Heterogeneous synaptic motifs bridge microscale structure and macroscale nonlinear dynamics
Organizations: Center for Quantitative Biology, Academy for Advanced Interdisciplinary Studies, Peking University, China · Center for Quantitative Biology, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China · School of Physics, Peking University, China · School of Physics, Peking University, Beijing, China · Center for Bioinformatics, National Laboratory of Protein Engineering and Plant Genetic Engineering, Peking University, China · School of Life Sciences, Peking University, China · Center for Bioinformatics, National Laboratory of Protein Engineering and Plant Genetic Engineering, School of Life Sciences and Center for Quantitative Biology, Academy for Advanced Interdisciplinary Studies,Peking University, Beijing, China · Laboratoire Jean Alexandre Dieudonne, Universite Cote dAzur, France · Neuromod Institute, Universite Cote dAzur, France · Laboratoire Jean Alexandre Dieudonné, Neuromod Institute, Universit´e Cˆote d’Azur, Nice, France
Abstract
Recent breakthroughs in synaptic-resolution network connectomics have revealed that brain circuits feature fine-scale structural connectivity, such as pairs of correlated synaptic couplings known as second-order motifs. Large-scale recordings of neuronal activity in networks containing nonlinear neurons reveal macroscopic heterogeneous population dynamics throughout the brain. These findings rekindle the inquiry into this intriguing question: Can microscale synaptic structures contribute to macroscopic heterogeneous dynamics and computations in ways that canonical brain circuit models cannot? To answer this question, we create random RNNs with various cell types, nonlinear non-negative neural responses, and arbitrary marginal and second-order correlated synaptic statistics. We derive mean-field low-rank equations for P-population networks in which the pre- and postsynaptic neuronal population identities determine the synaptic and motif strengths. Our framework requires 2P latent dynamic variables with P variables describing mean population activity and P variables capturing within-population variability. Theoretical and simulational results demonstrate that chain motifs induce correlations in synaptic variability, enabling microscopic fluctuations to be integrated and influence mesoscopic mean population dynamics. We apply this framework to reverse engineer network connectivity that recapitulates the heterogeneous activity across the population in the mouse primary visual cortex. By bridging the gap between synaptic organization and nonlinear heterogeneous population dynamics, our results offer a principled approach and testable predictions regarding the relationship between fine-scale connectivity, heterogeneous dynamics, and functional computations.