Propagation of sharp wave-ripple activity in the mouse hippocampal CA3 subfield in vitro.

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Natalie Schieferstein, Ana Del Toro, Roberta Evangelista, Barbara Imbrosci, Aarti Swaminathan, Dietmar Schmitz, Nikolaus Maier, Richard Kempter
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引用次数: 0

Abstract

Sharp wave-ripple complexes (SPW-Rs) are spontaneous oscillatory events that characterize hippocampal activity during resting periods and slow-wave sleep. SPW-Rs are related to memory consolidation - the process during which newly acquired memories are transformed into long-lasting memory traces. To test the involvement of SPW-Rs in this process, it is crucial to understand how SPW-Rs originate and propagate throughout the hippocampus. SPW-Rs can originate in CA3, and they typically spread from CA3 to CA1, but little is known about their formation within CA3. To investigate the generation and propagation of SPW-Rs in CA3, we recorded from mouse hippocampal slices using multi-electrode arrays and patch-clamp electrodes. We characterized extracellular and intracellular correlates of SPW-Rs and quantified their propagation along the pyramidal cell layer of CA3. We found that a hippocampal slice can be described by a speed and a direction of propagation of SPW-Rs. The preferred propagation direction was from CA3c (the subfield closer to the dentate gyrus) toward CA3a (the subfield at the boundary to CA2). In patch-clamp recordings from CA3 pyramidal neurons, propagation was estimated separately for excitatory and inhibitory currents associated with SPW-Rs. We found that propagation speed and direction of excitatory and inhibitory currents were correlated. The magnitude of the speed of propagation of SPW-Rs within CA3 was consistent with the speed of propagation of action potentials in axons of CA3 principal cells. KEY POINTS: Hippocampal sharp waves are considered important for memory consolidation; therefore, it is of interest to understand the mechanisms of their generation and propagation. Here, we used two different approaches to study the propagation of sharp waves in mouse CA3 in vitro: multi-electrode arrays and multiple single-cell recordings. We find a preferred direction of propagation of sharp waves from CA3c toward CA3a - both in the local field potential and in sharp wave-associated excitatory and inhibitory synaptic activity. The speed of sharp wave propagation is consistent with the speed of action potential propagation along the axons of CA3 pyramidal neurons. These new insights into the dynamics of sharp waves in the CA3 network will inform future experiments and theoretical models of sharp-wave generation mechanisms.

体外小鼠海马 CA3 亚场锐波-瘫痪活动的传播。
锐波-跛行复合体(SPW-Rs)是一种自发振荡事件,是海马静息期和慢波睡眠期活动的特征。SPW-Rs与记忆巩固有关,即新获得的记忆转化为持久记忆痕迹的过程。要检验SPW-Rs是否参与了这一过程,了解SPW-Rs是如何在整个海马体中产生和传播的至关重要。SPW-Rs可以起源于CA3,而且通常会从CA3扩散到CA1,但人们对它们在CA3内的形成知之甚少。为了研究SPW-Rs在CA3中的产生和传播,我们使用多电极阵列和贴片钳电极对小鼠海马切片进行了记录。我们描述了 SPW-Rs 在细胞外和细胞内的相关性,并量化了它们沿着 CA3 锥体细胞层的传播。我们发现,海马切片可以用SPW-Rs的传播速度和方向来描述。SPW-Rs的首选传播方向是从CA3c(更靠近齿状回的亚区)向CA3a(与CA2交界的亚区)传播。在CA3锥体神经元的贴片钳记录中,分别估算了与SPW-Rs相关的兴奋性电流和抑制性电流的传播。我们发现,兴奋电流和抑制电流的传播速度和方向是相关的。SPW-Rs在CA3内的传播速度大小与CA3主细胞轴突中动作电位的传播速度一致。要点:海马尖波被认为对记忆巩固很重要,因此了解其产生和传播机制很有意义。在这里,我们使用了两种不同的方法来研究小鼠 CA3 体外尖波的传播:多电极阵列和多个单细胞记录。我们发现尖波从 CA3c 向 CA3a 传播的优先方向--在局部场电位和尖波相关的兴奋和抑制突触活动中都是如此。尖波的传播速度与沿着 CA3 锥体神经元轴突的动作电位传播速度一致。这些关于 CA3 网络中尖波动态的新见解将为未来的实验和尖波产生机制的理论模型提供参考。
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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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