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一种用于培养在多电极阵列培养皿中的大鼠视交叉上核神经元放电率快速同步振荡的模型。

A model for the fast synchronous oscillations of firing rate in rat suprachiasmatic nucleus neurons cultured in a multielectrode array dish.

作者信息

Stepanyuk Andrey R, Belan Pavel V, Kononenko Nikolai I

机构信息

Bogomoletz Institute of Physiology, Kiev, Ukraine; State Key Laboratory of Molecular and Cellular Biology, Kiev, Ukraine.

出版信息

PLoS One. 2014 Sep 5;9(9):e106152. doi: 10.1371/journal.pone.0106152. eCollection 2014.

Abstract

When dispersed and cultured in a multielectrode dish (MED), suprachiasmatic nucleus (SCN) neurons express fast oscillations of firing rate (FOFR; fast relative to the circadian cycle), with burst duration ∼10 min, and interburst interval varying from 20 to 60 min in different cells but remaining nevertheless rather regular in individual cells. In many cases, separate neurons in distant parts of the 1 mm recording area of a MED exhibited correlated FOFR. Neither the mechanism of FOFR nor the mechanism of their synchronization among neurons is known. Based on recent data implicating vasoactive intestinal polypeptide (VIP) as a key intercellular synchronizing agent, we built a model in which VIP acts as both a feedback regulator to generate FOFR in individual neurons, and a diffusible synchronizing agent to produce coherent electrical output of a neuronal network. In our model, VIP binding to its (VPAC2) receptors acts through Gs G-proteins to activate adenylyl cyclase (AC), increase intracellular cAMP, and open cyclic-nucleotide-gated (CNG) cation channels, thus depolarizing the cell and generating neuronal firing to release VIP. In parallel, slowly developing homologous desensitization and internalization of VPAC2 receptors terminates elevation of cAMP and thereby provides an interpulse silent interval. Through mathematical modeling, we show that this VIP/VPAC2/AC/cAMP/CNG-channel mechanism is sufficient for generating reliable FOFR in single neurons. When our model for FOFR is combined with a published model of synchronization of circadian rhythms based on VIP/VPAC2 and Per gene regulation synchronization of circadian rhythms is significantly accelerated. These results suggest that (a) auto/paracrine regulation by VIP/VPAC2 and intracellular AC/cAMP/CNG-channels are sufficient to provide robust FOFR and synchrony among neurons in a heterogeneous network, and (b) this system may also participate in synchronization of circadian rhythms.

摘要

当视交叉上核(SCN)神经元在多电极培养皿(MED)中分散培养时,会表现出放电频率的快速振荡(FOFR;相对于昼夜节律周期而言速度很快),爆发持续时间约为10分钟,不同细胞的爆发间隔在20至60分钟之间变化,但在单个细胞中仍相当规律。在许多情况下,MED中1毫米记录区域远处的不同神经元表现出相关的FOFR。FOFR的产生机制及其在神经元之间的同步机制均尚不清楚。基于最近的数据表明血管活性肠肽(VIP)是关键的细胞间同步因子,我们构建了一个模型,其中VIP既作为反馈调节因子在单个神经元中产生FOFR,又作为可扩散的同步因子产生神经网络的相干电输出。在我们的模型中,VIP与其(VPAC2)受体结合通过Gs G蛋白作用激活腺苷酸环化酶(AC),增加细胞内cAMP,并打开环核苷酸门控(CNG)阳离子通道,从而使细胞去极化并产生神经元放电以释放VIP。同时,VPAC2受体缓慢发展的同源脱敏和内化终止了cAMP的升高,从而提供了脉冲间沉默间隔。通过数学建模,我们表明这种VIP/VPAC2/AC/cAMP/CNG通道机制足以在单个神经元中产生可靠的FOFR。当我们的FOFR模型与基于VIP/VPAC2和Per基因调节的昼夜节律同步的已发表模型相结合时,昼夜节律的同步显著加速。这些结果表明:(a)VIP/VPAC2的自分泌/旁分泌调节以及细胞内AC/cAMP/CNG通道足以在异质网络中神经元之间提供强大的FOFR和同步性;(b)该系统也可能参与昼夜节律的同步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50df/4156468/86e1b100a7cc/pone.0106152.g001.jpg

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