Decreased GPR55 expression links B-cell activation and vascular remodelling in atherosclerosis in early rheumatoid arthritis patients
Listed in
This article is not in any list yet, why not save it to one of your lists.Abstract
Objective
inflammation and repair responses may be involved in atherosclerosis in rheumatoid arthritis (RA), although mechanisms are unknown. GPR55 is a cannabinoid receptor expressed in hematopoietic and stromal tissues, which has been implicated in atherosclerosis in mouse models, but evidence in humans is lacking. Our aim was to evaluate GPR55 expression in leukocyte populations in RA patients and their potential role in atherosclerosis.
Methods
GPR55 expression was quantified by flow cytometry in 63 untreated RA patients, 11 arthralgia individuals and 36 controls. Atherosclerosis was assessed by Doppler-ultrasound. Cytokines were measured by immunoassays, and serum proteomics were performed by a high-throughput targeted panel. In vitro cultures were performed with mononuclear cells from healthy donors.
Results
Decreased GPR55 expression in B-cells and monocytes was found in RA, whereas no differences were observed in arthralgia. Public datasets validated these findings. B-cell GPR55 expression was unrelated to clinical features, risk factors and atherosclerosis in RA, but exhibited divergent associations with leukocyte populations. GPR55 expression was associated with proinflammatory cytokines, and proteomic signatures related to vascular remodelling and B-cell responses in RA. These associations were dependent on the atherosclerosis status. LPS exposure in vitro decreased GPR55 expression in B-cells in a dose-dependent manner, which overlapped increasing CB86 expression.
Conclusions
Reduced GPR55 expression hallmarked B-cells and monocyte subsets in early RA. GPR55 expression was linked to B-cell activation-related pathways, presumably via T-cell independent mechanisms, and vascular remodelling. GPR55 may be a novel hub to understand the crosstalk between immune circuits and maladaptive responses in atherosclerosis.