Irie Tomohiko, Trussell Laurence O
Oregon Hearing Research Center, Oregon Health & Science University, Portland, OR 97239, USA; Division of Pharmacology, National Institute of Health Sciences, Kanagawa 210-9501, Japan.
Oregon Hearing Research Center, Oregon Health & Science University, Portland, OR 97239, USA; Vollum Institute, Oregon Health & Science University, Portland, OR 97239, USA.
Neuron. 2017 Nov 15;96(4):856-870.e4. doi: 10.1016/j.neuron.2017.10.014.
Action potentials clustered into high-frequency bursts play distinct roles in neural computations. However, little is known about ionic currents that control the duration and probability of these bursts. We found that, in cartwheel inhibitory interneurons of the dorsal cochlear nucleus, the likelihood of bursts and the interval between their spikelets were controlled by Ca acting across two nanodomains, one between plasma membrane P/Q Ca channels and endoplasmic reticulum (ER) ryanodine receptors and another between ryanodine receptors and large-conductance, voltage- and Ca-activated K (BK) channels. Each spike triggered Ca-induced Ca release (CICR) from the ER immediately beneath somatic, but not axonal or dendritic, plasma membrane. Moreover, immunolabeling demonstrated close apposition of ryanodine receptors and BK channels. Double-nanodomain coupling between somatic plasma membrane and hypolemmal ER cisterns provides a unique mechanism for rapid control of action potentials on the millisecond timescale.
聚集为高频爆发的动作电位在神经计算中发挥着独特作用。然而,对于控制这些爆发的持续时间和概率的离子电流,我们却知之甚少。我们发现,在背侧耳蜗核的车轮状抑制性中间神经元中,爆发的可能性及其小尖峰之间的间隔是由跨两个纳米域作用的钙离子控制的,一个纳米域位于质膜P/Q型钙离子通道与内质网(ER)兰尼碱受体之间,另一个纳米域位于兰尼碱受体与大电导、电压和钙离子激活的钾(BK)通道之间。每个动作电位都会立即触发内质网在胞体(而非轴突或树突)质膜正下方的钙诱导钙释放(CICR)。此外,免疫标记显示兰尼碱受体与BK通道紧密相邻。胞体质膜与膜下内质网池之间的双纳米域耦合为在毫秒时间尺度上快速控制动作电位提供了一种独特机制。