Increased extracellular adenosine in Drosophila that are deficient in adenosine deaminase activates a release of energy stores leading to wasting and death
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
20940317
DOI
10.1242/dmm.005389
PII: dmm.005389
Knihovny.cz E-resources
- MeSH
- Adenosine metabolism MeSH
- Adipokines metabolism MeSH
- Diet MeSH
- Drosophila melanogaster enzymology MeSH
- Energy Metabolism * MeSH
- Extracellular Space metabolism MeSH
- Phenotype MeSH
- Phosphorylase Kinase genetics metabolism MeSH
- Hemolymph metabolism MeSH
- Caloric Restriction MeSH
- Larva metabolism MeSH
- Mutation genetics MeSH
- Drosophila Proteins deficiency genetics metabolism MeSH
- Receptors, Purinergic P1 metabolism MeSH
- Carbohydrates blood MeSH
- Signal Transduction MeSH
- Suppression, Genetic MeSH
- Wasting Syndrome enzymology pathology MeSH
- Fat Body metabolism MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Adenosine MeSH
- adenosine deaminase-related growth factor, Drosophila MeSH Browser
- Adipokines MeSH
- Phosphorylase Kinase MeSH
- Drosophila Proteins MeSH
- Receptors, Purinergic P1 MeSH
- Carbohydrates MeSH
Extracellular adenosine is an important signaling molecule in neuromodulation, immunomodulation and hypoxia. Adenosine dysregulation can cause various pathologies, exemplified by a deficiency in adenosine deaminase in severe combined immunodeficiency. We have established a Drosophila model to study the effects of increased adenosine in vivo by mutating the main Drosophila adenosine deaminase-related growth factor (ADGF-A). Using a genetic screen, we show here that the increased extracellular adenosine in the adgf-a mutant is associated with hyperglycemia and impairment in energy storage. The adenosine works in this regard through the adenosine receptor as an anti-insulin hormone in parallel to adipokinetic hormone, a glucagon counterpart in flies. If not regulated properly, this action can lead to a loss of energy reserves (wasting) and death of the organism. Because adenosine signaling is associated with the immune response and the response to stress in general, our results mark extracellular adenosine as a good candidate signal involved in the wasting syndrome that accompanies various human pathologies.
References provided by Crossref.org
Extracellular adenosine mediates a systemic metabolic switch during immune response
Expression of Drosophila adenosine deaminase in immune cells during inflammatory response