Interaction between eicosanoids and the complement system in salmonid fish

Dev Comp Immunol. 2012 Jan;36(1):1-9. doi: 10.1016/j.dci.2011.05.007. Epub 2011 Jun 1.

Abstract

Both eicosanoid generation and the complement system have long evolutionary histories predating the emergence of the vertebrates over 500 myr ago. This study investigated the interplay between these two systems in an example of a bony fish, the rainbow trout (Oncorhynchus mykiss). Specifically, it examined whether purified complement fragments including C3a-1 and zymosan-activated serum, stimulate the biosynthesis of any of these eicosanoids by trout macrophages. Incubation of macrophages with zymosan pre-incubated with normal trout serum resulted in the phagocytosis of such particles and the generation of both intra- and extra-cellularly located lipoxygenase and cyclooxygenase products. Both eicosanoid generation and phagocytosis levels were significantly elevated following incubation of zymosan in trout serum in comparison with heat-inactivated (60°C for 30 min) trout serum and saline alone. A combined mass spectrometry/high performance liquid chromatography approach was employed to conclusively demonstrate the presence of the cyclooxygenase product, prostaglandin E (PGE) in the culture supernatants of ionophore-challenged macrophages. Incubation of trout macrophages with zymosan-activated trout serum (i.e. no zymosan present) failed to stimulate PGE generation. Similarly, incubation of these cells for up to 60 min with C3a-1 (4 or 50 nM) failed to generate significant amounts of PGE or lipoxygenase products such as leukotriene B(4/5) or lipoxin A(4/5). Longer term (6 & 24h) incubation of macrophages with C3a-1 (4 nM) resulted in a time dependent increase in the generation of PGE but not leukotriene B in culture supernatants. No conclusive evidence that the increase in PGE generation was caused by changes in the expression of either cyclooxygenase-1 or -2 was found.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cells, Cultured
  • Chromatography, High Pressure Liquid
  • Complement C3a / immunology
  • Complement C3a / metabolism*
  • Complement Pathway, Alternative
  • Fish Proteins / immunology
  • Fish Proteins / metabolism*
  • Gene Expression Regulation / immunology
  • Lipoxygenase / genetics
  • Lipoxygenase / immunology
  • Lipoxygenase / metabolism
  • Macrophages / immunology
  • Macrophages / metabolism*
  • Macrophages / pathology
  • Mass Spectrometry
  • Oncorhynchus mykiss* / immunology
  • Phagocytosis / immunology
  • Prostaglandin-Endoperoxide Synthases / genetics
  • Prostaglandin-Endoperoxide Synthases / immunology
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Prostaglandins E / metabolism*
  • Zymosan / immunology
  • Zymosan / metabolism

Substances

  • Fish Proteins
  • Prostaglandins E
  • Complement C3a
  • Zymosan
  • Lipoxygenase
  • Prostaglandin-Endoperoxide Synthases