Assay of Phospholipase D as a Neuronal Receptor-Effector Mechanism

M. Boarder, J. Purkiss
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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.
磷脂酶D作为神经元受体-效应机制的研究
磷脂酶D是细胞信号酶的磷脂酶家族中一个常见但了解甚少的成员。直到最近,由于缺乏一种在完整细胞中不因磷脂酶C活性的存在而复杂化的简单且适应性强的测定,其研究受到抑制。在这里,我们回顾了在培养的全细胞和破坏的神经元制剂中测量磷脂酶D的各种方法,并介绍了在毫摩尔浓度的酒精存在下使用转磷脂酰化作为测量磷脂酶D活性的方法。然后,我们详细描述了在培养中使用丁醇转磷脂酰化32p标记的神经元样细胞。讨论了使用[3H]甘油和3H标记脂肪酸的替代放射性标记程序。最后,程序的应用,如这些脑准备,特别是完整的突触体准备,描述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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