Differential response of Drosophila cell lines to extracellular adenosine
Language English Country England, Great Britain Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
22266077
DOI
10.1016/j.ibmb.2012.01.002
PII: S0965-1748(12)00003-3
Knihovny.cz E-resources
- MeSH
- Adenosine metabolism toxicity MeSH
- Adenosine Kinase antagonists & inhibitors metabolism MeSH
- Adenosine Triphosphate metabolism MeSH
- Cell Line MeSH
- Drosophila cytology metabolism MeSH
- Energy Metabolism * MeSH
- Cell Proliferation MeSH
- Uridine metabolism MeSH
- Cell Survival MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Adenosine MeSH
- Adenosine Kinase MeSH
- Adenosine Triphosphate MeSH
- Uridine MeSH
Adenosine (Ado) is a crucial metabolite that affects a wide range of physiological processes. Key proteins regulating Ado signaling, transport and metabolism are conserved among vertebrates and invertebrates. It is well known that Ado influences proliferation of several vertebrate and invertebrate cells. Here we show that Ado negatively influences viability, changes morphology and mitochondrial polarity of the Drosophila imaginal disc cell line (Cl.8+) via a mechanism exclusively dependent on cellular Ado uptake. High transport of Ado is followed by phosphorylation and ATP production as a part of Ado salvation, which at higher concentrations may interfere with cellular homeostasis. In contrast, hematopoietic cell line Mbn2, which grows well in high Ado concentration, preferentially uses adenosine deaminase as a part of the purine catabolic pathway. Our results show that different types of Drosophila cell lines use different pathways for Ado conversion and suggest that such differences may be an important part of complex mechanisms maintaining energy homeostasis in the body.
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