Cardiovascular Research Centre, School of Medical Sciences, Faculty of Medicine and Health, Örebro University, 70182, Örebro, Sweden.
Laboratory of Immunobiology, Center for Bioelectronic Medicine, Department of Medicine, Karolinska Institute, Solna, Stockholm, Sweden.
Sci Rep. 2020 Nov 5;10(1):19108. doi: 10.1038/s41598-020-73600-4.
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.
Caspase 激活和募集结构域 8(CARD8)蛋白是先天免疫的一个组成部分,先前在动脉粥样硬化中鉴定出 CARD8 mRNA 的过表达。然而,关于 CARD8 在血管内皮细胞和动脉粥样硬化中的调节知之甚少。本研究旨在研究 CARD8 在血管内皮细胞中细胞因子和趋化因子表达的调节作用。对人动脉粥样硬化病变和非动脉粥样硬化动脉的组织切片进行 CARD8 蛋白免疫染色。使用 Karolinska 内膜切除术生物银行的微阵列数据,将 CARD8 的表达与动脉粥样硬化病变中的炎症介质相关联。在体外对人脐静脉内皮细胞(HUVEC)进行 CARD8 mRNA 敲低,然后进行定量 RT-PCR 分析和 OLINK 蛋白质组学分析。动脉组织中的内皮细胞和平滑肌细胞表达 CARD8,并且 CARD8 与 vWF、CD163 和炎症基因的表达相关,如斑块中的 CXCL1、CXCL6 和 PDGF-A。HUVEC 中的 CARD8 敲低显著改变了炎症反应相关的蛋白,如 CXCL1、CXCL6、PDGF-A、MCP-1 和 IL-6。本研究表明 CARD8 调节内皮细胞和动脉粥样硬化病变中细胞因子和趋化因子的表达,表明 CARD8 在血管内皮细胞激活中发挥重要作用。