Mechanisms of Sleep-Dependent Consolidation of Cortical Plasticity

被引:170
作者
Aton, Sara J. [1 ]
Seibt, Julie [1 ]
Dumoulin, Michelle [1 ]
Jha, Sushil K. [1 ,2 ]
Steinmetz, Nicholas [1 ]
Coleman, Tammi [1 ]
Naidoo, Nirinjini [3 ]
Frank, Marcos G. [1 ]
机构
[1] Univ Penn, Dept Neurosci, Sch Med, Philadelphia, PA 19104 USA
[2] Jawaharlal Nehru Univ, Sch Life Sci, New Delhi 110067, India
[3] Univ Penn, Ctr Sleep & Resp Neurobiol, Sch Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
LONG-TERM POTENTIATION; HIPPOCAMPAL SYNAPTIC PLASTICITY; OCULAR DOMINANCE PLASTICITY; MEMORY CONSOLIDATION; VISUAL-CORTEX; DEVELOPMENTAL PLASTICITY; ORIENTATION SELECTIVITY; MONOCULAR DEPRIVATION; STRIATE CORTEX; EXPRESSION;
D O I
10.1016/j.neuron.2009.01.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sleep is thought to consolidate changes in synaptic strength, but the underlying mechanisms are unknown. We investigated the cellular events involved in this process during ocular dominance plasticity (ODP)-a canonical form of in vivo cortical plasticity triggered by monocular deprivation (MD) and consolidated by sleep via undetermined, activity-dependent mechanisms. We find that sleep consolidates ODP primarily by strengthening cortical responses to non-deprived eye stimulation. Consolidation is inhibited by reversible, intracortical antagonism of NMDA receptors (NMDARs) or cAMP-dependent protein kinase (PKA) during post-MD sleep. Consolidation is also associated with sleep-dependent increases in the activity of remodeling neurons and in the phosphorylation of proteins required for potentiation of glutamatergic synapses. These findings demonstrate that synaptic strengthening via NMDAR and PKA activity is a key step in sleep-dependent consolidation of ODP.
引用
收藏
页码:454 / 466
页数:13
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