Biochemical Computation for Spine Structural Plasticity

被引:142
作者
Nishiyama, Jun [1 ]
Yasuda, Ryohei [1 ]
机构
[1] Max Planck Florida Inst Neurosci, Jupiter, FL 33458 USA
基金
日本学术振兴会;
关键词
LONG-TERM POTENTIATION; AMPA RECEPTOR TRAFFICKING; SINGLE DENDRITIC SPINES; HIPPOCAMPAL CA1 NEURONS; LOCAL PROTEIN-SYNTHESIS; SYNAPTIC PLASTICITY; NMDA-RECEPTOR; EXCITATORY SYNAPSES; ELECTRICAL COMPARTMENTALIZATION; FUNCTIONAL PLASTICITY;
D O I
10.1016/j.neuron.2015.05.043
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The structural plasticity of dendritic spines is considered to be essential for various forms of synaptic plasticity, learning, and memory. The process is mediated by a complex signaling network consisting of numerous species of molecules. Furthermore, the spatiotemporal dynamics of the biochemical signaling are regulated in a complicated manner because of geometrical restrictions from the unique morphology of the dendritic branches and spines. Recent advances in optical techniques have enabled the exploration of the spatiotemporal aspects of the signal regulations in spines and dendrites and have provided many insights into the principle of the biochemical computation that underlies spine structural plasticity.
引用
收藏
页码:63 / 75
页数:13
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