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A direct method for the simultaneous measurement of ceramide and phospholipase D activity.

作者信息

Liu G, Kleine L, Hébert R L

机构信息

Department of Cellular and Molecular Medicine, Kidney Research Center, University of Ottawa, Ottawa, ON K1H 8M5, Canada.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 2000 Oct;63(4):187-94. doi: 10.1054/plef.2000.0205.

DOI:10.1054/plef.2000.0205
PMID:11049693
Abstract

Both ceramide and phospholipase D (PLD) have important roles in a variety of signal transduction pathways. Recent evidence suggests that ceramide is a novel second messenger with specific biological effects. Publications in this field have increased rapidly in the last few years. However, a method to directly and rapidly measure cermide production has been lacking. Herein, we report on a novel, inexpensive, direct and rapid assay for the measurement of ceramide and the simultaneous measurement of PLD activity. This method uses labeling of cells with [(14)C]myristic acid and a TLC solvent of ethyl acetate/acetic acid/trimethylpentane. This method avoids the loss of radioactivity and variability due to changes in DAG kinase activity that are associated with the commonly-used DAG kinase assay.

摘要

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