Levitan E S
Department of Pharmacology, University of Pittsburgh, Pittsburgh, Pennsylvania, 15261, USA.
Methods. 1998 Oct;16(2):182-7. doi: 10.1006/meth.1998.0665.
Neurons and endocrine cells release peptides stored in a limited pool of secretory granules. Although it has been possible to measure secretion or exocytosis, studying events within cells that influence the size and speed of secretory responses has been difficult. Here we describe how green fluorescent protein (GFP)-tagged hormones can be used to measure release and granule mobility. Epifluorescence allows one to measure total peptide content and granule trajectories within a plane of focus. Confocal microscopy facilitates measurements within a better defined optical section. Granule mobility can also be measured with fluorescence recovery after photobleaching (FRAP). Application of these optical approaches to the study of neuronal peptide secretion has revealed that the releasable pool is not spatially defined and that sustained peptide release is limited by the availability of mobile secretory granules.
神经元和内分泌细胞释放储存在有限分泌颗粒池中的肽。虽然已经能够测量分泌或胞吐作用,但研究细胞内影响分泌反应大小和速度的事件一直很困难。在这里,我们描述了如何使用绿色荧光蛋白(GFP)标记的激素来测量释放和颗粒移动性。落射荧光使人们能够测量聚焦平面内的总肽含量和颗粒轨迹。共聚焦显微镜有助于在定义更清晰的光学切片内进行测量。颗粒移动性也可以用光漂白后的荧光恢复(FRAP)来测量。将这些光学方法应用于神经元肽分泌的研究表明,可释放池在空间上没有明确界定,并且持续的肽释放受到可移动分泌颗粒可用性的限制。