Neuroscience Graduate Program, University of Ottawa, Ottawa, ON K1H 8M5, Canada; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON K1H 8M5, Canada.
Neuroscience Graduate Program, University of Ottawa, Ottawa, ON K1H 8M5, Canada; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON K1H 8M5, Canada; Canadian Partnership for Stroke Recovery, University of Ottawa, Ottawa, ON K1H 8M5, Canada; University of Ottawa Brain and Mind Research Institute's Centre for Neural Dynamics, Faculty of Medicine, University of Ottawa, Ottawa, ON K1H 8M5, Canada.
Cell Rep. 2017 Oct 31;21(5):1293-1303. doi: 10.1016/j.celrep.2017.10.025.
Hebbian and homeostatic forms of plasticity operate on different timescales to regulate synaptic strength. The degree of mechanistic overlap between these processes and their mutual influence are still incompletely understood. Here, we report that homeostatic synaptic strengthening induced by prolonged network inactivity compromised the ability of CA1 synapses to exhibit LTP. This effect could not be accounted for by an obvious deficit in the postsynaptic capacity for LTP expression, since neither the fraction of silent synapses nor the ability to induce LTP by two-photon glutamate uncaging were reduced by the homeostatic process. Rather, optical quantal analysis reveals that homeostatically strengthened synapses display a reduced capacity to maintain glutamate release fidelity during repetitive stimulation, ultimately impeding the induction, and thus expression, of LTP. By regulating the short-term dynamics of glutamate release, the homeostatic process thus influences key aspects of dynamic network function and exhibits features of metaplasticity.
Hebbian 和稳态形式的可塑性在不同的时间尺度上运作,以调节突触强度。这些过程之间的机制重叠程度及其相互影响仍不完全清楚。在这里,我们报告说,长时间网络不活动诱导的稳态突触强化削弱了 CA1 突触表现出 LTP 的能力。这种效应不能用 LTP 表达的突触后能力明显缺陷来解释,因为无论是沉默突触的分数还是通过双光子谷氨酸解笼来诱导 LTP 的能力都没有被稳态过程所减少。相反,光学量子分析表明,稳态强化的突触在重复刺激期间显示出维持谷氨酸释放保真度的能力降低,最终阻碍了 LTP 的诱导和表达。通过调节谷氨酸释放的短期动力学,稳态过程因此影响了动态网络功能的关键方面,并表现出了超可塑性的特征。