
format | Online Article Text |
id | pubmed-8533611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85336112021-10-23 Assessment of Albumin ECM Accumulation and Inflammation as Novel In Vivo Diagnostic Targets for Multi-Target MR Imaging Möckel, Jana Brangsch, Julia Reimann, Carolin Kaufmann, Jan O. Sack, Ingolf Mangarova, Dilyana B. Kader, Avan Taupitz, Matthias Adams, Lisa C. Keller, Sarah Ludwig, Antje Hamm, Bernd Botnar, Rene M. Makowski, Marcus R. Biology (Basel) Article SIMPLE SUMMARY: Atherosclerosis is an inflammatory disease associated with extracellular matrix remodeling. It is characterized by endothelial dysfunction with albumin influx into the vessel wall and macrophage accumulation in atherosclerotic lesions. Non-invasive magnetic resonance imaging (MRI) allows for the assessment of the molecular components of the plaque and vessel wall by using two different target-specific MRI contrast agents in one imaging session. Therefore, multi-target MRI is a promising method to improve diagnosis and treatment monitoring in patients with atherosclerosis. ABSTRACT: Atherosclerosis is a progressive inflammatory vascular disease characterized by endothelial dysfunction and plaque burden. Extracellular matrix (ECM)-associated plasma proteins play an important role in disease development. Our magnetic resonance imaging (MRI) study investigates the feasibility of using two different molecular MRI probes for the simultaneous assessment of ECM-associated intraplaque albumin deposits caused by endothelial damage and progressive inflammation in atherosclerosis. Male apolipoprotein E-deficient (ApoE(-/-))-mice were fed a high-fat diet (HFD) for 2 or 4 months. Another ApoE(-/-)-group was treated with pravastatin and received a HFD for 4 months. T1- and T2*-weighted MRI was performed before and after albumin-specific MRI probe (gadofosveset) administration and a macrophage-specific contrast agent (ferumoxytol). Thereafter, laser ablation inductively coupled plasma mass spectrometry and histology were performed. With advancing atherosclerosis, albumin-based MRI signal enhancement and ferumoxytol-induced signal loss areas in T2*-weighted MRI increased. Significant correlations between contrast-to-noise-ratio (CNR) post-gadofosveset and albumin stain (R(2) = 0.78, p < 0.05), and signal loss areas in T2*-weighted MRI with Perls’ Prussian blue stain (R(2) = 0.83, p < 0.05) were observed. No interference of ferumoxytol with gadofosveset enhancement was detectable. Pravastatin led to decreased inflammation and intraplaque albumin. Multi-target MRI combining ferumoxytol and gadofosveset is a promising method to improve diagnosis and treatment monitoring in atherosclerosis. MDPI 2021-09-27 /pmc/articles/PMC8533611/ /pubmed/34681063 http://dx.doi.org/10.3390/biology10100964 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Möckel, Jana Brangsch, Julia Reimann, Carolin Kaufmann, Jan O. Sack, Ingolf Mangarova, Dilyana B. Kader, Avan Taupitz, Matthias Adams, Lisa C. Keller, Sarah Ludwig, Antje Hamm, Bernd Botnar, Rene M. Makowski, Marcus R. Assessment of Albumin ECM Accumulation and Inflammation as Novel In Vivo Diagnostic Targets for Multi-Target MR Imaging |
title | Assessment of Albumin ECM Accumulation and Inflammation as Novel In Vivo Diagnostic Targets for Multi-Target MR Imaging |
title_full | Assessment of Albumin ECM Accumulation and Inflammation as Novel In Vivo Diagnostic Targets for Multi-Target MR Imaging |
title_fullStr | Assessment of Albumin ECM Accumulation and Inflammation as Novel In Vivo Diagnostic Targets for Multi-Target MR Imaging |
title_full_unstemmed | Assessment of Albumin ECM Accumulation and Inflammation as Novel In Vivo Diagnostic Targets for Multi-Target MR Imaging |
title_short | Assessment of Albumin ECM Accumulation and Inflammation as Novel In Vivo Diagnostic Targets for Multi-Target MR Imaging |
title_sort | assessment of albumin ecm accumulation and inflammation as novel in vivo diagnostic targets for multi-target mr imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533611/ https://www.ncbi.nlm.nih.gov/pubmed/34681063 http://dx.doi.org/10.3390/biology10100964 |
work_keys_str_mv | AT mockeljana assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT brangschjulia assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT reimanncarolin assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT kaufmannjano assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT sackingolf assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT mangarovadilyanab assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT kaderavan assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT taupitzmatthias assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT adamslisac assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT kellersarah assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT ludwigantje assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT hammbernd assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT botnarrenem assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging AT makowskimarcusr assessmentofalbuminecmaccumulationandinflammationasnovelinvivodiagnostictargetsformultitargetmrimaging |