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Adenosine Receptor and Its Downstream Targets, Mod(mdg4) and Hsp70, Work as a Signaling Pathway Modulating Cytotoxic Damage in Drosophila
- Source :
- Frontiers in Cell and Developmental Biology, Vol 9 (2021), Frontiers in Cell and Developmental Biology
- Publication Year :
- 2021
- Publisher :
- Frontiers Media S.A., 2021.
-
Abstract
- SummaryAdenosine (Ado) is an important signaling molecule involved in stress responses. Studies in mammalian models have shown that Ado regulates signaling mechanisms involved in ‘danger-sensing’ and tissue-protection. Yet, little is known about the role of Ado signaling inDrosophila. In the present study, we observed lower extracellular Ado concentration and suppressed expression of Ado transporters in flies expressing mutant huntingtin protein (mHTT). We altered Ado signaling using genetic tools and found that the overexpression of Ado metabolic enzymes, as well as the suppression of Ado receptor (AdoR) and transporters (ENTs), were able to minimize mHTT-induced mortality. We also identified the downstream targets of the AdoR pathway, the modifier of mdg4 (Mod(mdg4)) and heat-shock protein 70 (Hsp70), which carry out its function. Finally, we showed that a decrease in Ado signaling affect otherDrosophilastress reactions, including paraquat and heat-shock treatments. Our study provides important insights into how Ado regulates stress responses inDrosophila.
- Subjects :
- Mutant
heat-shock protein 70
Cell and Developmental Biology
modifier of mdg4
Extracellular
medicine
Huntingtin Protein
Receptor
lcsh:QH301-705.5
Original Research
Chemistry
Neurodegeneration
mutant huntingtin
neurodegeneration
Equilibrative nucleoside transporter
Transporter
Cell Biology
medicine.disease
Adenosine
Adenosine receptor
Cell biology
lcsh:Biology (General)
equilibrative nucleoside transporter
cytotoxicity
Signal transduction
Developmental Biology
medicine.drug
Subjects
Details
- Language :
- English
- Volume :
- 9
- Database :
- OpenAIRE
- Journal :
- Frontiers in Cell and Developmental Biology
- Accession number :
- edsair.doi.dedup.....8c61bfbf9264f7f1f0beba209da45b46
- Full Text :
- https://doi.org/10.3389/fcell.2021.651367/full