Molecular diversity of voltage-dependent Ca2+ channels

Voltage-dependent Ca2+ channels regulate Ca2+ entry and thereby contribute to Ca2+ signalling in many cells. Functional studies have uncovered several types of Ca2+ channel, distinguished by pharmacology, electrophysiology and tissue localization. More recently, molecular cloning has revealed an eve...

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Veröffentlicht in:Trends in pharmacological sciences (Regular ed.) 1991-09, Vol.12 (9), p.349-354
Hauptverfasser: Tsien, R W, Ellinor, P T, Horne, W A
Format: Artikel
Sprache:eng
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Zusammenfassung:Voltage-dependent Ca2+ channels regulate Ca2+ entry and thereby contribute to Ca2+ signalling in many cells. Functional studies have uncovered several types of Ca2+ channel, distinguished by pharmacology, electrophysiology and tissue localization. More recently, molecular cloning has revealed an even greater diversity among Ca2+ channels, arising from multiple genes and alternative splicing. L-type, dihydropyridine-sensitive Ca2+ channels have been the most extensively characterized to date. Recently, Numa's group has reported the cloning and expression of a dihydropyridine-insensitive Ca2+ channel from brain that most closely resembles the P-type channel described by Llinas and colleagues. These results contribute to rapidly growing knowledge about molecular determinants of Ca2+ channel diversity.
ISSN:0165-6147
DOI:10.1016/0165-6147(91)90595-j