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
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.