Burgess Neil, Barry Caswell, O'Keefe John
Institute of Cognitive Neuroscience, University College London, 17 Queen Square, London, United Kingdom.
Hippocampus. 2007;17(9):801-12. doi: 10.1002/hipo.20327.
We expand upon our proposal that the oscillatory interference mechanism proposed for the phase precession effect in place cells underlies the grid-like firing pattern of dorsomedial entorhinal grid cells (O'Keefe and Burgess (2005) Hippocampus 15:853-866). The original one-dimensional interference model is generalized to an appropriate two-dimensional mechanism. Specifically, dendritic subunits of layer II medial entorhinal stellate cells provide multiple linear interference patterns along different directions, with their product determining the firing of the cell. Connection of appropriate speed- and direction-dependent inputs onto dendritic subunits could result from an unsupervised learning rule which maximizes postsynaptic firing (e.g. competitive learning). These inputs cause the intrinsic oscillation of subunit membrane potential to increase above theta frequency by an amount proportional to the animal's speed of running in the "preferred" direction. The phase difference between this oscillation and a somatic input at theta-frequency essentially integrates velocity so that the interference of the two oscillations reflects distance traveled in the preferred direction. The overall grid pattern is maintained in environmental location by phase reset of the grid cell by place cells receiving sensory input from the environment, and environmental boundaries in particular. We also outline possible variations on the basic model, including the generation of grid-like firing via the interaction of multiple cells rather than via multiple dendritic subunits. Predictions of the interference model are given for the frequency composition of EEG power spectra and temporal autocorrelograms of grid cell firing as functions of the speed and direction of running and the novelty of the environment.
我们进一步阐述了我们的观点,即针对位置细胞中相位进动效应所提出的振荡干扰机制,是背内侧内嗅皮层网格细胞网格状放电模式的基础(O'Keefe和Burgess(2005年),《海马体》15:853 - 866)。原始的一维干扰模型被推广为一种合适的二维机制。具体而言,内侧内嗅皮层II层星状细胞的树突亚基沿不同方向提供多个线性干扰模式,它们的乘积决定细胞的放电。将适当的速度和方向依赖输入连接到树突亚基上,可能源于一种无监督学习规则,该规则使突触后放电最大化(例如竞争学习)。这些输入使亚基膜电位的固有振荡增加到高于θ频率,增加的幅度与动物在“偏好”方向上的奔跑速度成正比。这种振荡与θ频率的体细胞输入之间的相位差本质上整合了速度,从而使两种振荡的干扰反映了在偏好方向上行进的距离。通过接收来自环境尤其是环境边界的感觉输入的位置细胞对网格细胞进行相位重置,整体网格模式在环境位置中得以维持。我们还概述了基本模型可能的变体,包括通过多个细胞而非多个树突亚基的相互作用产生网格状放电。针对脑电图功率谱的频率组成以及网格细胞放电的时间自相关图,给出了干扰模型的预测,这些预测是奔跑速度和方向以及环境新奇性的函数。