Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9882230 | Archives of Biochemistry and Biophysics | 2005 | 9 Pages |
Abstract
Ca2+-dependent regulation of the ion current through the α1Cβ2aα2δ-1 (L-type) calcium channel transiently expressed in HEK 293 cells was investigated using whole cell patch clamp method. Ca2+ or Na+ ions were used as a charge carrier. Intracellular Ca2+ was either buffered by 10 mM EGTA or 200 μM Ca2+ was added into non-buffered intracellular solution. Free intracellular Ca2+ inactivated permanently about 80% of the L-type calcium current. The L-type calcium channel inactivated during a depolarizing pulse with two time constants, Ïfast and Ïslow. Free intracellular calcium accelerated both time constants. Effect on the Ïslow was more pronounced. About 80% of the channel inactivation during brief depolarizing pulse could be attributed to a Ca2+-dependent mechanism and 20% to a voltage-dependent mechanism. When Na+ ions were used as a charge carrier, the L-type current still inactivated with two time constants that were 10 times slower and were virtually voltage-independent. Ca2+ ions stabilized the inactivated state of the channel in a concentration-dependent manner.
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Authors
L'. Lacinová, F. Hofmann,