Neuronal activity-dependent synaptic plasticity, a basis for learning and memory, is tightly correlated with the pattern of increase in intracellular Ca2+ concentration ([Ca2+]i). Here, using combined application of electrophysiological experiments and systems biological simulation, we show that such a correlation dynamically changes depending on the context of [Ca2+]i increase. In a cerebellar Purkinje cell, long-term potentiation of inhibitory GABAA receptor responsiveness (called rebound potentiation; RP) was induced by [Ca2+]i increase in a temporally integrative manner through sustained activation of Ca2+/calmodulin-dependent protein kinase II (CaMKII). However, the RP establishment was canceled by coupling of two patterns of RP-inducing [Ca2+]i increase depending on the temporal sequence. Negative feedback signaling by phospho-Thr305/306 CaMKII detected the [Ca2+]i context, and assisted the feedforward inhibition of CaMKII through PDE1, resulting in the RP impairment. The [Ca2+]i context-dependent dynamic regulation of synaptic plasticity might contribute to the temporal refinement of information flow in neuronal networks.
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