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Creamer, M. S.

Publications and source records attributed to Creamer, M. S..

2 recordsLinked to original sources

Bridging the gap between the connectome and whole-brain activity in C. elegans

A fundamental goal of neuroscience is to understand how anatomy determines the functional properties of the nervous system. However, previous work has failed to show how the functional connections between neurons are derived from the connectome in the nematode C. elegans, raising questions about the extent to which anatomy is informative of signaling1-3. Here, we address this problem using a connectome-constrained dynamical model of the brain, which we fit to whole-brain recordings of neural activity during optogenetic perturbation of single neurons2. This dynamical model, which contains non-zero weights only between anatomically connected neurons, captured causal interactions between all pairs of neurons 82% as well as the reproducibility of the perturbation data themselves. This included interactions between anatomically unconnected neurons, which the model accounted for in terms of signal propagation over paths that include multiple neurons. Strikingly, alternative models fit using a shuffled connectome achieved much lower performance. Finally, we found that adding connections beyond those in the connectome did not improve the models ability to capture causal interactions. Our dynamical model thus provides a link between the connectivity of the C. elegans nervous system and its causal interactions and provides a blueprint for exploring the link between structure and function in other organisms.

neuroscience↗

Long timescale anti-directional rotation in Drosophila optomotor behavior

Locomotor movements cause visual images to be displaced across the eye, a retinal slip that is counteracted by stabilizing reflexes in many animals. In insects, optomotor turning causes the animal to turn in the direction of rotating visual stimuli, thereby reducing retinal slip and stabilizing trajectories through the world. This behavior has formed the basis for extensive dissections of motion vision. Here, we report that under certain stimulus conditions, two Drosophila species, including the widely studied D. melanogaster, can suppress and even reverse the optomotor turning response over several seconds. Such anti-directional turning is most strongly evoked by long-lasting, high-contrast, slow-moving visual stimuli that are distinct from those that promote syn-directional optomotor turning. Anti-directional turning, like the syn-directional optomotor response, requires the local motion detecting neurons T4 and T5. A subset of lobula plate tangential cells, CH cells, show involvement in these responses. Imaging from a variety of direction-selective cells in the lobula plate shows no evidence of dynamics that match the behavior, suggesting that the observed inversion in turning direction emerges downstream of the lobula plate. Further, anti-directional turning declines with age and exposure to light. These results show that Drosophila optomotor turning behaviors contain rich, stimulus-dependent dynamics that are inconsistent with simple reflexive stabilization responses.

neuroscience↗