Arachidonic acid and lysophosphatidylcholine inhibit multiple late steps of regulated exocytosis

Abstract

The canonical Phospholipase A₂ (PLA₂) metabolites lysophosphatidylcholine (LPC) and arachidonic acid (ARA) affect regulated exocytosis in a wide variety of cells and are proposed to directly influence membrane merger owing to their respective spontaneous curvatures. According to the Stalk-pore hypothesis, negative curvature ARA inhibits and promotes bilayer merger upon introduction into the distal or proximal monolayers, respectively; in contrast, with positive curvature, LPC has the opposite effects. Using fully primed, release-ready native cortical secretory vesicles (CV), well-established fusion assays and standardized lipid analyses, we show that exogenous ARA and LPC, as well as their non-metabolizable analogous, ETYA and ET-18-OCH3, inhibit the docking/priming and membrane merger steps, respectively, of regulated exocytosis.

Keywords: Arachidonic acid; ET-18-OCH3; ETYA; Lysophosphatidylcholine; Native membrane fusion; Phospholipase A(2).