Expression of Interleukin 6 signaling receptors in carotid atherosclerosis

Author:

Ziegler Louise12ORCID,Lundqvist Jasmin3,Dreij Kristian4,Wallén Håkan15,de Faire Ulf67,Paulsson-Berne Gabrielle3,Hedin Ulf89,Matic Ljubica9,Gigante Bruna35

Affiliation:

1. Department of Clinical Sciences, Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden

2. Department of Medicine, Danderyd Hospital, Stockholm, Sweden

3. Cardiovascular Medicine Unit, Department of Medicine, Karolinska Institutet, Stockholm, Sweden

4. Unit of Biochemical Toxicology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden

5. Department of Cardiology, Danderyd Hospital, Stockholm, Sweden

6. Unit of Cardiovascular and Nutritional Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden

7. Department of Cardiology, Karolinska University Hospital, Stockholm, Sweden

8. Department of Vascular Surgery, Karolinska University Hospital, Stockholm, Sweden

9. Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden

Abstract

Interleukin (IL) 6 contributes to atherosclerotic plaque development through IL6 membrane-bound (IL6R and gp130) and soluble (sIL6R and sgp130) receptors. We investigated IL6 receptor expression in carotid plaques and its correlation with circulating IL6 and soluble receptor levels. Plasma samples and carotid plaques were obtained from 78 patients in the Biobank of Karolinska Endarterectomies study. IL6, sIL6R, and sgp130 were measured in plasma and IL6, IL6R, sIL6R, GP130, and s GP130-RAPS (s GP130) gene expression assessed in carotid plaques. Correlations between plaque IL6 signaling gene expression and plasma levels were determined by Spearman’s correlation. Differences in plasma and gene expression levels between patients with ( n = 53) and without ( n = 25) a history of a cerebral event and statin-treated ( n = 65) and non-treated ( n = 11), were estimated by Kruskal–Wallis. IL6 and its receptors were all expressed in carotid plaques. There was a positive, borderline significant, moderate correlation between plasma IL6 and sIL6R and the respective gene expression levels (rho 0.23 and 0.22, both p = 0.05). IL6R expression was higher in patients with a history of a cerebrovascular event compared to those without ( p = 0.007). Statin-treated had higher IL6R, sIL6R, and s GP130 expression levels and plasma sIL6R compared to non-treated patients (all p < 0.05). In conclusion, all components of the IL6 signaling pathways are expressed in carotid artery plaques and IL6 and sIL6R plasma levels correlate moderately with IL6 and sIL6R. Our data suggest that IL6 signaling in the circulation might mirror the system activity in the plaque, thus adding novel perspectives to the role of IL6 signaling in atherosclerosis.

Funder

Swedish heart and lung foundation

the Strategic Cardiovascular Programs of Karolinska Institutet

the Swen and Ebba Hagberg foundation

svenska sällskapet för medicinsk forskning

the Danderyd Hospital Fond 176

the Stockholm County Council

Vetenskapsrådet

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine

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