State Based Model of Long-Term Potentiation and Synaptic Tagging and Capture

被引:52
作者
Barrett, Adam B. [1 ]
Billings, Guy O. [1 ]
Morris, Richard G. M. [2 ]
van Rossum, Mark C. W. [1 ]
机构
[1] Univ Edinburgh, Inst Adapt & Neural Computat, Edinburgh, Midlothian, Scotland
[2] Univ Edinburgh, Ctr Cognit & Neural Syst, Edinburgh, Midlothian, Scotland
基金
英国工程与自然科学研究理事会;
关键词
PROTEIN-SYNTHESIS; HIPPOCAMPAL CA1; LATE MAINTENANCE; IN-VITRO; LATE-ASSOCIATIVITY; AMPA RECEPTORS; LTP; PLASTICITY; DEPRESSION; KINASE;
D O I
10.1371/journal.pcbi.1000259
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Recent data indicate that plasticity protocols have not only synapse-specific but also more widespread effects. In particular, in synaptic tagging and capture (STC), tagged synapses can capture plasticity-related proteins, synthesized in response to strong stimulation of other synapses. This leads to long-lasting modification of only weakly stimulated synapses. Here we present a biophysical model of synaptic plasticity in the hippocampus that incorporates several key results from experiments on STC. The model specifies a set of physical states in which a synapse can exist, together with transition rates that are affected by high-and low-frequency stimulation protocols. In contrast to most standard plasticity models, the model exhibits both early-and late-phase LTP/D, de-potentiation, and STC. As such, it provides a useful starting point for further theoretical work on the role of STC in learning and memory.
引用
收藏
页数:12
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