Exocytotic release of neuropeptides and hormones is generally believed to involve the complete merger of the secretory vesicle with the plasma membrane. However, recent data have suggested that ‘kiss-and-run’ mechanisms may also play a role. To analyse secretory events in neuroendocrine β-cells, we imaged chimaeric reporters targeted to either the vesicle membrane [chimaeras of synaptobrevin-2 and pH-sensitive green fluorescent protein (synapto·pHluorin) or of phogrin (phosphatase on the granule of insulinoma) and enhanced green fluorescent protein (EGFP) (phogrin·EGFP)] or the lumen [neuropeptide Y (NPY)·pH-insensitive yellow fluorescent protein (Venus)] by evanescent wave microscopy. Unexpectedly, the frequency of NPY·Venus release events was only 17–27% of that of vesicle fusion reported with synapto·pHluorin, but not phogrin·EGFP, indicating that exocytosis of cargo peptides that is likely to require complete collapse of the vesicle into the plasma membrane is relatively rare. However, both the frequency and the kinetics of NPY·Venus release were modulated by stimulus strength or by overexpression of synaptotagmin IV, demonstrating the plasticity of ‘kiss-and-run’ fusion.
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Conference Article| August 01 2003
Insulin secretion by ‘kiss-and-run’ exocytosis in clonal pancreatic islet β-cells
G.A. Rutter 1
Henry Wellcome Laboratories for Integrated Cell Signalling and Department of Biochemistry, School of Medical Sciences, University Walk, University of Bristol, Bristol BS8 1TD, U.K.
1To whom correspondence should be addressed (e-mail email@example.com).
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Biochem Soc Trans (2003) 31 (4): 833–836.
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T. Tsuboi, G.A. Rutter; Insulin secretion by ‘kiss-and-run’ exocytosis in clonal pancreatic islet β-cells. Biochem Soc Trans 1 August 2003; 31 (4): 833–836. doi: https://doi.org/10.1042/bst0310833
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