Thematic Minireview Series: Molecular Mechanisms of Synaptic Plasticity

被引:19
|
作者
Colbran, Roger J. [1 ,2 ]
机构
[1] Vanderbilt Univ, Sch Med, Vanderbilt Brain Inst, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Vanderbilt Kennedy Ctr, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
brain; glutamate receptor; neuron; signaling; synaptic plasticity; CAMKII;
D O I
10.1074/jbc.R115.696468
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human brain contains approximate to 86 billion neurons, which are precisely organized in specific brain regions and nuclei. High fidelity synaptic communication between subsets of neurons in specific circuits is required for most human behaviors, and is often disrupted in neuropsychiatric disorders. The presynaptic axon terminals of one neuron release neurotransmitters that activate receptors on multiple postsynaptic neuron targets to induce electrical and chemical responses. Typically, postsynaptic neurons integrate signals from multiple presynaptic neurons at thousands of synaptic inputs to control downstream communication to the next neuron in the circuit. Importantly, the strength (or efficiency) of signal transmission at each synapse can be modulated on time scales ranging up to the lifetime of the organism. This synaptic plasticity leads to changes in overall neuronal circuit activity, resulting in behavioral modifications. This series of minireviews will focus on recent advances in our understanding of the molecular and cellular mechanisms that control synaptic plasticity.
引用
收藏
页码:28594 / 28595
页数:2
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