Selective activation of Ca2+-activated K+ channels by co-localized Ca2+ channels in hippocampal neurons

被引:464
作者
Marrion, NV
Tavalin, SJ
机构
[1] Oregon Hlth Sci Univ, Vollum Inst, Portland, OR 97201 USA
[2] Univ Bristol, Sch Med Sci, Dept Pharmacol, Bristol BS8 1TD, Avon, England
关键词
D O I
10.1038/27674
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Calcium entry through voltage-gated calcium channels can activate either large- (BK) or small- (SK) conductance calcium-activated potassium channels. In hippocampal neurons, activation of BK channels underlies the falling phase of an action potential and generation of the fast afterhyperpolarization (AHP)(1,2). In contrast, SK channel activation underlies generation of the slow AHP after a burst of action potentials(3). The source of calcium for BK channel activation is unknown, but the slow AHP is blocked by dihydropyridine antagonists(4,5), indicating that L-type calcium channels provide the calcium for activation of SK channels. It is not understood how this specialized coupling between calcium and potassium channels is achieved, Here we study channel activity in cell-attached patches from hippocampal neurons and report a unique specificity of coupling. L-type channels activate SK channels only, without activating BK channels present in the same patch. The delay between the opening of L-type channels and SK channels indicates that these channels are 50-150 nm apart. In contrast, N-type calcium channels activate BK channels only, with opening of the two channel types being nearly coincident. This temporal association indicates that N and BK channels are very close. Finally, P/Q-type calcium channels do not couple to either SK or BK channels. These data indicate an absolute segregation of coupling between channels, and illustrate the functional importance of submembrane calcium microdomains.
引用
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页码:900 / 905
页数:6
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