Differential response of Drosophila cell lines to extracellular adenosine
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
22266077
DOI
10.1016/j.ibmb.2012.01.002
PII: S0965-1748(12)00003-3
Knihovny.cz E-zdroje
- MeSH
- adenosin metabolismus toxicita MeSH
- adenosinkinasa antagonisté a inhibitory metabolismus MeSH
- adenosintrifosfát metabolismus MeSH
- buněčné linie MeSH
- Drosophila cytologie metabolismus MeSH
- energetický metabolismus * MeSH
- proliferace buněk MeSH
- uridin metabolismus MeSH
- viabilita buněk MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- adenosin MeSH
- adenosinkinasa MeSH
- adenosintrifosfát MeSH
- uridin 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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