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van Vreeswijk, C.

Publications and source records attributed to van Vreeswijk, C..

5 recordsLinked to original sources

Emergence of Balanced Cortical Activity via Calcium-Regulated Synaptic Homeostasis

Cortical circuits must stabilize activity while retaining the variability and flexibility essential for computation. This raises a fundamental question: how can excitatory (E) and inhibitory (I) synapses co-adapt through homeostatic plasticity without disrupting network function or relying on fine-tuned parameters? We propose a solution grounded in the multidimensional nature of intracellular calcium signaling, which independently regulates protein synthesis at E and I synapses. By analytically characterizing calcium dynamics driven by spike-train statistics, we show that calciums mean encodes firing rate while its variance reflects spike-time irregularity--two complementary features critical for stable yet flexible spiking. Leveraging this dual signal, we construct a closed-loop model in which inhibitory synapses are regulated by calciums mean and excitatory synapses by its variance through independent pathways. This mechanism preserves irregular spiking and stabilizes firing rates across diverse inputs. Strikingly, it also yields the empirically observed weakening of synaptic strengths with the number of inputs K as [Formula], leading to the spontaneous emergence of balanced excitatory-inhibitory dynamics. These results uncover a calcium-driven regulatory principle linking intracellular signaling to the origin of balanced activity in cortical networks.

neuroscience↗

Noise-induced properties of active dendrites

Dendrites play an essential role in the integration of highly fluctuating input into neurons across all nervous systems. Nevertheless, they are often studied under the conditions where inputs to dendrites are sparse. Up to date, the dynamic properties of active dendrites facing in-vivo-like fluctuating input remains elusive. In this paper, we uncover fundamentally new dynamics in a canonical model of a dendritic compartment with active calcium channels, receiving in-vivo-like fluctuating input. We show in-vivo-like noise induces non-monotonic or bistable dynamics in the input-output relation of a dendritic compartment, both of which are absent in a noiseless condition. Our analysis shows that the timescales of the activation gating variable of the dendritic calcium dynamics determine noise-induced spontaneous order in the system. Noise can induce non-monotonicity or bistability with fast or slow calcium activation respectively. We characterize these noise-induced phenomena and their influence on the input-output relation. Furthermore, we show that timescales of the emerging stochastic bistable dynamics go far beyond a deterministic system due to stochastic switching between the solutions. Our results reveal that noise contributes to sustained dendritic nonlinearities, and it could be considered a principal component of the dendritic input integration strategies.

neuroscience↗

Mechanisms underlying the response of mouse cortical networks to optogenetic manipulation

GABAergic interneurons can be subdivided into three subclasses: parvalbumin positive (PV), somatostatin positive (SOM) and serotonin positive neurons. With principal cells (PCs) they form complex networks. We examine PCs and PV responses in mouse anterior lateral motor cortex (ALM) and barrel cortex (S1) upon PV photostimulation in vivo. In layer 5, the PV response is paradoxical: photoexcitation reduces their activity. This is not the case in ALM layer 2/3. We combine analytical calculations and numerical simulations to investigate how these results constrain the architecture. Two-population models cannot account for the results. Networks with three inhibitory populations and V1-like architecture account for the data in ALM layer 2/3. Our data in layer 5 can be accounted for if SOM neurons receive inputs only from PCs and PV neurons. In both four-population models, the paradoxical effect implies not too strong recurrent excitation. It is not evidence for stabilization by inhibition.

neuroscience↗

Emergent orientation selectivity from random networks in mouse visual cortex

We study the connectivity principles underlying the emergence of orientation selectivity in primary visual cortex (V1) of mammals lacking an orientation map. We present a computational model in which random connectivity gives rise to orientation selectivity that matches experimental observations. It predicts that mouse V1 neurons should exhibit intricate receptive fields in the two-dimensional frequency domain, causing shift in orientation preferences with spatial frequency. We find evidence for these features in mouse V1 using calcium imaging and intracellular whole cell recordings.

neuroscience↗

How strong are correlations in strongly recurrent neuronal networks?

Cross-correlations in the activity in neural networks are commonly used to characterize their dynamical states and their anatomical and functional organizations. Yet, how these latter network features affect the spatiotemporal structure of the correlations in recurrent networks is not fully understood. Here, we develop a general theory for the emergence of correlated neuronal activity from the dynamics in strongly recurrent networks consisting of several populations of binary neurons. We apply this theory to the case in which the connectivity depends on the anatomical or functional distance between the neurons. We establish the architectural conditions under which the system settles into a dynamical state where correlations are strong, highly robust and spatially modulated. We show that such strong correlations arise if the network exhibits an effective feedforward structure. We establish how this feedforward structure determines the way correlations scale with the network size and the degree of the connectivity. In networks lacking an effective feedforward structure correlations are extremely small and only weakly depend on the number of connections per neuron. Our work shows how strong correlations can be consistent with highly irregular activity in recurrent networks, two key features of neuronal dynamics in the central nervous system.

neuroscience↗