AMPA receptor trafficking and learning

被引:81
|
作者
Keifer, J. [1 ]
Zheng, Z. [1 ]
机构
[1] Univ S Dakota, Nanosci Grp, Div Basic Biomed Sci, Sanford Sch Med, Vermillion, SD 57069 USA
关键词
Alzheimer's disease; classical conditioning; eyeblink; fear conditioning; spatial learning; LONG-TERM POTENTIATION; AMYLOID PRECURSOR PROTEIN; PREFRONTAL CORTEX NEURONS; NEUROTROPHIC FACTOR; ALZHEIMERS-DISEASE; SYNAPTIC PLASTICITY; GLUTAMATE-RECEPTOR; SPATIAL MEMORY; IMMUNOCYTOCHEMICAL LOCALIZATION; GLUR4-CONTAINING AMPARS;
D O I
10.1111/j.1460-9568.2010.07339.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the last few years it has become clear that AMPA-type glutamate neurotransmitter receptors are rapidly transported into and out of synapses to strengthen or weaken their function. The remarkable dynamics of AMPA receptor (AMPAR) synaptic localization provides a compelling mechanism for understanding the cellular basis of learning and memory, as well as disease states involving cognitive dysfunction. Here, we summarize the evidence for AMPAR trafficking as a mechanism underlying a variety of learned responses derived from both behavioral and cellular studies. Evidence is also reviewed supporting synaptic dysfunction related to impaired AMPAR trafficking as a mechanism underlying learning and memory deficits in Alzheimer's disease. We conclude that emerging data support the concept of multistage AMPAR trafficking during learning and that a broad approach to include examination of all of the AMPAR subunits will provide a more complete view of the mechanisms underlying multiple forms of learning.
引用
收藏
页码:269 / 277
页数:9
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