Published January 16, 2014 | Version Accepted Version
Journal Article Open

Multilevel Modulation of a Sensory Motor Circuit during C. elegans Sleep and Arousal

  • 1. ROR icon California Institute of Technology

Abstract

Sleep is characterized by behavioral quiescence, homeostasis, increased arousal threshold, and rapid reversibility. Understanding how these properties are encoded by a neuronal circuit has been difficult, and no single molecular or neuronal pathway has been shown to be responsible for the regulation of sleep. Taking advantage of the well-mapped neuronal connections of Caenorhabditis elegans and the sleep-like states in this animal, we demonstrate the changed properties of both sensory neurons and downstream interneurons that mediate sleep and arousal. The ASH sensory neuron displays reduced sensitivity to stimuli in the sleep-like state, and the activity of the corresponding interneurons in ASH's motor circuit becomes asynchronous. Restoration of interneuron synchrony is sufficient for arousal. The multilevel circuit depression revealed provides an elegant strategy to promote a robust decrease in arousal while allowing for rapid reversibility of the sleep state.

Additional Information

© 2014 Elsevier Inc. Received: May 25, 2013; Revised: September 26, 2013; Accepted: November 15, 2013; Published: January 16, 2014. We thank William Schafer (University of Cambridge), Alexander Gottschalk (Johann Wolfgang Goethe University), Elissa Hallem (University of California, Los Angeles), and the Caenorhabditis Genetics Center (University of Minnesota) for worm strains and Karl Deisseroth (Stanford University) for channelrhodopsin constructs. We also thank David Anderson, David Prober, Alon Zaslaver, Trevor Fowler, and Lauren Lebon for their input and Meenakshi Doma, Yen-ping Hsueh, Mihoko Kato, Hillel Schwartz, and members of our lab for editorial comments. J.Y.C. was supported by National Institutes of Health USPHS training grant GM07616. This work was supported by the Howard Hughes Medical Institute, with which P.W.S. is an investigator, and by NIH grant DA018341 to P.W.S.

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Additional details

Identifiers

PMCID
PMC3962823
Eprint ID
43481
Resolver ID
CaltechAUTHORS:20140123-085452909

Funding

NIH USPHS Training Grant
GM07616
Howard Hughes Medical Institute (HHMI)
NIH
DA018341

Dates

Created
2014-01-23
Created from EPrint's datestamp field
Updated
2021-11-10
Created from EPrint's last_modified field