Adenosine, long known as a regulator of cardiovascular function, has recently been identified as a significant paracrine inhibitor of inflammation that acts primarily by activation of A2A adenosine receptors (A2AARs) on lymphoid or myeloid cells. In this issue of the JCI, Yang et al. describe a proinflammatory phenotype resulting from deletion of the gene encoding the A2B adenosine receptor (A2BAR) in the mouse, suggesting that activation of the A2BAR can also have antiinflammatory effects (see the related article beginning on page 1913). Nevertheless, the role of the A2BAR remains enigmatic since its activation can either stimulate or inhibit the release of proinflammatory cytokines in different cells and tissues.
Joel Linden
Title and authors | Publication | Year |
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Feedback effects of host-derived adenosine on enteropathogenic Escherichia coli
JK Crane, I Shulgina |
FEMS Immunology and Medical Microbiology | 2009 |
Reduced ligand affinity leads to an impaired function of the adenosine A2Areceptor of human granulocytes in sepsis
S Kreth, I Kaufmann, C Ledderose, B Luchting, M Thiel |
Journal of Cellular and Molecular Medicine | 2009 |
Adenosine regulates thrombomodulin and endothelial protein C receptor expression in folliculostellate cells of the pituitary gland
DA Rees, P Giles, MD Lewis, J Ham |
Purinergic Signalling | 2009 |
A2A adenosine receptor (AR) activation inhibits pro-inflammatory cytokine production by human CD4+ helper T cells and regulates Helicobacter-induced gastritis and bacterial persistence
Alam M, Kurtz C, Wilson J, Burnette B, Wiznerowicz E, Ross W, Rieger J, Figler R, Linden J, Crowe S, Ernst P |
Mucosal Immunology | 2009 |