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Erik Renström

Erik Renström

Vice-chancellor

Erik Renström

Fast exocytosis with few Ca(2+) channels in insulin-secreting mouse pancreatic B cells

Author

  • Sebastian Barg
  • Xiaosong Ma
  • Lena Eliasson
  • Juris Galvanovskis
  • Sven Göpel
  • Stefanie Obermüller
  • Josef Platzer
  • Erik Renström
  • Michel Trus
  • Daphne Atlas
  • Jörg Striessnig
  • Patrik Rorsman

Summary, in English

The association of L-type Ca(2+) channels to the secretory granules and its functional significance to secretion was investigated in mouse pancreatic B cells. Nonstationary fluctuation analysis showed that the B cell is equipped with <500 alpha1(C) L-type Ca(2+) channels, corresponding to a Ca(2+) channel density of 0.9 channels per microm(2). Analysis of the kinetics of exocytosis during voltage-clamp depolarizations revealed an early component that reached a peak rate of 1.1 pFs(-1) (approximately 650 granules/s) 25 ms after onset of the pulse and is completed within approximately 100 ms. This component represents a subset of approximately 60 granules situated in the immediate vicinity of the L-type Ca(2+) channels, corresponding to approximately 10% of the readily releasable pool of granules. Experiments involving photorelease of caged Ca(2+) revealed that the rate of exocytosis was half-maximal at a cytoplasmic Ca(2+) concentration of 17 microM, and concentrations >25 microM are required to attain the rate of exocytosis observed during voltage-clamp depolarizations. The rapid component of exocytosis was not affected by inclusion of millimolar concentrations of the Ca(2+) buffer EGTA but abolished by addition of exogenous L(C753-893), the 140 amino acids of the cytoplasmic loop connecting the 2(nd) and 3(rd) transmembrane region of the alpha1(C) L-type Ca(2+) channel, which has been proposed to tether the Ca(2+) channels to the secretory granules. In keeping with the idea that secretion is determined by Ca(2+) influx through individual Ca(2+) channels, exocytosis triggered by brief (15 ms) depolarizations was enhanced 2.5-fold by the Ca(2+) channel agonist BayK8644 and 3.5-fold by elevating extracellular Ca(2+) from 2.6 to 10 mM. Recordings of single Ca(2+) channel activity revealed that patches predominantly contained no channels or many active channels. We propose that several Ca(2+) channels associate with a single granule thus forming a functional unit. This arrangement is important in a cell with few Ca(2+) channels as it ensures maximum usage of the Ca(2+) entering the cell while minimizing the influence of stochastic variations of the Ca(2+) channel activity.

Department/s

  • Islet cell physiology
  • Department of Experimental Medical Science
  • Diabetes - Islet Cell Exocytosis
  • Department of Clinical Sciences, Malmö

Publishing year

2001

Language

English

Pages

3308-3323

Publication/Series

Biophysical Journal

Volume

81

Issue

6

Document type

Journal article

Publisher

Cell Press

Topic

  • Biophysics

Status

Published

Research group

  • Islet cell physiology
  • Diabetes - Islet Cell Exocytosis

ISBN/ISSN/Other

  • ISSN: 1542-0086