Journal Article

CCL18 aggravates atherosclerosis by inducing CCR6-dependent T-cell influx and polarization

Nicolaes, Gerry A. F., Wichapong, Kanin, Atamas, Sergei P., Mees, Barend, Tacke, Frank, Heemskerk, Johan W. M., Curaj, Adelina, Jukema, J. Wouter, van Berkel, Theo J. C., Liehn, Elisa Anamaria, McColl, Shaun R., de Jager, Saskia C. A., Comerford, Iain, Biessen, Erik A. L., Singh, Anjana, Kraaijeveld, Adriaan O., Hammerich, Linda, Bot, Ilze, Hackeng, Tilman

2024

Overview

The CC chemokine ligand 18 (CCL18) is a chemokine highly expressed in chronic inflammation in humans. Recent observations of elevated CCL18 plasma levels in patients with acute cardiovascular syndromes prompted an investigation into the role of CCL18 in the pathogenesis of human and mouse atherosclerosis. CCL18 was profoundly upregulated in ruptured human atherosclerotic plaque, particularly within macrophages. Repeated administration of CCL18 in Western-type diet-fed mice or PCSK9 -overexpressing wild type (WT) mice led to increased plaque burden, enriched in CD3 T cells. In subsequent experimental and molecular modeling studies, we identified CCR6 as a functional receptor mediating CCL18 chemotaxis, intracellular Ca flux, and downstream signaling in human Jurkat and mouse T cells. CCL18 failed to induce these effects in murine spleen T cells with CCR6 deficiency. The ability of CCR6 to act as CCL18 receptor was confirmed in an inflammation model, where subcutaneous CCL18 injection induced profound focal skin inflammation in WT but not in mice. This inflammation featured edema and marked infiltration of various leukocyte subsets, including T cells with a Th17 signature, supporting CCR6's role as a Th17 chemotactic receptor. Notably, focal overexpression of CCL18 in plaques was associated with an increased presence of CCR6 (T) cells. Our studies are the first to identify the CCL18/CCR6 axis as a regulator of immune responses in advanced murine and human atherosclerosis.

• Publisher: Frontiers Media SA,Frontiers Media S.A
• Subject: Angina pectoris / Animals / Apolipoprotein E / Arteriosclerosis / Atherosclerosis / Atherosclerosis - immunology / Atherosclerosis - metabolism / Autopsies / Calcium (intracellular) / Calcium signalling / cardiovascular / Carotid arteries / CC chemokine receptors / CD3 antigen / Chemokines / Chemokines, CC - genetics / Chemokines, CC - metabolism / Chemotaxis / Cholesterol / Disease Models, Animal / Edema / Female / Females / Helper cells / Humans / Immunology / Inflammation / Intracellular signalling / Jurkat Cells / Lesions / Ligands / Lymphocytes / Lymphocytes T / Macrophages / Male / Mice / Mice, Inbred C57BL / Mice, Knockout / Mice, Knockout, ApoE / Molecular modelling / Pathology / plaque / Plaque, Atherosclerotic - immunology / Plasma levels / Receptors, CCR6 - genetics / Receptors, CCR6 - metabolism / T-Lymphocytes - immunology / T-Lymphocytes - metabolism / Th17 / Th17 Cells - immunology / Th17 Cells - metabolism / Veins & arteries