Hepoxilins and trioxilins in barnacles: an analysis of their potential roles in egg hatching and larval settlement
Author:
Vogan Claire L.1, Maskrey Ben H.1, Taylor Graham W.2, Henry Sheelagh3, Pace-Asciak Cecil R.4, Clare Anthony S.3, Rowley Andrew F.1
Affiliation:
1. School of Biological Sciences, University of Wales Swansea, Singleton Park, Swansea, SA2 8PP, UK 2. Proteomics Section, Imperial College, Faculty of Medicine, London, W12 ONN, UK 3. School of Marine Science and Technology, University of Newcastle upon Tyne, Newcastle upon Tyne, NE1 7RU, UK 4. Program in Integrative Biology, Research Institute, The Hospital for Sick Children, 555-University Avenue, Toronto and the Department of Pharmacology,University of Toronto, Toronto, Ontario M5G 1X8, Canada
Abstract
SUMMARY
The barnacle life cycle has two key stages at which eicosanoids are believed to be involved in cellular communication pathways, namely the hatching of nauplii and the settlement of cypris larvae. Barnacle egg-hatching activity has previously been reported to reside in a variety of eicosanoids,including 8-hydroxyeicosapentaenoic acid and a number of tri-hydroxylated polyunsaturated fatty acid derivatives, the trioxilins. The production of the eicosapentaenoic acid metabolite trioxilin A4(8,11,12-trihydroxy-5,9,14,17-eicosatetraenoic acid) by the barnacles Balanus amphitrite and Elminius modestus was confirmed using a combination of high-performance liquid chromatography and gas chromatography, both linked to mass spectrometry. In addition, both species also generated trioxilin A3(8,11,12-trihydroxy-5,9,14-eicosatrienoic acid; an arachidonic acid-derived product), 8,11,12-trihydroxy-9,14,17-eicosatrienoic acid (a ω3 analogue of trioxilin A3; derived from ω3 arachidonic acid) and 10,13,14-trihydroxy-4,7,11,16,19-docosapentaenoic acid (a docosahexaenoic acid-derived product). In contrast to earlier reports, trioxilin A3had no E. modestus egg-hatching activity at any of the concentrations tested (10–9–10–6 mol l–1). The unstable epoxide precursor hepoxilin A3,however, caused significant levels of hatching at 10–6 mol l–1. Furthermore, the stable hepoxilin B3 analogue PBT-3 stimulated hatching at 10–7 mol l–1. Neither trioxilin A3, hepoxilin A3 or PBT-3 at 0.25–30 μmol l–1 served as settlement cues for B. amphitrite cypris larvae.
Publisher
The Company of Biologists
Subject
Insect Science,Molecular Biology,Animal Science and Zoology,Aquatic Science,Physiology,Ecology, Evolution, Behavior and Systematics
Reference28 articles.
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