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Difference of immune cell infiltration between stable and unstable carotid artery atherosclerosis
Atherosclerotic plaque instability contributes to ischaemic stroke and myocardial infarction. This study is to compare the abundance and difference of immune cell subtypes within unstable atherosclerotic tissues. CIBERSORT was used to speculate the proportions of 22 immune cell types based on a micr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8642673/ https://www.ncbi.nlm.nih.gov/pubmed/34729909 http://dx.doi.org/10.1111/jcmm.17018 |
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author | Gao, Jia Shi, Licheng Gu, Jianhua Zhang, Dandan Wang, Wenjun Zhu, Xuanfeng Liu, Jiannan |
author_facet | Gao, Jia Shi, Licheng Gu, Jianhua Zhang, Dandan Wang, Wenjun Zhu, Xuanfeng Liu, Jiannan |
author_sort | Gao, Jia |
collection | PubMed |
description | Atherosclerotic plaque instability contributes to ischaemic stroke and myocardial infarction. This study is to compare the abundance and difference of immune cell subtypes within unstable atherosclerotic tissues. CIBERSORT was used to speculate the proportions of 22 immune cell types based on a microarray of atherosclerotic carotid artery samples. R software was utilized to illustrate the bar plot, heat map and vioplot. The immune cell landscape in atherosclerosis was diverse, dominated by M2 macrophages, M0 macrophages, resting CD4 memory T cells and CD8 T cells. There was a significant difference in resting CD4 memory T cells (p = 0.032), T cells follicular helper (p = 0.033), M0 (p = 0.047) and M2 macrophages (p = 0.012) between stable and unstable atherosclerotic plaques. Compared with stable atherosclerotic plaques, unstable atherosclerotic plaques had a higher percentage of M2 macrophages. Moreover, correlation analysis indicated that the percentage of naïve CD4 T cells was strongly correlated with that of gamma delta T cells (r = 0.93, p < 0.001), while memory B cells were correlated with plasma cells (r = 0.85, p < 0.001). In summary, our study explored the abundance and difference of specific immune cell subgroups at unstable plaques, which would aid new immunotherapies for atherosclerosis. |
format | Online Article Text |
id | pubmed-8642673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86426732021-12-15 Difference of immune cell infiltration between stable and unstable carotid artery atherosclerosis Gao, Jia Shi, Licheng Gu, Jianhua Zhang, Dandan Wang, Wenjun Zhu, Xuanfeng Liu, Jiannan J Cell Mol Med Original Articles Atherosclerotic plaque instability contributes to ischaemic stroke and myocardial infarction. This study is to compare the abundance and difference of immune cell subtypes within unstable atherosclerotic tissues. CIBERSORT was used to speculate the proportions of 22 immune cell types based on a microarray of atherosclerotic carotid artery samples. R software was utilized to illustrate the bar plot, heat map and vioplot. The immune cell landscape in atherosclerosis was diverse, dominated by M2 macrophages, M0 macrophages, resting CD4 memory T cells and CD8 T cells. There was a significant difference in resting CD4 memory T cells (p = 0.032), T cells follicular helper (p = 0.033), M0 (p = 0.047) and M2 macrophages (p = 0.012) between stable and unstable atherosclerotic plaques. Compared with stable atherosclerotic plaques, unstable atherosclerotic plaques had a higher percentage of M2 macrophages. Moreover, correlation analysis indicated that the percentage of naïve CD4 T cells was strongly correlated with that of gamma delta T cells (r = 0.93, p < 0.001), while memory B cells were correlated with plasma cells (r = 0.85, p < 0.001). In summary, our study explored the abundance and difference of specific immune cell subgroups at unstable plaques, which would aid new immunotherapies for atherosclerosis. John Wiley and Sons Inc. 2021-11-03 2021-12 /pmc/articles/PMC8642673/ /pubmed/34729909 http://dx.doi.org/10.1111/jcmm.17018 Text en © 2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Gao, Jia Shi, Licheng Gu, Jianhua Zhang, Dandan Wang, Wenjun Zhu, Xuanfeng Liu, Jiannan Difference of immune cell infiltration between stable and unstable carotid artery atherosclerosis |
title | Difference of immune cell infiltration between stable and unstable carotid artery atherosclerosis |
title_full | Difference of immune cell infiltration between stable and unstable carotid artery atherosclerosis |
title_fullStr | Difference of immune cell infiltration between stable and unstable carotid artery atherosclerosis |
title_full_unstemmed | Difference of immune cell infiltration between stable and unstable carotid artery atherosclerosis |
title_short | Difference of immune cell infiltration between stable and unstable carotid artery atherosclerosis |
title_sort | difference of immune cell infiltration between stable and unstable carotid artery atherosclerosis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8642673/ https://www.ncbi.nlm.nih.gov/pubmed/34729909 http://dx.doi.org/10.1111/jcmm.17018 |
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