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Molecular regulation of synaptogenesis during associative learning and memory

机译:联想学习和记忆过程中突触发生的分子调控。

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摘要

Synaptogenesis plays a central role in associative learning and memory. The biochemical pathways that underlie synaptogenesis are complex and incompletely understood. Nevertheless, research has so far identified three conceptually distinct routes to synaptogenesis: cell-cell contact mediated by adhesion proteins, cell-cell biochemical signaling from astrocytes and other cells, and neuronal signaling through classical ion channels and cell surface receptors. The cell adhesion pathways provide the physical substrate to the new synaptic connection, while cell-cell signaling may provide a global or regional signal, and the activity-dependent pathways provide the neuronal specificity that is required for the new synapses to produce functional neuronal networks capable of storing associative memories. These three aspects of synaptogenesis require activation of a variety of interacting biochemical pathways that converge on the actin cytoskeleton and strengthen the synapse in an information-dependent manner.
机译:突触发生在联想学习和记忆中起着核心作用。突触形成基础的生化途径是复杂的,尚未完全理解。尽管如此,到目前为止,研究已经确定了三种在突触发生上在概念上截然不同的途径:由粘附蛋白介导的细胞间接触,星形胶质细胞和其他细胞的细胞间生化信号传导以及通过经典离子通道和细胞表面受体的神经元信号传导。细胞粘附途径为新的突触连接提供了物理底物,而细胞间信号传导可能提供了全局或区域信号,而活性依赖性途径提供了新突触产生功能性神经元网络所需的神经元特异性。存储关联记忆。突触形成的这三个方面需要激活多种相互作用的生化途径,这些途径会聚集在肌动蛋白的细胞骨架上并以信息依赖的方式增强突触。

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