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本文引用的文献

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Metabolic differences in hippocampal 'Rett' neurons revealed by ATP imaging.通过 ATP 成像揭示海马体“雷特”神经元的代谢差异。
Mol Cell Neurosci. 2014 Mar;59:47-56. doi: 10.1016/j.mcn.2013.12.008. Epub 2014 Jan 3.
2
Nanoscale-targeted patch-clamp recordings of functional presynaptic ion channels.纳米级靶向膜片钳记录功能性突触前离子通道。
Neuron. 2013 Sep 18;79(6):1067-77. doi: 10.1016/j.neuron.2013.07.012.
3
Tuning local calcium availability: cell-type-specific immobile calcium buffer capacity in hippocampal neurons.调节局部钙可用性:海马神经元中细胞类型特异性不可移动钙缓冲能力。
J Neurosci. 2013 Sep 4;33(36):14431-45. doi: 10.1523/JNEUROSCI.4118-12.2013.
4
Modeling interactions between voltage-gated Ca (2+) channels and KCa1.1 channels.模拟电压门控钙(2+)通道与钙激活钾通道1.1(KCa1.1)之间的相互作用。
Channels (Austin). 2013 Nov-Dec;7(6):524-9. doi: 10.4161/chan.25867. Epub 2013 Jul 31.
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DNA transfection: calcium phosphate method.DNA转染:磷酸钙法。
Methods Mol Biol. 2013;1018:107-10. doi: 10.1007/978-1-62703-444-9_10.
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Low voltage activation of KCa1.1 current by Cav3-KCa1.1 complexes.Cav3-KCa1.1 复合物对 KCa1.1 电流的低电压激活。
PLoS One. 2013 Apr 23;8(4):e61844. doi: 10.1371/journal.pone.0061844. Print 2013.
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Iberiotoxin-sensitive and -insensitive BK currents in Purkinje neuron somata.蒲肯野神经元胞体中伊贝毒素敏感和不敏感 BK 电流。
J Neurophysiol. 2013 May;109(10):2528-41. doi: 10.1152/jn.00127.2012. Epub 2013 Feb 27.
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Quantitative localization of Cav2.1 (P/Q-type) voltage-dependent calcium channels in Purkinje cells: somatodendritic gradient and distinct somatic coclustering with calcium-activated potassium channels.定量定位浦肯野细胞中的 Cav2.1(P/Q 型)电压依赖性钙通道:树突-胞体梯度和与钙激活钾通道的明显共簇。
J Neurosci. 2013 Feb 20;33(8):3668-78. doi: 10.1523/JNEUROSCI.2921-12.2013.
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Nanodomain coupling at an excitatory cortical synapse.兴奋型皮质突触的纳米域偶联。
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Stochastic resonance in Hodgkin-Huxley neuron induced by unreliable synaptic transmission.由不可靠突触传递引起的 Hodgkin-Huxley 神经元中的随机共振。
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在单复合体水平上模拟钙通道/大电导钙激活钾通道复合体

Modeling a Ca(2+) channel/BKCa channel complex at the single-complex level.

作者信息

Cox Daniel H

机构信息

Department of Neuroscience, Tufts University School of Medicine, Boston, Massachusetts.

出版信息

Biophys J. 2014 Dec 16;107(12):2797-2814. doi: 10.1016/j.bpj.2014.10.069.

DOI:10.1016/j.bpj.2014.10.069
PMID:25517147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4269775/
Abstract

BKCa-channel activity often affects the firing properties of neurons, the shapes of neuronal action potentials (APs), and in some cases the extent of neurotransmitter release. It has become clear that BKCa channels often form complexes with voltage-gated Ca(2+) channels (CaV channels) such that when a CaV channel is activated, the ensuing influx of Ca(2+) activates its closely associated BKCa channel. Thus, in modeling the electrical properties of neurons, it would be useful to have quantitative models of CaV/BKCa complexes. Furthermore, in a population of CaV/BKCa complexes, all BKCa channels are not exposed to the same Ca(2+) concentration at the same time. Thus, stochastic rather than deterministic models are required. To date, however, no such models have been described. Here, however, I present a stochastic model of a CaV2.1/BKCa(α-only) complex, as might be found in a central nerve terminal. The CaV2.1/BKCa model is based on kinetic modeling of its two component channels at physiological temperature. Surprisingly, The CaV2.1/BKCa model predicts that although the CaV channel will open nearly every time during a typical cortical AP, its associated BKCa channel is expected to open in only 30% of trials, and this percentage is very sensitive to the duration of the AP, the distance between the two channels in the complex, and the presence of fast internal Ca(2+) buffers. Also, the model predicts that the kinetics of the BKCa currents of a population of CaV2.1/BKCa complexes will not be limited by the kinetics of the CaV2.1 channel, and during a train of APs, the current response of the complex is expected to faithfully follow even very rapid trains. Aside from providing insight into how these complexes are likely to behave in vivo, the models presented here could also be of use more generally as components of higher-level models of neural function.

摘要

大电导钙激活钾通道(BKCa通道)的活性常常影响神经元的放电特性、神经元动作电位(AP)的形状,在某些情况下还会影响神经递质释放的程度。目前已经明确,BKCa通道常常与电压门控钙通道(CaV通道)形成复合物,这样当一个CaV通道被激活时,随之而来的钙离子内流会激活与其紧密相连的BKCa通道。因此,在对神经元的电特性进行建模时,拥有CaV/BKCa复合物的定量模型将会很有用。此外,在一群CaV/BKCa复合物中,并非所有的BKCa通道都会同时暴露于相同的钙离子浓度下。因此,需要随机模型而非确定性模型。然而,迄今为止,尚未有此类模型被描述。不过,在此我提出了一种CaV2.1/BKCa(仅α亚基)复合物的随机模型,这种复合物可能存在于中枢神经末梢。CaV2.1/BKCa模型是基于其两个组成通道在生理温度下的动力学建模。令人惊讶的是,CaV2.1/BKCa模型预测,尽管在典型的皮层动作电位期间CaV通道几乎每次都会打开,但其相关的BKCa通道预计仅在30%的试验中打开,并且这个百分比对动作电位的持续时间、复合物中两个通道之间的距离以及快速胞内钙缓冲剂的存在非常敏感。此外,该模型预测,一群CaV2.1/BKCa复合物的BKCa电流动力学不会受到CaV2.1通道动力学的限制,并且在一串动作电位期间,复合物的电流响应预计会忠实地跟随甚至非常快速的一串动作电位。除了有助于深入了解这些复合物在体内可能的行为方式外,这里提出的模型作为神经功能高级模型的组成部分,在更广泛的层面上也可能会有用。