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Voltage-dependent phosphorylation may recruit Ca2+ current facilitation in chromaffin cells.
- Source :
-
Nature [Nature] 1992 Jul 02; Vol. 358 (6381), pp. 63-6. - Publication Year :
- 1992
-
Abstract
- Bovine chromaffin cells have two components of whole-cell Ca2+ current: 'standard' Ca2+ currents that are activated by brief depolarizations, and 'facilitation' Ca2+ currents, which are normally quiescent but can be activated by large pre-depolarizations or by repetitive depolarizations to physiological potentials. The activation of protein kinase A can also stimulate Ca2+ current facilitation, indicating that phosphorylation can play a part in facilitation. Here we investigate the role of protein phosphorylation in the recruitment of facilitation Ca2+ currents by pre-pulses or repetitive depolarizations. We find that recruitment of facilitation by depolarization is a rapid first-order process which is suppressed by inhibitors of protein phosphorylation or by injection of phosphatase 2A into cells. Recruitment of facilitation Ca2+ current by voltage is normally reversible but phosphatase inhibitors render it irreversible. Our results indicate that recruitment of these Ca2+ currents by pre-pulses or repetitive depolarizations involves voltage-dependent phosphorylation of the facilitation Ca2+ channel or a closely associated regulatory protein. Voltage-dependent phosphorylation may therefore be a mechanism by which membrane potential can modulate ion channel activity.
- Subjects :
- 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
Adenosine Triphosphate metabolism
Animals
Cattle
Ethers, Cyclic pharmacology
In Vitro Techniques
Ion Channel Gating
Isoquinolines pharmacology
Membrane Potentials
Okadaic Acid
Phosphoprotein Phosphatases antagonists & inhibitors
Phosphorylation
Piperazines pharmacology
Protein Kinase Inhibitors
Protein Phosphatase 2
Adrenal Medulla physiology
Calcium physiology
Calcium Channels physiology
Subjects
Details
- Language :
- English
- ISSN :
- 0028-0836
- Volume :
- 358
- Issue :
- 6381
- Database :
- MEDLINE
- Journal :
- Nature
- Publication Type :
- Academic Journal
- Accession number :
- 1319555
- Full Text :
- https://doi.org/10.1038/358063a0