Functional characterization of eicosanoid signaling in Drosophila development

preprint OA: closed
📄 Open PDF Full text JSON View at publisher
Full text 2,892 characters · extracted from oa-doi-fallback · click to expand
Abstract 20-carbon fatty acid-derived eicosanoids are versatile signaling oxylipins in mammals. In particular, a group of eicosanoids termed prostanoids are involved in multiple physiological processes, such as reproduction and immune responses. Although some eicosanoids such as prostaglandin E2 (PGE2) have been detected in some insect species, molecular mechanisms of eicosanoid synthesis and signal transduction in insects have not been thoroughly investigated. Our phylogenetic analysis indicated that, in clear contrast to the presence of numerous receptors for oxylipins and other lipid mediators in humans, the Drosophila genome only possesses a single ortholog of such receptors, which is homologous to human prostanoid receptors. This G protein-coupled receptor, named Prostaglandin Receptor or PGR, is activated by PGE2 and its isomer PGD2 in Drosophila S2 cells. PGR mutant flies die as pharate adults with insufficient tracheal development, which can be rescued by supplying high oxygen. Consistent with this, through a comprehensive mutagenesis approach, we identified a Drosophila PGE synthase whose mutants show similar pharate adult lethality with hypoxia responses. Drosophila thus has a highly simplified eicosanoid signaling pathway as compared to humans, and it may provide an ideal model system for investigating evolutionarily conserved aspects of eicosanoid signaling. Author Summary There are numerous bioactive lipids that control animal physiology, and some of them are commonly observed in both humans and insects. Well-studied insects such as fruit flies can therefore be an excellent gateway to learn about lipid molecules that have common functions in various animal species. In this study, we analyzed the fruit fly genome to look for genes that encode sensors (or receptors) for such lipid molecules called lipid mediators and found that the fruit fly only has one such receptor, as compared to ∼50 receptors in humans. Interestingly, the fly receptor we found was similar to human receptors for lipid molecules called prostanoids. Our work on the fruit fly prostanoid receptor further revealed that it is important for development of the fly respiratory system, and we showed that flies can also synthesize prostanoids in their body just like humans. Prostanoids are clinically important due to their pro-inflammatory functions, and some widely used drugs such as ibuprofen target enzymes that synthesize prostanoids. Our study on fruit fly prostanoids therefore provides a solid basis for using this simple organism to reveal common prostanoid functions in animals, which may provide important insights into animal health in general. Competing Interest Statement The authors have declared no competing interest. Footnotes Expression analysis of the PGR-Gal4 line was updated in Figure 2 and S3 Figure, along with some other minor changes and clarifications.

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2025) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

europepmc
last seen: 2026-05-20T01:45:00.602351+00:00