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Colocalization of Erythrocytes and Vascular Calcification in Human Atherosclerosis: A Systematic Histomorphometric Analysis

Background  Intimal calcification typically develops in advanced atherosclerosis, and microcalcification may promote plaque progression and instability. Conversely, intraplaque hemorrhage and erythrocyte extravasation may stimulate osteoblastic differentiation and intralesional calcium phosphate dep...

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Autores principales: Böhm, Elsa Wilma, Pavlaki, Maria, Chalikias, Georgios, Mikroulis, Dimitrios, Georgiadis, George S., Tziakas, Dimitrios N., Konstantinides, Stavros, Schäfer, Katrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046517/
https://www.ncbi.nlm.nih.gov/pubmed/33870075
http://dx.doi.org/10.1055/s-0041-1725042
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author Böhm, Elsa Wilma
Pavlaki, Maria
Chalikias, Georgios
Mikroulis, Dimitrios
Georgiadis, George S.
Tziakas, Dimitrios N.
Konstantinides, Stavros
Schäfer, Katrin
author_facet Böhm, Elsa Wilma
Pavlaki, Maria
Chalikias, Georgios
Mikroulis, Dimitrios
Georgiadis, George S.
Tziakas, Dimitrios N.
Konstantinides, Stavros
Schäfer, Katrin
author_sort Böhm, Elsa Wilma
collection PubMed
description Background  Intimal calcification typically develops in advanced atherosclerosis, and microcalcification may promote plaque progression and instability. Conversely, intraplaque hemorrhage and erythrocyte extravasation may stimulate osteoblastic differentiation and intralesional calcium phosphate deposition. The presence of erythrocytes and their main cellular components (membranes, hemoglobin, and iron) and colocalization with calcification has never been systematically studied. Methods and Results  We examined three types of diseased vascular tissue specimens, namely, degenerative aortic valve stenosis ( n  = 46), atherosclerotic carotid artery plaques ( n  = 9), and abdominal aortic aneurysms ( n  = 14). Biomaterial was obtained from symptomatic patients undergoing elective aortic valve replacement, carotid artery endatherectomy, or aortic aneurysm repair, respectively. Serial sections were stained using Masson–Goldner trichrome, Alizarin red S, and Perl's iron stain to visualize erythrocytes, extracelluar matrix and osteoid, calcium phosphate deposition, or the presence of iron and hemosiderin, respectively. Immunohistochemistry was employed to detect erythrocyte membranes (CD235a), hemoglobin or the hemoglobin scavenger receptor (CD163), endothelial cells (CD31), myofibroblasts (SMA), mesenchymal cells (osteopontin), or osteoblasts (periostin). Our analyses revealed a varying degree of intraplaque hemorrhage and that the majority of extravasated erythrocytes were lysed. Osteoid and calcifications also were frequently present, and erythrocyte membranes were significantly more prevalent in areas with calcification. Areas with extravasated erythrocytes frequently contained CD163-positive cells, although calcification also occurred in areas without CD163 immunosignals. Conclusion  Our findings underline the presence of extravasated erythrocytes and their membranes in different types of vascular lesions, and their association with areas of calcification suggests an active role of erythrocytes in vascular disease processes.
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spelling pubmed-80465172021-04-15 Colocalization of Erythrocytes and Vascular Calcification in Human Atherosclerosis: A Systematic Histomorphometric Analysis Böhm, Elsa Wilma Pavlaki, Maria Chalikias, Georgios Mikroulis, Dimitrios Georgiadis, George S. Tziakas, Dimitrios N. Konstantinides, Stavros Schäfer, Katrin TH Open Background  Intimal calcification typically develops in advanced atherosclerosis, and microcalcification may promote plaque progression and instability. Conversely, intraplaque hemorrhage and erythrocyte extravasation may stimulate osteoblastic differentiation and intralesional calcium phosphate deposition. The presence of erythrocytes and their main cellular components (membranes, hemoglobin, and iron) and colocalization with calcification has never been systematically studied. Methods and Results  We examined three types of diseased vascular tissue specimens, namely, degenerative aortic valve stenosis ( n  = 46), atherosclerotic carotid artery plaques ( n  = 9), and abdominal aortic aneurysms ( n  = 14). Biomaterial was obtained from symptomatic patients undergoing elective aortic valve replacement, carotid artery endatherectomy, or aortic aneurysm repair, respectively. Serial sections were stained using Masson–Goldner trichrome, Alizarin red S, and Perl's iron stain to visualize erythrocytes, extracelluar matrix and osteoid, calcium phosphate deposition, or the presence of iron and hemosiderin, respectively. Immunohistochemistry was employed to detect erythrocyte membranes (CD235a), hemoglobin or the hemoglobin scavenger receptor (CD163), endothelial cells (CD31), myofibroblasts (SMA), mesenchymal cells (osteopontin), or osteoblasts (periostin). Our analyses revealed a varying degree of intraplaque hemorrhage and that the majority of extravasated erythrocytes were lysed. Osteoid and calcifications also were frequently present, and erythrocyte membranes were significantly more prevalent in areas with calcification. Areas with extravasated erythrocytes frequently contained CD163-positive cells, although calcification also occurred in areas without CD163 immunosignals. Conclusion  Our findings underline the presence of extravasated erythrocytes and their membranes in different types of vascular lesions, and their association with areas of calcification suggests an active role of erythrocytes in vascular disease processes. Georg Thieme Verlag KG 2021-04-14 /pmc/articles/PMC8046517/ /pubmed/33870075 http://dx.doi.org/10.1055/s-0041-1725042 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. ( https://creativecommons.org/licenses/by/4.0/ ) https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Böhm, Elsa Wilma
Pavlaki, Maria
Chalikias, Georgios
Mikroulis, Dimitrios
Georgiadis, George S.
Tziakas, Dimitrios N.
Konstantinides, Stavros
Schäfer, Katrin
Colocalization of Erythrocytes and Vascular Calcification in Human Atherosclerosis: A Systematic Histomorphometric Analysis
title Colocalization of Erythrocytes and Vascular Calcification in Human Atherosclerosis: A Systematic Histomorphometric Analysis
title_full Colocalization of Erythrocytes and Vascular Calcification in Human Atherosclerosis: A Systematic Histomorphometric Analysis
title_fullStr Colocalization of Erythrocytes and Vascular Calcification in Human Atherosclerosis: A Systematic Histomorphometric Analysis
title_full_unstemmed Colocalization of Erythrocytes and Vascular Calcification in Human Atherosclerosis: A Systematic Histomorphometric Analysis
title_short Colocalization of Erythrocytes and Vascular Calcification in Human Atherosclerosis: A Systematic Histomorphometric Analysis
title_sort colocalization of erythrocytes and vascular calcification in human atherosclerosis: a systematic histomorphometric analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046517/
https://www.ncbi.nlm.nih.gov/pubmed/33870075
http://dx.doi.org/10.1055/s-0041-1725042
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