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Updated: Aug 11, 2026

Imaging FITC-dextran as a Reporter for Regulated Exocytosis
Published on: June 20, 2018
Regulation of dense core release from neuroendocrine cells revealed by imaging single exocytic events
J K Angleson1, A J Cochilla, G Kilic
1Department of Physiology and Biophysics, University of Colorado Medical School, Denver 80262, USA.
Abstract:
Using FM1-43 fluorescence, we have optically detected single exocytic and endocytic events in rat pituitary lactotrophs. About fifty discrete fluorescent spots abruptly appear around the entire surface of a cell bathed in FM1-43 and high-potassium saline. The spots, which also immunostain for prolactin, reflect the labeling of dense cores as well as membranes of exocytosed secretory granules. Stained cores are not released, but remain attached to the cell and are eventually endocytosed. However, in cells exposed to dopamine (or an analog, bromocriptine), the cores dissolve and are secreted after several seconds. Solubilization of dense cores is mediated through a reduction in cytoplasmic cyclic AMP. Thus, the composition of secretions from individual secretory granules is regulated.
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