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B Hellman

Publications and source records attributed to B Hellman.

273 records · Page 16Linked to original sources

Activation of G-proteins induces Ca2+ oscillations with hyperpolarizing K+ currents in pancreatic beta-cells.

Activation of G-proteins by internal perfusion with GTP-gamma-S or external application of carbachol resulted in oscillations of cytoplasmic Ca2+ in isolated mouse pancreatic beta-cells. The Ca2+ transients were associated with the generation of K+ currents sufficiently pronounced to induce marked pulses of hyperpolarization. The oscillatory G-protein response remained largely unaffected when altering the membrane potential. The oscillations became less frequent in the presence of 1 mM neomycin and disappeared when the cells were internally perfused with 100 micrograms/ml heparin. The frequency of the oscillations was positively correlated with the basal level of cytoplasmic Ca2+. Addition of Ca2+ to the internal perfusion medium increased the oscillatory rate and buffering of the ion with Indo-1 or EGTA had the opposite effect. It is concluded that G-protein activation results in cyclic mobilisation of intracellular calcium mediated by inositol-1,4,5-triphosphate and that the basal concentration of cytoplasmic Ca2+ is an important determinant for the frequency of the oscillations.

Animals↗

The role of Ca2+ in the release of pancreatic islet hormones.

The role of Ca2+ in initiating exocytosis of granule-bound secretory products was evaluated with respect to pancreatic islet hormones. Apart from stimulating the transfer of the granules to the plasma membrane and their subsequent extrusion, a rise of the cytoplasmic Ca2+ concentration ([Ca2+]i) may under certain conditions also have depressive effects on insulin release. Glucose has a bidirectional action on [Ca2+]i by stimulating both the entry of the ion and its removal by organelle sequestration and outward transport. The recognition of glucose as a secretory stimulus is based on sudden transitions between oscillatory and steady-state [Ca2+]i at threshold concentrations of the sugar characteristic for the individual beta-cell. The intrinsic ability of each beta-cell to generate oscillations of [Ca2+]i and the subsequent synchronization of these signals result in a pulsatile release of insulin from isolated islets. Glucose regulation of this process is manifested as alterations of the amplitudes of the insulin pulses without effects on the frequency. It is suggested that electrical signalling from the beta-cells in combination with direct effects of glucose are important for regulating the release of glucagon and somatostatin.

Animals↗