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Lengyel, M.

Publications and source records attributed to Lengyel, M..

2 recordsLinked to original sources

Global, multiplexed dendritic computations under in vivo-like conditions

Dendrites integrate inputs in highly non-linear ways, but it is unclear how these non-linearities contribute to the overall input-output transformation of single neurons. Here, we developed statistically principled methods using a hierarchical cascade of linear-nonlinear subunits (hLN) to model the dynamically evolving somatic response of neurons receiving complex spatio-temporal synaptic input patterns. We used the hLN to predict the membrane potential of a detailed biophysical model of a L2/3 pyramidal cell receiving in vivo-like synaptic input and reproducing in vivo dendritic recordings. We found that more than 90% of the somatic response could be captured by linear integration followed a single global non-linearity. Multiplexing inputs into parallel processing channels could improve prediction accuracy by as much as additional layers of local non-linearities. These results provide a data-driven characterisation of a key building block of cortical circuit computations: dendritic integration and the input-output transformation of single neurons during in vivo-like conditions.

neuroscience

Stabilized supralinear network dynamics account for stimulus-induced changes of noise variability in the cortex

Variability and correlations in cortical activity are ubiquitously modulated by stimuli. Correlated variability is quenched following stimulus onset across multiple cortical areas, suppressing low-frequency components of the LFP and of Vm-LFP coherence. Modulation of Fano factors and correlations in area MT is tuned for stimulus direction. What circuit mechanisms underly these behaviors? We show that a simple model circuit, the stochastic Stabilized Supralinear Network (SSN), robustly explains these results. Stimuli modulate variability by modifying two forms of effective connectivity between activity patterns that characterize excitatory-inhibitory (E/I) circuits. Increases in the strength with which activity patterns inhibit themselves reduce correlated variability, while increases in feedforward connections between patterns (transforming E/I imbalance into balanced fluctuations) increase variability. These results suggest an operating regime of cortical dynamics that involves fast fluctuations and fast responses to stimulus changes, unlike previous models of variability suppression through suppression of chaos or networks with multiple attractors.

neuroscience