Abstract

The interaction between synaptic and intrinsic dynamics can efficiently shape neuronal input-output relationships in response to temporally structured spike trains. We use a neuron model with subthreshold oscillations receiving inputs through a synapse with short-term depression and facilitation to show that the combination of intrinsic subthreshold and synaptic dynamics leads to channel-specific nontrivial responses and recognition of specific temporal structures. We employ the Generalized Integrate-and-Fire (GIF) model, which can be subjected to analytical characterization. We map the temporal structure of spike input trains to the type of spike response, and show how the emergence of nontrivial input-output preferences is modulated by intrinsic and synaptic parameters in a synergistic manner. We demonstrate that these temporal input discrimination properties are robust to noise and to variations in synaptic strength, suggesting that they likely contribute to neuronal computation in biological circuits. Furthermore, we also illustrate the presence of these input-output relationships in conductance-based models.\n\nAuthor summaryNeuronal subthreshold oscillations underlie key aspects of information processing in single neuron and network dynamics. Dynamic synapses provide a channel-specific temporal modulation of input information. We combine a neuron model that displays subthreshold oscillations and a dynamic synapse to analytically assess their interplay in processing trains of spike-mediated synaptic currents. Our results show that the co-action of intrinsic and synaptic dynamics builds nontrivial input-output relationships, which are resistant to noise and to changes in synaptic strength. The discrimination of a precise temporal structure of the input signal is shaped as a function of the joint interaction of intrinsic oscillations and synaptic dynamics. This interaction can result in channel-specific recognition of precise temporal patterns, hence greatly expanding the flexibility and complexity in information processing achievable by individual neurons with respect to temporal discrimination mechanisms based on intrinsic neuronal dynamics alone.