Sophie Dvali | Searcharxiv

arXiv2025

Diverging network architecture of the $\textit{C. elegans}$ connectome and signaling network

The connectome describes the complete set of synaptic contacts through which neurons communicate. While the architecture of the $\textit{C. elegans}$ connectome has been extensively characterized, much less is known about the organization of causal signaling networks arising from functional interactions between neurons. Understanding how effective communication pathways relate to or diverge from the underlying structure is a central question in neuroscience. Here, we analyze the modular architecture of the $\textit{C. elegans}$ signal propagation network, measured via calcium imaging and optogenetics, and compare it to the underlying anatomical wiring measured by electron microscopy. Compared to the connectome, we find that signaling modules are not aligned with the modular boundaries of the anatomical network, highlighting an instance where function deviates from structure. However, we find that some of the most striking features of the anatomical network are preserved, as exemplified by the pharynx, which is delineated into a separate community in both anatomy and signaling. We analyze the cellular compositions of the signaling architecture and find that its modules are enriched for specific cell types and functions, suggesting that the network modules are neurobiologically relevant. Lastly, we identify a "rich club" of hub neurons in the signaling network. The membership of the signaling rich club differs from the rich club detected in the anatomical network, challenging the view that structural hubs occupy positions of influence in functional (signaling) networks. Our results provide new insight into the interplay between brain structure, in the form of a complete synaptic-level connectome, and brain function, in the form of a system-wide causal signal propagation atlas.

q-bio.NC↗

arXiv2023

Neural signal propagation atlas of C. elegans

A fundamental problem in neuroscience is understanding how a network's properties dictate its function. Connectomics provides one avenue to predict nervous system function. To test this explicitly, we systematically measure signal propagation in 23,427 pairs of neurons across the head of the nematode Caenorhabditis elegans by direct optogenetic activation and simultaneous whole-brain calcium imaging. We measure the sign (excitatory or inhibitory), strength, temporal properties, and causal direction of signal propagation between these neurons to create a functional atlas. We find that signal propagation differs from predictions based on anatomy. Using mutants, we show that extrasynaptic signaling not visible from anatomy contributes to this difference. We identify many instances of dense-core-vesicle dependent signaling on seconds-or-less timescales that evoke acute calcium transients often where no direct wired connection exists but where relevant neuropeptides and receptors are expressed. We propose that here extrasynaptically released neuropeptides serve a similar function as that of classical neurotransmitters. Finally, our measured signal propagation atlas better predicts neural dynamics of spontaneous activity than does anatomy. We conclude that both synaptic and extrasynaptic signaling drive neural dynamics on short timescales and that measurement of evoked signal propagation are critical for interpreting neural function.

q-bio.NC↗