{"title":"磷脂酶D作为神经元受体效应机制的测定","authors":"Boarder M.R., Purkiss J.R.","doi":"10.1006/ncmn.1993.1049","DOIUrl":null,"url":null,"abstract":"<div><p>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 <sup>32</sup>P-labeled neuron-like cells in culture. Alternative radiolabeling procedures, using [<sup>3</sup>H]glycerol and <sup>3</sup>H-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.</p></div>","PeriodicalId":100951,"journal":{"name":"Neuroprotocols","volume":"3 2","pages":"Pages 157-164"},"PeriodicalIF":0.0000,"publicationDate":"1993-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/ncmn.1993.1049","citationCount":"4","resultStr":"{\"title\":\"Assay of Phospholipase D as a Neuronal Receptor-Effector Mechanism\",\"authors\":\"Boarder M.R., Purkiss J.R.\",\"doi\":\"10.1006/ncmn.1993.1049\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>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 <sup>32</sup>P-labeled neuron-like cells in culture. Alternative radiolabeling procedures, using [<sup>3</sup>H]glycerol and <sup>3</sup>H-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.</p></div>\",\"PeriodicalId\":100951,\"journal\":{\"name\":\"Neuroprotocols\",\"volume\":\"3 2\",\"pages\":\"Pages 157-164\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1993-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1006/ncmn.1993.1049\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neuroprotocols\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1058674183710499\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuroprotocols","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1058674183710499","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Assay of Phospholipase D as a Neuronal Receptor-Effector Mechanism
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.