Molecular regulation of synaptogenesis during associative learning and memory

被引:21
作者
Nelson, Thomas J. [1 ]
Alkon, Daniel L. [1 ]
机构
[1] Blanchette Rockefeller Neurosci Inst, Morgantown, WV 26505 USA
关键词
Learning; Memory; Synaptogenesis; Protein kinase C; Synapse; BDNF; LONG-TERM POTENTIATION; PROTEIN-KINASE-C; EXCITATORY SYNAPSE FORMATION; ASTROCYTE-SECRETED PROTEINS; DENDRITIC SPINE MORPHOLOGY; ADULT VISUAL-CORTEX; BDNF MESSENGER-RNA; ALZHEIMERS-DISEASE; IN-VIVO; APOLIPOPROTEIN-E;
D O I
10.1016/j.brainres.2014.11.054
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
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. This article is part of a Special Issue titled SI: Brain and Memory. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 251
页数:13
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