Samarth Pranit, Ball John M, Unal Gunes, Paré Denis, Nair Satish S
Division of Biological Sciences and Department of Electrical and Computer Engineering, University of Missouri, Columbia, MO, 65211, USA.
Center for Molecular and Behavioral Neuroscience, Rutgers University-Newark, Newark, NJ, 07102, USA.
Brain Struct Funct. 2017 Jan;222(1):183-200. doi: 10.1007/s00429-016-1210-4. Epub 2016 Mar 12.
The perirhinal cortex supports recognition and associative memory. Prior unit recording studies revealed that recognition memory involves a reduced responsiveness of perirhinal cells to familiar stimuli whereas associative memory formation is linked to increasing perirhinal responses to paired stimuli. Both effects are thought to depend on perirhinal plasticity but it is unclear how the same network could support these opposite forms of plasticity. However, a recent study showed that when neocortical inputs are repeatedly activated, depression or potentiation could develop, depending on the extent to which the stimulated neocortical activity recruited intrinsic longitudinal connections. We developed a biophysically realistic perirhinal model that reproduced these phenomena and used it to investigate perirhinal mechanisms of associative memory. These analyzes revealed that associative plasticity is critically dependent on a specific subset of neurons, termed conjunctive cells (CCs). When the model network was trained with spatially distributed but coincident neocortical inputs, CCs acquired excitatory responses to the paired inputs and conveyed them to distributed perirhinal sites via longitudinal projections. CC ablation during recall abolished expression of the associative memory. However, CC ablation during training did not prevent memory formation because new CCs emerged, revealing that competitive synaptic interactions governs the formation of CC assemblies.
嗅周皮质支持识别和联想记忆。先前的单位记录研究表明,识别记忆涉及嗅周细胞对熟悉刺激的反应性降低,而联想记忆的形成则与嗅周细胞对配对刺激的反应增加有关。这两种效应都被认为依赖于嗅周可塑性,但尚不清楚同一网络如何支持这些相反形式的可塑性。然而,最近的一项研究表明,当新皮质输入被反复激活时,根据受刺激的新皮质活动募集内在纵向连接的程度,可能会出现抑制或增强。我们开发了一个生物物理逼真的嗅周模型,该模型再现了这些现象,并用于研究联想记忆的嗅周机制。这些分析表明,联想可塑性关键取决于一个特定的神经元子集,称为联合细胞(CCs)。当模型网络用空间分布但同时出现的新皮质输入进行训练时,CCs获得了对配对输入的兴奋性反应,并通过纵向投射将它们传递到分布在各处的嗅周位点。回忆期间消融CCs消除了联想记忆的表达。然而,训练期间消融CCs并不能阻止记忆形成,因为新的CCs出现了,这表明竞争性突触相互作用控制着CCs集合的形成。