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Publication : Interleukin 1 receptor 1 and interleukin 1β regulate megakaryocyte maturation, platelet activation, and transcript profile during inflammation in mice and humans.

First Author  Beaulieu LM Year  2014
Journal  Arterioscler Thromb Vasc Biol Volume  34
Issue  3 Pages  552-64
PubMed ID  24458711 Mgi Jnum  J:222911
Mgi Id  MGI:5645885 Doi  10.1161/ATVBAHA.113.302700
Citation  Beaulieu LM, et al. (2014) Interleukin 1 receptor 1 and interleukin 1beta regulate megakaryocyte maturation, platelet activation, and transcript profile during inflammation in mice and humans. Arterioscler Thromb Vasc Biol 34(3):552-64
abstractText  OBJECTIVE: Interleukin 1 Receptor 1 (IL1R1) and its ligand, IL1beta, are upregulated in cardiovascular disease, obesity, and infection. Previously, we reported a higher level of IL1R1 transcripts in platelets from obese individuals of the Framingham Heart Study (FHS), but its functional effect in platelets has never been described. Additionally, IL1beta levels are increased in atherosclerotic plaques and in bacterial infections. The aim of this work is to determine whether IL1beta, through IL1R1, can activate platelets and megakaryocytes to promote atherothrombosis. APPROACH AND RESULTS: We found that IL1beta-related genes from platelets, as measured in 1819 FHS participants, were associated with increased body mass index, and a direct relationship was shown in wild-type mice fed a high-fat diet. Mechanistically, IL1beta activated nuclear factor-kappaB and mitogen-activated protein kinase signaling pathways in megakaryocytes. IL1beta, through IL1R1, increased ploidy of megakaryocytes to 64+ N by 2-fold over control. IL1beta increased agonist-induced platelet aggregation by 1.2-fold with thrombin and 4.2-fold with collagen. IL1beta increased adhesion to both collagen and fibrinogen, and heterotypic aggregation by 1.9-fold over resting. High fat diet-enhanced platelet adhesion was absent in IL1R1(-/-) mice. Wild-type mice infected with Porphyromonas gingivalis had circulating heterotypic aggregates (1.5-fold more than control at 24 hours and 6.2-fold more at 6 weeks) that were absent in infected IL1R1(-/-) and IL1beta(-/-) mice. CONCLUSIONS: In summary, IL1R1- and IL1beta-related transcripts are elevated in the setting of obesity. IL1R1/IL1beta augment both megakaryocyte and platelet functions, thereby promoting a prothrombotic environment during infection and obesity; potentially contributing to the development of atherothrombotic disease.
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