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Journal of Lipid Research, Vol. 41, 940-944, June 2000
Copyright © 2000 by Lipid Research, Inc.

Original Article

Specific inhibition of rat brain phospholipase D by lysophospholipids

Correspondence to: Jiwan P. Palta

Although the importance of phospholipase D (PLD) in signal transduction in mammalian cells is well documented, the negative regulation of PLD is poorly understood. This is primarily due to a lack of known specific inhibitors of PLD. We herein report that the activity of partially purified rat brain PLD is inhibited by certain lysophospholipids, such as lysophosphatidylinositol, lysophosphatidylglycerol, and lysophosphatidylserine in a highly specific manner. Inhibition of PLD by lysophospholipids was dose-dependent: the concentration of lysophosphatidylinositol required for half-maximal inhibition was about 3 µM. An analysis of the enzyme-kinetics suggested that lysophospholipids act as non-competitive inhibitors of PLD activity. As expected, PLD activity was stimulated by ADP-ribosylation factor (Arf) and phosphatidylinositol 4,5-bisphosphate (PIP₂). The inhibition of PLD by lysophospholipids, however, was not affected by the presence or absence of Arf or by an increase in PIP₂ concentration. A protein-binding assay suggested that lysophospholipids bind directly to PLD. These results indicate that the observed inhibition of PLD by lysophospholipids is due to their direct interaction rather than to an interaction between lysophospholipids and either Arf or PIP₂.

The present study suggests that certain lysophospholipids are specific inhibitors of rat brain PLD in a cell-free system and may provide the new opportunities to investigate mechanisms by which PLD is regulated by lysophospholipids, presumably liberated by phospholipase A₂ activation, in mammalian cells.—Ryu, S. B. and J. P. Palta. Specific inhibition of rat brain phospholipase D by lysophospholipids. J. Lipid Res. 2000. 41: 940;–944.

Supplementary key words: bioactive phospholipids, PLD regulation, phospholipase A₂, LPE, LPI, LPS, LPG, LPC

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