Suppr超能文献

BK 通道对小脑浦肯野神经元后电位和爆发性放电的调节作用。

BK Channel Regulation of Afterpotentials and Burst Firing in Cerebellar Purkinje Neurons.

机构信息

Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115.

Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115

出版信息

J Neurosci. 2021 Mar 31;41(13):2854-2869. doi: 10.1523/JNEUROSCI.0192-20.2021. Epub 2021 Feb 16.

Abstract

BK calcium-activated potassium channels have complex kinetics because they are activated by both voltage and cytoplasmic calcium. The timing of BK activation and deactivation during action potentials determines their functional role in regulating firing patterns but is difficult to predict a priori. We used action potential clamp to characterize the kinetics of voltage-dependent calcium current and BK current during action potentials in Purkinje neurons from mice of both sexes, using acutely dissociated neurons that enabled rapid voltage clamp at 37°C. With both depolarizing voltage steps and action potential waveforms, BK current was entirely dependent on calcium entry through voltage-dependent calcium channels. With voltage steps, BK current greatly outweighed the triggering calcium current, with only a brief, small net inward calcium current before Ca-activated BK current dominated the total Ca-dependent current. During action potential waveforms, although BK current activated with only a short (∼100 μs) delay after calcium current, the two currents were largely separated, with calcium current flowing during the falling phase of the action potential and most BK current flowing over several milliseconds after repolarization. Step depolarizations activated both an iberiotoxin-sensitive BK component with rapid activation and deactivation kinetics and a slower-gating iberiotoxin-resistant component. During action potential firing, however, almost all BK current came from the faster-gating iberiotoxin-sensitive channels, even during bursts of action potentials. Inhibiting BK current had little effect on action potential width or a fast afterhyperpolarization but converted a medium afterhyperpolarization to an afterdepolarization and could convert tonic firing of single action potentials to burst firing. BK calcium-activated potassium channels are widely expressed in central neurons. Altered function of BK channels is associated with epilepsy and other neuronal disorders, including cerebellar ataxia. The functional role of BK in regulating neuronal firing patterns is highly dependent on the context of other channels and varies widely among different types of neurons. Most commonly, BK channels are activated during action potentials and help produce a fast afterhyperpolarization. We find that in Purkinje neurons BK current flows primarily after the fast afterhyperpolarization and helps to prevent a later afterdepolarization from producing rapid burst firing, enabling typical regular tonic firing.

摘要

BK 钙激活钾通道具有复杂的动力学特性,因为它们既受电压又受细胞质钙的激活。在动作电位期间,BK 的激活和失活的时间决定了它们在调节放电模式中的功能作用,但很难事先预测。我们使用动作电位钳,通过急性分离神经元在 37°C 下进行快速电压钳,在来自雌雄小鼠的浦肯野神经元中,在动作电位期间,对电压依赖性钙电流和 BK 电流的动力学进行了特征描述。使用去极化电压步长和动作电位波形,BK 电流完全依赖于通过电压依赖性钙通道的钙内流。对于电压步长,BK 电流大大超过触发钙电流,在钙激活 BK 电流主导总钙依赖性电流之前,只有短暂的、小的净内向钙电流。在动作电位波形期间,尽管 BK 电流在钙电流之后仅延迟约 100 μs 激活,但两种电流基本分离,钙电流在动作电位的下降相流动,而大部分 BK 电流在复极化后数毫秒内流动。电压阶跃激活了具有快速激活和失活动力学的伊比替定敏感的 BK 成分和较慢门控的伊比替定抗性成分。然而,在动作电位放电期间,几乎所有的 BK 电流都来自快速门控的伊比替定敏感通道,即使在动作电位爆发期间也是如此。抑制 BK 电流对动作电位宽度或快速后超极化几乎没有影响,但将中后超极化转换为后去极化,并可将单动作电位的持续放电转换为爆发放电。BK 钙激活钾通道在中枢神经元中广泛表达。BK 通道功能的改变与癫痫和其他神经元疾病有关,包括小脑共济失调。BK 在调节神经元放电模式中的功能作用高度依赖于其他通道的背景,并且在不同类型的神经元之间差异很大。最常见的是,BK 通道在动作电位期间激活,并有助于产生快速后超极化。我们发现,在浦肯野神经元中,BK 电流主要在快速后超极化之后流动,并有助于防止迟发性后去极化产生快速爆发放电,从而实现典型的规则持续放电。

相似文献

1
BK Channel Regulation of Afterpotentials and Burst Firing in Cerebellar Purkinje Neurons.
J Neurosci. 2021 Mar 31;41(13):2854-2869. doi: 10.1523/JNEUROSCI.0192-20.2021. Epub 2021 Feb 16.
4
Iberiotoxin-sensitive and -insensitive BK currents in Purkinje neuron somata.
J Neurophysiol. 2013 May;109(10):2528-41. doi: 10.1152/jn.00127.2012. Epub 2013 Feb 27.
5
Ionic mechanisms of burst firing in dissociated Purkinje neurons.
J Neurosci. 2003 Oct 22;23(29):9650-63. doi: 10.1523/JNEUROSCI.23-29-09650.2003.
7
Dendritic control of spontaneous bursting in cerebellar Purkinje cells.
J Neurosci. 2004 Apr 7;24(14):3511-21. doi: 10.1523/JNEUROSCI.0290-04.2004.
8
Characterization of large conductance Ca2+-activated K+ channels in cerebellar Purkinje neurons.
Eur J Neurosci. 2002 Oct;16(7):1214-22. doi: 10.1046/j.1460-9568.2002.02171.x.

引用本文的文献

1
Unreliable homeostatic action potential broadening in cultured dissociated neurons.
bioRxiv. 2025 May 15:2025.05.09.653135. doi: 10.1101/2025.05.09.653135.
2
Neuropeptide-Dependent Spike Time Precision and Plasticity in Circadian Output Neurons.
Eur J Neurosci. 2025 Mar;61(5):e70037. doi: 10.1111/ejn.70037.
3
Ca-Activated Ion Channels Exert Opposite Effects in Different Signaling Compartments of Vomeronasal Sensory Neurons.
J Neurosci. 2025 Apr 16;45(16):e2134242025. doi: 10.1523/JNEUROSCI.2134-24.2025.
7
Neuropeptide-dependent spike time precision and plasticity in circadian output neurons.
bioRxiv. 2024 Dec 21:2024.10.06.616871. doi: 10.1101/2024.10.06.616871.
8
Involvement of BK Channels and Ryanodine Receptors in Salicylate-induced Tinnitus.
Mol Neurobiol. 2025 Apr;62(4):4115-4138. doi: 10.1007/s12035-024-04533-6. Epub 2024 Oct 14.

本文引用的文献

1
LINGO1 is a regulatory subunit of large conductance, Ca-activated potassium channels.
Proc Natl Acad Sci U S A. 2020 Jan 28;117(4):2194-2200. doi: 10.1073/pnas.1916715117. Epub 2020 Jan 13.
2
The functionally relevant site for paxilline inhibition of BK channels.
Proc Natl Acad Sci U S A. 2020 Jan 14;117(2):1021-1026. doi: 10.1073/pnas.1912623117. Epub 2019 Dec 26.
4
-linked channelopathy.
J Gen Physiol. 2019 Oct 7;151(10):1173-1189. doi: 10.1085/jgp.201912457. Epub 2019 Aug 19.
6
Regulation of BK Channels by Beta and Gamma Subunits.
Annu Rev Physiol. 2019 Feb 10;81:113-137. doi: 10.1146/annurev-physiol-022516-034038.
8
Physiological Roles and Therapeutic Potential of Ca Activated Potassium Channels in the Nervous System.
Front Mol Neurosci. 2018 Jul 30;11:258. doi: 10.3389/fnmol.2018.00258. eCollection 2018.
9
Dendritic potassium channel dysfunction may contribute to dendrite degeneration in spinocerebellar ataxia type 1.
PLoS One. 2018 May 30;13(5):e0198040. doi: 10.1371/journal.pone.0198040. eCollection 2018.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验