Prostaglandin E1 inhibits endocytosis in the β-cell endocytosis

Author:

Zhao Ying123,Fang Qinghua23,Straub Susanne G1,Lindau Manfred23,Sharp Geoffrey W G1

Affiliation:

1. 1Department of Molecular MedicineCornell University, Ithaca, New York, USA

2. 2School of Applied and Engineering PhysicsCornell University, Ithaca, New York, USA

3. 3Laboratory for Nanoscale Cell BiologyMax-Planck-Institute for Biophysical Chemistry, Goettingen, Germany

Abstract

Prostaglandins inhibit insulin secretion in a manner similar to that of norepinephrine (NE) and somatostatin. As NE inhibits endocytosis as well as exocytosis, we have now examined the modulation of endocytosis by prostaglandin E1 (PGE1). Endocytosis following exocytosis was recorded by whole-cell patch clamp capacitance measurements in INS-832/13 cells. Prolonged depolarizing pulses producing a high level of Ca2+ influx were used to stimulate maximal exocytosis and to deplete the readily releasable pool (RRP) of granules. This high Ca2+ influx eliminates the inhibitory effect of PGE1 on exocytosis and allows specific characterization of the inhibitory effect of PGE1 on the subsequent compensatory endocytosis. After stimulating exocytosis, endocytosis was apparent under control conditions but was inhibited by PGE1 in a Pertussis toxin-sensitive (PTX)-insensitive manner. Dialyzing a synthetic peptide mimicking the C-terminus of the α-subunit of the heterotrimeric G-protein Gz into the cells blocked the inhibition of endocytosis by PGE1, whereas a control-randomized peptide was without effect. These results demonstrate that PGE1 inhibits endocytosis and Gz mediates the inhibition.

Publisher

Bioscientifica

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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