2003Humana Press eBooksRequires access

The Measurement of Phospholipase D-Linked Signaling in Cells

Michael J.O. Wakelam, Matthew N. Hodgkin, Ashley Martin

Open publisher page 23 citations

Abstract

There is now increasing evidence that phospholipase D (PLD) activity can be stimulated by a range of hormones, growth factors, and neurotransmitters in a range of cell types ( 1 ). The enzyme generally catalyzes the hydrolysis of phosphatidylcholine (PtdCho) to produce phosphatidate (PtdOH) and choline (Cho), although the hydrolysis of phosphatidylethanolamine has been reported. PtdOH can be converted to diacylglycerol (DAG) by the action of phosphatidate phosphohydrolase, and the PLD pathway has thus been suggested to provide a source of DAG in cells. This reaction clearly takes place, however, whether it provides a DAG, which has a signaling function, remains unclear. This chapter describes methods to determine PLD activity and also to examine the levels of both PtdOH and DAG. These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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What this paper is about

There is now increasing evidence that phospholipase D (PLD) activity can be stimulated by a range of hormones, growth factors, and neurotransmitters in a range of cell types ( 1 ). The enzyme generally catalyzes the hydrolysis of phosphatidylcholine (PtdCho) to produce phosphatidate (PtdOH) and choline (Cho), although the hydrolysis of phosphatidylethanolamine has been reported. PtdOH can be converted to diacylglycerol (DAG) by the action of phosphatidate phosphohydrolase, and the PLD pathway has thus been suggested to provide a source of DAG in cells. This reaction clearly takes place, however, whether it provides a DAG, which has a signaling function, remains unclear. This chapter describes methods to determine PLD activity and also to examine the levels of both PtdOH and DAG. These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Available abstract

There is now increasing evidence that phospholipase D (PLD) activity can be stimulated by a range of hormones, growth factors, and neurotransmitters in a range of cell types ( 1 ). The enzyme generally catalyzes the hydrolysis of phosphatidylcholine (PtdCho) to produce phosphatidate (PtdOH) and choline (Cho), although the hydrolysis of phosphatidylethanolamine has been reported. PtdOH can be converted to diacylglycerol (DAG) by the action of phosphatidate phosphohydrolase, and the PLD pathway has thus been suggested to provide a source of DAG in cells. This reaction clearly takes place, however, whether it provides a DAG, which has a signaling function, remains unclear. This chapter describes methods to determine PLD activity and also to examine the levels of both PtdOH and DAG. These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Key concepts: Phosphatidate, Phospholipase D, Diacylglycerol kinase, Phosphatidylethanolamine, Phosphatidic acid, Phosphatidylcholine, Phospholipase, Biochemistry

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