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Adenosine signaling during acute and chronic disease states

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TLDR
Key observations are discussed that define the beneficial and detrimental aspects of adenosine signaling during acute and chronic disease states with an emphasis on cellular processes, such as inflammatory cell regulation, vascular barrier function, and tissue fibrosis.
Abstract
Adenosine is a signaling nucleoside that is produced following tissue injury, particularly injury involving ischemia and hypoxia. The production of extracellular adenosine and its subsequent signaling through adenosine receptors plays an important role in orchestrating injury responses in multiple organs. There are four adenosine receptors that are widely distributed on immune, epithelial, endothelial, neuronal,and stromal cells throughout the body. Interestingly, these receptors are subject to altered regulation following injury. Studies in mouse models and human cells and tissues have identified that the production of adenosine and its subsequent signaling through its receptors plays largely beneficial roles in acute disease states, with the exception of brain injury. In contrast, if elevated adenosine levels are sustained beyond the acute injury phase, adenosine responses can become detrimental by activating pathways that promote tissue injury and fibrosis. Understanding when during the course of disease adenosine signaling is beneficial as opposed to detrimental and defining the mechanisms involved will be critical for the advancement of adenosine-based therapies for acute and chronic diseases. The purpose of this review is to discuss key observations that define the beneficial and detrimental aspects of adenosine signaling during acute and chronic disease states with an emphasis on cellular processes, such as inflammatory cell regulation, vascular barrier function, and tissue fibrosis.

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References
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Journal ArticleDOI

Molecular action of methotrexate in inflammatory diseases

TL;DR: In confirmation of this mechanism of action, recent studies in both animals and patients suggest that adenosine-receptor antagonists, among which is caffeine, reverse or prevent the anti-inflammatory effects of methotrexate.
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Inhaled adenosine and guanosine on airway resistance in normal and asthmatic subjects

TL;DR: The airway response to inhaled nucleosides, adenosine (6.7 × 10-4-6.4 mg/ml) and guanosine (7.3 × 10 -4-1.4mg/ml), was studied in normal and asthmatic subjects as discussed by the authors.
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A2A adenosine receptor induction inhibits IFN-gamma production in murine CD4+ T cells.

TL;DR: It is demonstrated here that signaling through the TCR causes a rapid (4-h) 5-fold increase in A2A adenosine receptor (AR) mRNA, which is correlated with a significant increase in the efficacy of A1AAR-mediated cAMP accumulation in T cells and provides a mechanism for limiting T cell activation and secondary macrophage activation in inflamed tissues.
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The A2B adenosine receptor protects against inflammation and excessive vascular adhesion

TL;DR: The A2BAR is identified as a new critical regulator of inflammation and vascular adhesion primarily via signals from hematopoietic cells to the vasculature, focusing attention on the receptor as a therapeutic target.
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Adenosine in bronchoalveolar lavage fluid in asthma.

TL;DR: The demonstration of physiologically relevant concentrations of adenosine in airway fluids of subjects with bronchial hyperreactivity to inhaledadenosine provides evidence for a role of endogenous adenosines in provoking bronchoconstriction in asthma.
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