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CD163+ macrophages are associated with a vulnerable plaque phenotype in human carotid plaques
Macrophages are a functionally heterogeneous group of immune cells abundant in atherosclerotic plaques. Macrophages expressing CD163 are associated with intraplaque hemorrhage and have previously been considered atheroprotective. However, in a recent study CD163-deficient atherosclerotic ApoE(−/−) m...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463157/ https://www.ncbi.nlm.nih.gov/pubmed/32873809 http://dx.doi.org/10.1038/s41598-020-71110-x |
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author | Bengtsson, Eva Hultman, Karin Edsfeldt, Andreas Persson, Ana Nitulescu, Mihaela Nilsson, Jan Gonçalves, Isabel Björkbacka, Harry |
author_facet | Bengtsson, Eva Hultman, Karin Edsfeldt, Andreas Persson, Ana Nitulescu, Mihaela Nilsson, Jan Gonçalves, Isabel Björkbacka, Harry |
author_sort | Bengtsson, Eva |
collection | PubMed |
description | Macrophages are a functionally heterogeneous group of immune cells abundant in atherosclerotic plaques. Macrophages expressing CD163 are associated with intraplaque hemorrhage and have previously been considered atheroprotective. However, in a recent study CD163-deficient atherosclerotic ApoE(−/−) mice exhibited smaller and less complex plaques, suggesting a proatherogenic role of CD163. Previous smaller studies on CD163+ macrophages and plaque stability in humans have yielded diverging results. Here we assessed the association of CD163+ cells to plaque vulnerability in a large cohort of human carotid plaques. CD163 protein expression was analyzed by immunohistochemistry in 200 human carotid plaques removed by endarterectomy from 103 patients with and 93 patients without cerebrovascular symptoms. Furthermore, CD163 mRNA expression was analyzed in 66 of the plaques. Both protein and mRNA expression of CD163 was higher in plaques from symptomatic patients and in plaques with high vulnerability index. CD163+ macrophages were primarily found in shoulder regions and in the center of the plaques. The present data show that CD163 is associated with increased plaque vulnerability in human carotid plaques, supporting the notion that CD163+ macrophages could contribute to clinical events. |
format | Online Article Text |
id | pubmed-7463157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74631572020-09-03 CD163+ macrophages are associated with a vulnerable plaque phenotype in human carotid plaques Bengtsson, Eva Hultman, Karin Edsfeldt, Andreas Persson, Ana Nitulescu, Mihaela Nilsson, Jan Gonçalves, Isabel Björkbacka, Harry Sci Rep Article Macrophages are a functionally heterogeneous group of immune cells abundant in atherosclerotic plaques. Macrophages expressing CD163 are associated with intraplaque hemorrhage and have previously been considered atheroprotective. However, in a recent study CD163-deficient atherosclerotic ApoE(−/−) mice exhibited smaller and less complex plaques, suggesting a proatherogenic role of CD163. Previous smaller studies on CD163+ macrophages and plaque stability in humans have yielded diverging results. Here we assessed the association of CD163+ cells to plaque vulnerability in a large cohort of human carotid plaques. CD163 protein expression was analyzed by immunohistochemistry in 200 human carotid plaques removed by endarterectomy from 103 patients with and 93 patients without cerebrovascular symptoms. Furthermore, CD163 mRNA expression was analyzed in 66 of the plaques. Both protein and mRNA expression of CD163 was higher in plaques from symptomatic patients and in plaques with high vulnerability index. CD163+ macrophages were primarily found in shoulder regions and in the center of the plaques. The present data show that CD163 is associated with increased plaque vulnerability in human carotid plaques, supporting the notion that CD163+ macrophages could contribute to clinical events. Nature Publishing Group UK 2020-09-01 /pmc/articles/PMC7463157/ /pubmed/32873809 http://dx.doi.org/10.1038/s41598-020-71110-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bengtsson, Eva Hultman, Karin Edsfeldt, Andreas Persson, Ana Nitulescu, Mihaela Nilsson, Jan Gonçalves, Isabel Björkbacka, Harry CD163+ macrophages are associated with a vulnerable plaque phenotype in human carotid plaques |
title | CD163+ macrophages are associated with a vulnerable plaque phenotype in human carotid plaques |
title_full | CD163+ macrophages are associated with a vulnerable plaque phenotype in human carotid plaques |
title_fullStr | CD163+ macrophages are associated with a vulnerable plaque phenotype in human carotid plaques |
title_full_unstemmed | CD163+ macrophages are associated with a vulnerable plaque phenotype in human carotid plaques |
title_short | CD163+ macrophages are associated with a vulnerable plaque phenotype in human carotid plaques |
title_sort | cd163+ macrophages are associated with a vulnerable plaque phenotype in human carotid plaques |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463157/ https://www.ncbi.nlm.nih.gov/pubmed/32873809 http://dx.doi.org/10.1038/s41598-020-71110-x |
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