Connectomic features underlying diverse synaptic connection strengths and subcellular computation

Connectomes generated from electron microscopy images of neural tissue unveil the complex morphology of every neuron and the locations of every synapse interconnecting them. These wiring diagrams may also enable inference of synaptic and neuronal biophysics, such as the functional weights of synaptic connections, but this requires integration with physiological data to properly parameterize. Working with a stereotyped olfactory network in the Drosophila brain, we make direct comparisons of the anatomy and physiology of diverse neurons and synapses with subcellular and subthreshold resolution. We find that synapse density and location jointly predict the amplitude of the somatic postsynaptic potential evoked by a single presynaptic spike. Biophysical models fit to data predict that electrical compartmentalization allows axon and dendrite arbors to balance independent and interacting computations. These findings begin to fill the gap between connectivity maps and activity maps, which should enable new hypotheses about how network structure constrains network function.

Automated summary

Connectomes generated from electron microscopy images of neural tissue can reveal the complex morphology and synaptic locations in a neural network. Research has shown that the density and location of synapses can predict the amplitude of postsynaptic potentials. Biophysical models predict that electrical compartmentalization allows for balanced computations between axon and dendritic arbors.