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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

Detrimental effects of adenosine signaling in sickle cell disease

TL;DR: It is shown that adenosine A2B receptor (A2BR)-mediated induction of 2,3-diphosphoglycerate, an erythrocyte-specific metabolite that decreases the oxygen binding affinity of hemoglobin, underlies the induction of ery Throcyte sickling by excessAdenosine both in cultured human red blood cells and in SCD transgenic mice.
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Past, present and future of A2A adenosine receptor antagonists in the therapy of Parkinson's disease

TL;DR: A considerable body of data indicates that in addition to ameliorating motor symptoms, adenosine A(2A)R antagonists may also prevent neurodegeneration.
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Signaling through the A2B Adenosine Receptor Dampens Endotoxin-Induced Acute Lung Injury

TL;DR: Initial insight was gained from in vitro studies of cultured endothelia or epithelia exposed to inflammatory mediators showing time-dependent induction of the A2BAR and murine studies of endotoxin-induced lung injury identified an almost 4.6-fold induction of A 2BAR transcript and corresponding protein induction with LPS exposure.
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Ethanol-induced activation of adenine nucleotide turnover. Evidence for a role of acetate.

TL;DR: Data indicate that both ethanol and acetate increase purine nucleotide degradation by enhancing the turnover of the adenineucleotide pool, which supports the hypothesis that acetate metabolism contributes to the increased production of urate associated with ethanol intake.
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Physiological Roles of Vascular Nucleoside Transporters

TL;DR: Vascular NTs are critical in modulating adenosine-mediated responses during conditions such as inflammation or hypoxia, which among others plays an important role in tissue protection during acute injury.
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