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Castillo, L. M. P.

Publications and source records attributed to Castillo, L. M. P..

2 recordsLinked to original sources

Electrical synapses mediate visual approach behavior

Detecting salient visual objects and orienting toward them are commonplace tasks for animals, yet the underlying neural circuits remain poorly understood. The fruit fly is an ideal model for a comprehensive analysis of feature detection mechanisms given its complete synaptic wiring diagrams, robust behavioral assays, and cell-type-specific gene expression datasets. We previously showed that columnar T3 neurons are required for saccadic orientation toward landscape features during flight. Here, we examine how signals downstream of T3 are processed in the central brain. We identify LC17 visual projection neurons as key postsynaptic targets: they receive strong excitatory input from T3, project to premotor brain regions, and are thus positioned to support visual approach. Using in vivo optical physiology and virtual reality behavior, we demonstrate that LC17 neurons are indeed necessary for object tracking during flight. Furthermore, we find that electrical synapses in LC17 are also required for tracking behavior. We show that the innexin Shaking B (shakB) is highly expressed in LC17 and localized to its dendrites, and genetic perturbations confirm its essential role for electrical coupling in this circuit. Our findings reveal mechanisms underlying visual approach, and highlight the interplay between electrical and chemical neurotransmission for rapid object detection and action selection.

neuroscience↗

Four neurons pattern brain-wide developmental activity through neuropeptide signaling.

The developing brain becomes electrically active before it is ready to process sensory input. During neural circuit maturation, developmental activity is thought to refine synaptic connections by driving neuronal co-activation in rhythmic patterns. The source of this brainwide activity and the mechanisms which regulate its patterns are not well understood. Here we describe cellular interactions that shape developmental activity and their molecular basis. In Drosophila, patterned stimulus independent neural activity (PSINA) engages the entire brain in highly stereotyped, globally coordinated cycles of activity. A molecularly-defined population of [~]2,000 neurons (Transient Receptor Potential Gamma, Trp{gamma}+ neurons) act as an activity template for PSINA. We show that this activity template is patterned by four neurons expressing the neuropeptide SIFamide (SIFa). Signaling through the SIFa Receptor, SIFa modulates the activity of both SIFa and Trp{gamma}+ neurons to establish the brainwide activity cycles of PSINA. In turn, Trp{gamma}+ neurons regulate SIFa neuron activity through a recurrent interaction. Neuropeptides act through synapse-free, or wireless, signaling; a fitting mode of communication for a process tasked with refining on-going synapse formation. By placing neuropeptide signaling at the core of developmental activity, this work highlights the rich neurophysiological potential of the chemical connectome in shaping the developing brain.

neuroscience↗