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Synaptic-type-specific clustering optimizes the computational capabilities of balanced recurrent networks

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Citation

Giannakakis, E., Levina, A., Buendia, V., & Khajehabdollahi, S. (2023). Synaptic-type-specific clustering optimizes the computational capabilities of balanced recurrent networks. Poster presented at Computational and Systems Neuroscience Meeting (COSYNE 2023), Montreal, Quebec, Canada.


Cite as: https://hdl.handle.net/21.11116/0000-000C-9626-0
Abstract
The specific topology of biological neural networks is believed to be one of the most important ingredients of the nervous system’s computational capabilities. Furthermore, multiple experimental studies have demonstrated that neural connectivity is highly inhomogeneous, following different patterns between different regions and neuron types. In particular, the presence of clusters of highly interconnected neurons is one of the most well-established connectivity patterns across multiple brain areas. Still, the functional implications of such brain connectivity fea- tures, especially for the performance of specific tasks remain largely unknown. Here, we use a reservoir computing model to link diverse, synaptic type-specific levels of clustering in balanced recurrent networks with the ability to process multiple uncorrelated complex inputs simultaneously. We construct a balanced recurrent network of rate neurons, which we use as a reservoir that simultaneously predicts the trajectory of two chaotic attractors. Predicting the dynamics of a single chaotic system is a com- monly used task. For the more challenging simultaneous prediction, we split the network into two clusters, each responsible for processing one attractor. We investigate whether synaptic connections between the two clusters can benefit the reservoir’s performance. In particular, we hypothesize that different probabilities of connection within and between clusters for different types of synapses could improve the network’s ability to process complex dynamics. Thus, we use approximate Bayesian computation to estimate the distribution of synapse type-specific clustering levels that lead to optimal network performance. We find that localized excitation, combined with more spread-out inhibition (a pattern observed in cortical networks), boosts the network’s performance. Our findings suggest that contrary to common intuition, overlapping connectivity between sub-networks perform- ing different tasks can lead to beneficial dynamics that enhance task performance. Thus, commonly observed connectivity patterns in the brain could have a functional role in the parallel processing of multiple signals.