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Lower HDL-C levels are associated with higher expressions of CD16 on monocyte subsets in coronary atherosclerosis
Background: Increased expressions of CD16 on classical monocytes precede their transition to intermediate monocytes. Thus far, the influence of lipids on the expression of CD14 and CD16 on monocyte subsets in coronary atherosclerosis (CA) remains unclear. The aim of this study was to investigate the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484662/ https://www.ncbi.nlm.nih.gov/pubmed/32922178 http://dx.doi.org/10.7150/ijms.47998 |
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author | Xiang, Yang Liang, Bin Zhang, Xiaokang Zheng, Fang |
author_facet | Xiang, Yang Liang, Bin Zhang, Xiaokang Zheng, Fang |
author_sort | Xiang, Yang |
collection | PubMed |
description | Background: Increased expressions of CD16 on classical monocytes precede their transition to intermediate monocytes. Thus far, the influence of lipids on the expression of CD14 and CD16 on monocyte subsets in coronary atherosclerosis (CA) remains unclear. The aim of this study was to investigate the underlying association between blood lipids and the expression of CD14 and CD16 on monocyte subsets. Methods: This study enrolled 112 healthy controls and 110 CA patients. Monocyte subsets [CD14(++)CD16(-) (classical), CD14(++)CD16(+) (intermediate) and CD14(+)CD16(++) (non-classical)] were analyzed by flow cytometry. Median fluorescent intensity (MFI) was used to evaluate the expression levels of CD14 and CD16 on monocyte subsets. Results: Compared with the control group, the expression of CD16 was significantly increased on all three monocyte subsets in the patient group. Correlation analysis revealed that serum HDL-C was inversely associated with the expression of CD16 on intermediate monocytes after Bonferroni correction in the control group. In addition, a significant decrease in classical monocytes and an increase in intermediate monocytes were detected in patients. In linear regression analysis, intermediate monocytes showed an inverse association with serum HDL-C in the control group. Although CD14 was correlated with serum TC and HDL-C, there was no statistical difference in CD14 expression between the two groups. Conclusion: Low serum HDL-C may induce upregulation of CD16 on classical monocytes, which may in turn lead to the increase of intermediate monocytes in coronary atherosclerosis patients. |
format | Online Article Text |
id | pubmed-7484662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-74846622020-09-12 Lower HDL-C levels are associated with higher expressions of CD16 on monocyte subsets in coronary atherosclerosis Xiang, Yang Liang, Bin Zhang, Xiaokang Zheng, Fang Int J Med Sci Research Paper Background: Increased expressions of CD16 on classical monocytes precede their transition to intermediate monocytes. Thus far, the influence of lipids on the expression of CD14 and CD16 on monocyte subsets in coronary atherosclerosis (CA) remains unclear. The aim of this study was to investigate the underlying association between blood lipids and the expression of CD14 and CD16 on monocyte subsets. Methods: This study enrolled 112 healthy controls and 110 CA patients. Monocyte subsets [CD14(++)CD16(-) (classical), CD14(++)CD16(+) (intermediate) and CD14(+)CD16(++) (non-classical)] were analyzed by flow cytometry. Median fluorescent intensity (MFI) was used to evaluate the expression levels of CD14 and CD16 on monocyte subsets. Results: Compared with the control group, the expression of CD16 was significantly increased on all three monocyte subsets in the patient group. Correlation analysis revealed that serum HDL-C was inversely associated with the expression of CD16 on intermediate monocytes after Bonferroni correction in the control group. In addition, a significant decrease in classical monocytes and an increase in intermediate monocytes were detected in patients. In linear regression analysis, intermediate monocytes showed an inverse association with serum HDL-C in the control group. Although CD14 was correlated with serum TC and HDL-C, there was no statistical difference in CD14 expression between the two groups. Conclusion: Low serum HDL-C may induce upregulation of CD16 on classical monocytes, which may in turn lead to the increase of intermediate monocytes in coronary atherosclerosis patients. Ivyspring International Publisher 2020-08-01 /pmc/articles/PMC7484662/ /pubmed/32922178 http://dx.doi.org/10.7150/ijms.47998 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Xiang, Yang Liang, Bin Zhang, Xiaokang Zheng, Fang Lower HDL-C levels are associated with higher expressions of CD16 on monocyte subsets in coronary atherosclerosis |
title | Lower HDL-C levels are associated with higher expressions of CD16 on monocyte subsets in coronary atherosclerosis |
title_full | Lower HDL-C levels are associated with higher expressions of CD16 on monocyte subsets in coronary atherosclerosis |
title_fullStr | Lower HDL-C levels are associated with higher expressions of CD16 on monocyte subsets in coronary atherosclerosis |
title_full_unstemmed | Lower HDL-C levels are associated with higher expressions of CD16 on monocyte subsets in coronary atherosclerosis |
title_short | Lower HDL-C levels are associated with higher expressions of CD16 on monocyte subsets in coronary atherosclerosis |
title_sort | lower hdl-c levels are associated with higher expressions of cd16 on monocyte subsets in coronary atherosclerosis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484662/ https://www.ncbi.nlm.nih.gov/pubmed/32922178 http://dx.doi.org/10.7150/ijms.47998 |
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