Temporal signals drive the emergence of multicellular information networks
arXiv:2202.13462 · doi:10.1073/pnas.2202204119
Abstract
Coordinated responses to environmental stimuli are critical for multicellular organisms. To overcome the obstacles of cell-to-cell heterogeneity and noisy signaling dynamics within individual cells, cells must effectively exchange information with peers. However, the dynamics and mechanisms of collective information transfer driven by external signals is poorly understood. Here we investigate the calcium dynamics of neuronal cells that form confluent monolayers and respond to cyclic ATP stimuli in microfluidic devices. Using Granger inference to reconstruct the underlying causal relations between the cells, we find that the cells self-organize into spatially decentralized and temporally stationary networks to support information transfer via gap junction channels. The connectivity of the causal networks depend on the temporal profile of the external stimuli, where short periods, or long periods with small duty fractions, lead to reduced connectivity and fractured network topology. We build a theoretical model based on communicating excitable units that reproduces our observations. The model further predicts that connectivity of the causal network is maximal at an optimal communication strength, which is confirmed by the experiments. Together, our results show that information transfer between neuronal cells is externally regulated by the temporal profile of the stimuli, and internally regulated by cell-cell communication.
arXiv comment27 pages, 19 figures
References in corpus (7)
- Granger causality and transfer entropy are equivalent for Gaussian variables
- Broken detailed balance and entropy production in the human brain
- Cell-cell communication enhances the capacity of cell ensembles to sense shallow gradients during morphogenesis
- Maximum likelihood and the single receptor
- Communication shapes sensory response in multicellular networks
- Universality of biochemical feedback and its application to immune cells
- Cell-to-cell information at a feedback-induced bifurcation point