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Insulin secretion by 'kiss-and-run' exocytosis in clonal pancreatic islet beta-cells.

Abstract
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 beta-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.
AuthorsT Tsuboi, G A Rutter
JournalBiochemical Society transactions (Biochem Soc Trans) Vol. 31 Issue Pt 4 Pg. 833-6 (Aug 2003) ISSN: 0300-5127 [Print] England
PMID12887316 (Publication Type: Journal Article, Review)
Chemical References
  • Calcium-Binding Proteins
  • Insulin
  • Luminescent Proteins
  • Membrane Glycoproteins
  • Nerve Tissue Proteins
  • Neuropeptide Y
  • SYT4 protein, human
  • Synaptotagmins
Topics
  • Animals
  • Calcium-Binding Proteins
  • Clone Cells
  • Exocytosis (physiology)
  • Humans
  • Insulin (metabolism)
  • Insulin Secretion
  • Islets of Langerhans (cytology, metabolism)
  • Luminescent Proteins (metabolism)
  • Membrane Fusion (physiology)
  • Membrane Glycoproteins (metabolism)
  • Microscopy, Fluorescence (methods)
  • Nerve Tissue Proteins (metabolism)
  • Neuropeptide Y (metabolism)
  • Secretory Vesicles (physiology)
  • Synaptotagmins

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