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本文引用的文献

1
Consequences of the stoichiometry of Slo1 alpha and auxiliary beta subunits on functional properties of large-conductance Ca2+-activated K+ channels.Slo1α亚基与辅助β亚基的化学计量对大电导Ca2+激活K+通道功能特性的影响
J Neurosci. 2002 Mar 1;22(5):1550-61. doi: 10.1523/JNEUROSCI.22-05-01550.2002.
2
Modeling hair cell tuning by expression gradients of potassium channel beta subunits.通过钾通道β亚基的表达梯度对毛细胞调谐进行建模。
Biophys J. 2002 Jan;82(1 Pt 1):64-75. doi: 10.1016/S0006-3495(02)75374-5.
3
Tonotopic map of potassium currents in chick auditory hair cells using an intact basilar papilla.使用完整的基底乳头绘制雏鸡听觉毛细胞中钾电流的音频定位图。
Hear Res. 2001 Jun;156(1-2):81-94. doi: 10.1016/s0378-5955(01)00269-6.
4
Allosteric linkage between voltage and Ca(2+)-dependent activation of BK-type mslo1 K(+) channels.电压与BK型mslo1钾通道的钙依赖性激活之间的变构联系。
Biochemistry. 2000 Dec 19;39(50):15612-9. doi: 10.1021/bi001509+.
5
Role of the beta1 subunit in large-conductance Ca(2+)-activated K(+) channel gating energetics. Mechanisms of enhanced Ca(2+) sensitivity.β1亚基在大电导钙激活钾通道门控能量学中的作用。增强钙敏感性的机制。
J Gen Physiol. 2000 Sep;116(3):411-32. doi: 10.1085/jgp.116.3.411.
6
Voltage and Ca2+ activation of single large-conductance Ca2+-activated K+ channels described by a two-tiered allosteric gating mechanism.通过两层变构门控机制描述的单个大电导Ca2+激活K+通道的电压和Ca2+激活。
J Gen Physiol. 2000 Jul 1;116(1):75-99. doi: 10.1085/jgp.116.1.75.
7
beta subunits modulate alternatively spliced, large conductance, calcium-activated potassium channels of avian hair cells.β亚基调节鸟类毛细胞中可变剪接的、大电导的钙激活钾通道。
J Neurosci. 2000 Mar 1;20(5):1675-84. doi: 10.1523/JNEUROSCI.20-05-01675.2000.
8
The role of Ca2+-activated K+ channel spliced variants in the tonotopic organization of the turtle cochlea.钙离子激活钾通道剪接变体在龟类耳蜗音调组织中的作用。
J Physiol. 1999 Aug 1;518 ( Pt 3)(Pt 3):653-65. doi: 10.1111/j.1469-7793.1999.0653p.x.
9
The functional role of alternative splicing of Ca(2+)-activated K+ channels in auditory hair cells.Ca(2+)激活钾通道的可变剪接在听觉毛细胞中的功能作用。
Ann N Y Acad Sci. 1999 Apr 30;868:379-85. doi: 10.1111/j.1749-6632.1999.tb11299.x.
10
Mechanisms of hair cell tuning.毛细胞调谐的机制。
Annu Rev Physiol. 1999;61:809-34. doi: 10.1146/annurev.physiol.61.1.809.

鸡基底乳头毛细胞中大通量钙激活钾通道的变异

Variation in large-conductance, calcium-activated potassium channels from hair cells along the chicken basilar papilla.

作者信息

Duncan R K, Fuchs P A

机构信息

Department of Otolaryngology: Head and Neck Surgery, Johns Hopkins University, 521 Traylor Building, 720 Rutland Avenue, Baltimore, MD 21205, USA.

出版信息

J Physiol. 2003 Mar 1;547(Pt 2):357-71. doi: 10.1113/jphysiol.2002.029785. Epub 2003 Jan 17.

DOI:10.1113/jphysiol.2002.029785
PMID:12562934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2342658/
Abstract

The mechanism for electrical tuning in non-mammalian hair cells rests within the widely diverse kinetics of functionally distinct, large-conductance potassium channels (BK), thought to result from alternative splicing of the pore-forming alpha subunit and variable co-expression with an accessory beta subunit. Inside-out patches from hair cells along the chicken basilar papilla revealed 'tonotopic' gradations in calcium sensitivity and deactivation kinetics. The resonant frequency for the hair cell from which the patch was taken was estimated from deactivation rates, and this frequency reasonably matched that predicted from the originating cell's tonotopic location. The rates of deactivation for native BK channels were much faster than rates reported for cloned chicken BK channels including both alpha and beta subunits. This result was surprising since patches were pulled from hair cells in the apical half of the papilla where beta subunits are most highly expressed. Heterogeneity in the properties of native chicken BK channels implies a high degree of molecular variation and hinders our ability to identify those molecular constituents.

摘要

非哺乳动物毛细胞电调谐的机制在于功能各异的大电导钾通道(BK)具有广泛多样的动力学特性,这被认为是由孔形成α亚基的可变剪接以及与辅助β亚基的可变共表达所致。沿鸡基底乳头的毛细胞进行的内面向外膜片钳记录显示,钙敏感性和失活动力学存在“音频拓扑”梯度。根据失活速率估算了进行膜片钳记录的毛细胞的共振频率,该频率与根据起源细胞的音频拓扑位置预测的频率合理匹配。天然BK通道的失活速率比报道的包括α和β亚基的克隆鸡BK通道的失活速率快得多。这一结果令人惊讶,因为膜片是从乳头顶端一半的毛细胞中获取的,而此处β亚基表达最为丰富。天然鸡BK通道特性的异质性意味着分子变异程度很高,阻碍了我们识别这些分子成分的能力。