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Dopp, J.

Publications and source records attributed to Dopp, J..

2 recordsLinked to original sources

Genetic targeting of astrocytes associated with specific neuronal circuit in adult Drosophila

Astrocytes are the major glial population of the brain and have been associated with a vast number of functions. To probe this diversity and to reach a similar level of understanding about astrocyte physiology that we have about neurons, we need genetic tools to target specific astrocytic subpopulations. In Drosophila, we are restricted to using driver lines that drive expression in astrocytes throughout the brain. To target specific astrocytes, we have optimized the genetic tool TRACT (and refer to it as astro-TRACT), allowing effector expression specifically in local astrocytes of a given neuronal circuit. We analyzed specificity, sensitivity and reproducibility of the tool across various MB split-Gal4 drivers. We found that the number of pre-synapses correlates positively with the success of the tool. Applying the tool to characterize morphology of individual astrocytes revealed that local astrocytes around MB medial compartments project into the ellipsoid body. Astro-TRACT will be a valuable resource to investigate both mechanistic astrocyte-neuron signaling and functional and structural astrocytic diversity across the adult Drosophila brain.

neuroscience↗

Single-cell transcriptomics reveals that glial cells integrate homeostatic and circadian processes to drive sleep-wake cycles

The sleep-wake cycle is determined by circadian and sleep homeostatic processes. However, the molecular impact of these processes and their interaction in different brain cell populations remain unknown. To fill this gap, we profiled the single-cell transcriptome of adult Drosophila brains across the sleep-wake cycle and four circadian times. We show cell type-specific transcriptomic changes with glia displaying the largest variation. Glia are also among the few cell types whose gene expression correlates with both sleep homeostat and circadian clock. The sleep-wake cycle and sleep drive level affect expression of clock gene regulators in glia, while diminishing the circadian clock specifically in glia impairs homeostatic sleep rebound after sleep deprivation. These findings reveal a comprehensive view of the effects of sleep homeostatic and circadian processes on distinct cell types in an entire animal brain and reveal glia as an interaction site of these two processes to determine sleep-wake dynamics.

animal behavior and cognition↗