Korean J Physiol Pharmacol.
2001 Apr;5(2):139-146.
Modulation of L-type Ca2+ channel currents by various protein kinase
activators and inhibitors in rat clonal pituitary GH3 cell line
- Affiliations
-
- 1Department of Physiology, Seoul National University College of
Medicine, 28 Yeongeon-dong, Jongno-gu, Seoul, South Korea.
wonkyung@snu.ac.kr
Abstract
- L-type Ca2+ channels play an important role in regulating cytosolic
Ca2+ and thereby regulating hormone secretions in neuroendocrine cells.
Since hormone secretions are also regulated by various kinds of protein
kinases, we investigated the role of some kinase activators and
inhibitors in the regulation of the L-type Ca2+ channel currents in rat
pituitary GH3 cells using the patch-clamp technique. Phorbol
12,13-dibutyrate (PDBu), a protein kinase C (PKC) activator, and
vanadate, a protein tyrosine phosphatase (PTP) inhibitor, increased the
Ba2+ current through the L-type Ca2+ channels. In contrast,
bisindolylmaleimide I (BIM I), a PKC inhibitor, and genistein, a
protein tyrosine kinase (PTK) inhibitor, suppressed the Ba2+ currents.
Forskolin, an adenylate cyclase activator, and isobutyl methylxanthine
(IBMX), a non-specific phosphodiesterase inhibitor, reduced Ba2+
currents. The above results show that the L-type Ca2+ channels are
activated by PKC and PTK, and inhibited by elevation of cyclic
nucleotides such as cAMP. From these results, it is suggested that the
regulation of hormone secretion by various kinase activity in GH3 cells
may be attributable, at least in part, to their effect on L-type Ca2+
channels.