Nonlinear dendritic integration supports Up-Down states in single neurons

Abstract

Changes in the activity profile of cortical neurons are due to effects at the scale of local and long-range networks. Accordingly, abrupt transitions in the state of cortical neurons--a phenomenon known as Up-Down states--have been attributed to variation in the activity of afferent neurons. However, cellular physiology and morphology may also play a role in causing Up-Down states. This study examines the impact of dendritic nonlinearities, particularly those mediated by voltage-dependent NMDA receptors, on the response of cortical neurons to balanced excitatory/inhibitory synaptic inputs. Using a neuron model with two segregated dendritic compartments, we compared cells with and without dendritic nonlinearities. NMDA receptors boosted somatic firing in the balanced condition and increased the correlation between membrane potentials across the compartments of the neuron model. Dendritic nonlinearities elicited strong bimodality in the distribution of the somatic potential when the cell was driven with cortical-like input. Moreover, dendritic nonlinearities could detect small input fluctuations and lead to Up-Down states whose statistics and dynamics closely resemble electrophysiological data. Up-Down states also occurred in recurrent networks with oscillatory firing activity, as in anaesthetized animal models, when dendritic NMDA receptors were partially disabled. These findings suggest that there is a dissociation between cellular and network-level features that could both contribute to the emergence of Up-Down states. Our study highlights the complex interplay between dendritic integration and activity-driven dynamics in the origin of cortical bistability. Significance statementIn several physiological states, such as sleep or quiet wakefulness, the membrane of cortical cells shows characteristic bistability. Cells are either fully depolarized and ready to spike, or in a silent, hyperpolarized state. This dynamics, known as Up-Down states, has often been attributed to changes in network activity. However, whether cell-specific properties, such as dendritic nonlinearities, play a role in neuronal bistability remains unclear. This study uses a dendritic model of a pyramidal cell and shows that the presence of NMDA receptors drives the Up-Down states in response to small fluctuations in network activity. Thus, single cells can enter the Up-Down state dynamics independently of the ongoing network activity.