Expression of CARD8 in human atherosclerosis and its regulation of inflammatory proteins in human endothelial cellsShow others and affiliations
2020 (English)In: Scientific Reports, E-ISSN 2045-2322, Vol. 10, no 1, article id 19108
Article in journal (Refereed) Published
Abstract [en]
The Caspase activation and recruitment domain 8 (CARD8) protein is a component of innate immunity and overexpression of CARD8 mRNA was previously identified in atherosclerosis. However, very little is known about the regulation of CARD8 in endothelial cells and atherosclerosis. The aim of this study was to investigate CARD8 in the regulation of cytokine and chemokine expression in endothelial cells. Sections of human atherosclerotic lesions and non-atherosclerotic arteries were immunostained for CARD8 protein. Expression of CARD8 was correlated to mediators of inflammation in atherosclerotic lesions using Biobank of Karolinska Endarterectomies microarray data. The CARD8 mRNA was knocked-down in human umbilical vein endothelial cells (HUVECs) in vitro, followed by quantitative RT-PCR analysis and OLINK Proteomics. Endothelial and smooth muscle cells in arterial tissue expressed CARD8 and CARD8 correlated with vWF, CD163 and the expression of inflammatory genes, such as CXCL1, CXCL6 and PDGF-A in plaque. Knock-down of CARD8 in HUVECs significantly altered proteins involved in inflammatory response, such as CXCL1, CXCL6, PDGF-A, MCP-1 and IL-6. The present study suggest that CARD8 regulate the expression of cytokines and chemokines in endothelial cells and atherosclerotic lesions, suggesting that CARD8 plays a significant role in endothelial activation.
Place, publisher, year, edition, pages
Nature Publishing Group, 2020. Vol. 10, no 1, article id 19108
Keywords [en]
CARD8, atherosclerosis, chemokines, chronic inflammation, diagnostic markers, innate immunity, interleukins, mechanisms of disease
National Category
Cell and Molecular Biology Cardiac and Cardiovascular Systems
Research subject
Medicine
Identifiers
URN: urn:nbn:se:oru:diva-87251DOI: 10.1038/s41598-020-73600-4ISI: 000587146400001PubMedID: 33154409Scopus ID: 2-s2.0-85095132771OAI: oai:DiVA.org:oru-87251DiVA, id: diva2:1499195
Funder
Knowledge FoundationSwedish Heart Lung Foundation
Note
An Author Correction to this article was published in Sci Rep. 2021 Apr 19;11(1):8852. doi: 10.1038/s41598-021-88467-2.
2020-11-072020-11-072022-09-15Bibliographically approved