{"title":"Assay of Phospholipase D as a Neuronal Receptor-Effector Mechanism","authors":"M. Boarder, J. Purkiss","doi":"10.1006/NCMN.1993.1049","DOIUrl":null,"url":null,"abstract":"Abstract Phospholipase D is a commonly encountered but poorly understood member of the phospholipase family of cell signaling enzymes. Until recently, its study was inhibited by the lack of a simple and adaptable assay in intact cells that is not complicated by the presence of phospholipase C activity. Here, we review the various methods used to measure phospholipase D in whole cells in culture and with disrupted neuronal preparations, and we introduce the use of transphosphatidylation as a method of measuring the activity of phospholipase D in the presence of millimolar concentrations of alcohol. We then describe in detail the use of transphosphatidylation by butanol with 32P-labeled neuron-like cells in culture. Alternative radiolabeling procedures, using [3H]glycerol and 3H-labeled fatty acids, with these cells are discussed. Finally, the application of procedures such as these to brain preparations, in particular, to intact synaptosomal preparations, is described.","PeriodicalId":100951,"journal":{"name":"Neuroprotocols","volume":"22 1","pages":"157-164"},"PeriodicalIF":0.0000,"publicationDate":"1993-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuroprotocols","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1006/NCMN.1993.1049","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4
Abstract
Abstract Phospholipase D is a commonly encountered but poorly understood member of the phospholipase family of cell signaling enzymes. Until recently, its study was inhibited by the lack of a simple and adaptable assay in intact cells that is not complicated by the presence of phospholipase C activity. Here, we review the various methods used to measure phospholipase D in whole cells in culture and with disrupted neuronal preparations, and we introduce the use of transphosphatidylation as a method of measuring the activity of phospholipase D in the presence of millimolar concentrations of alcohol. We then describe in detail the use of transphosphatidylation by butanol with 32P-labeled neuron-like cells in culture. Alternative radiolabeling procedures, using [3H]glycerol and 3H-labeled fatty acids, with these cells are discussed. Finally, the application of procedures such as these to brain preparations, in particular, to intact synaptosomal preparations, is described.