Interactions between sleep and learning in Drosophila melanogaster: what is the role of PDF target neurons? Understanding the nature and purpose of sleep is currently one of the major goals in neuroscience research. It is clear that sleep is regulated by a combination of circadian and homeostatic systems, and that sleep and memory formation are tightly linked. However, it remains unclear what mechanisms at the circuit and molecular levels mediate these interactions. In the studies proposed here, the powerful Drosophila model system will be used to tackle these issues. It has recently been shown that a cluster of cells once thought to be purely part of the circadian system also play a role in homeostatic sleep regulation. These are the ventral lateral neurons (LNvs), which produce the peptide neurotransmitter PDF. However, it is unknown what the crucial targets of these cells are, or if they are involved in signaling that an organism needs additional sleep following sleep deprivation or learning. By combining genetic manipulations to both increase and decrease the excitability of LNv target cells with cutting edge electrophysiological recordings, this research will expand our understanding of the circuit- and molecular-level strategies that animals use to modulate sleep and memory formation.

Public Health Relevance

(Relevance) Sleep disturbances are highly prevalent in today's society, resulting from shift work, sleep disorders, aging, psychiatric disorders, or simply from an extremely busy lifestyle. Understanding what strategies the brain uses to regulate the amount and quality of sleep that an animal obtains is therefore of urgent importance from a public health standpoint. The proposed research will address this issue by examining the mechanisms used to regulate sleep in response to sleep deprivation and learning experiences.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32MH090711-02
Application #
8107485
Study Section
Special Emphasis Panel (ZRG1-F02A-J (20))
Program Officer
Vogel, Michael W
Project Start
2010-07-01
Project End
2013-06-30
Budget Start
2011-07-01
Budget End
2012-06-30
Support Year
2
Fiscal Year
2011
Total Cost
$51,326
Indirect Cost
Name
Brandeis University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
616845814
City
Waltham
State
MA
Country
United States
Zip Code
02454
Vecsey, Christopher G; Pírez, Nicolás; Griffith, Leslie C (2014) The Drosophila neuropeptides PDF and sNPF have opposing electrophysiological and molecular effects on central neurons. J Neurophysiol 111:1033-45
Shang, Yuhua; Donelson, Nathan C; Vecsey, Christopher G et al. (2013) Short neuropeptide F is a sleep-promoting inhibitory modulator. Neuron 80:171-83
Vecsey, Christopher G; Wimmer, Mathieu E J; Havekes, Robbert et al. (2013) Daily acclimation handling does not affect hippocampal long-term potentiation or cause chronic sleep deprivation in mice. Sleep 36:601-7
Havekes, Robbert; Vecsey, Christopher G; Abel, Ted (2012) The impact of sleep deprivation on neuronal and glial signaling pathways important for memory and synaptic plasticity. Cell Signal 24:1251-60
Vecsey, Christopher G; Peixoto, Lucia; Choi, Jennifer H K et al. (2012) Genomic analysis of sleep deprivation reveals translational regulation in the hippocampus. Physiol Genomics 44:981-91