TEMPORAL AND SPATIAL MONITORING OF EXOCYTOSIS WITH NATIVE FLUORESCENCE IMAGING MICROSCOPY

Citation
Sj. Lillard et Es. Yeung, TEMPORAL AND SPATIAL MONITORING OF EXOCYTOSIS WITH NATIVE FLUORESCENCE IMAGING MICROSCOPY, Journal of neuroscience methods, 75(1), 1997, pp. 103-109
Citations number
18
Categorie Soggetti
Neurosciences
ISSN journal
01650270
Volume
75
Issue
1
Year of publication
1997
Pages
103 - 109
Database
ISI
SICI code
0165-0270(1997)75:1<103:TASMOE>2.0.ZU;2-6
Abstract
Exocytosis of rat peritoneal mast cells (RPMCs) was monitored temporal ly and spatially using native fluorescence imaging microscopy with 305 -nm laser excitation. Real time chemical images of the relative amount s of serotonin and protein released from each cell are obtained, Indiv idual cells released different amounts of material and the time delay of the release event after stimulation by polymyxin varied from cell t o cell. Release consisted of a main burst of activity followed by slow sustained secretion over many seconds. The images show that different regions of a given cell behave asynchronously in releasing material i nto the surrounding medium. On rare occasions, highly localized fluore scence bursts can be seen in the vicinity of the cell. Presumably, the se are due to delayed release of fluorescent mediators from single gra nules, following detachment of the latter from the cell. These quantit ative fluorescence measurements allow one to follow the time-course of the physiologically important parameter---the amount of material that is secreted into the body fluid on stimulation. (C) 1997 Elsevier Sci ence B.V.