Analysis of NPR-1 reveals a circuit mechanism for behavioral quiescence in C. elegans

Neuron. 2013 Jun 5;78(5):869-80. doi: 10.1016/j.neuron.2013.04.002.

Abstract

Animals undergo periods of behavioral quiescence and arousal in response to environmental, circadian, or developmental cues. During larval molts, C. elegans undergoes a period of profound behavioral quiescence termed lethargus. Locomotion quiescence during lethargus was abolished in mutants lacking a neuropeptide receptor (NPR-1) and was reduced in mutants lacking NPR-1 ligands (FLP-18 and FLP-21). Wild-type strains are polymorphic for the npr-1 gene, and their lethargus behavior varies correspondingly. Locomotion quiescence and arousal were mediated by decreased and increased secretion of an arousal neuropeptide (PDF-1) from central neurons. PDF receptors (PDFR-1) expressed in peripheral mechanosensory neurons enhanced touch-evoked calcium transients. Thus, a central circuit stimulates arousal from lethargus by enhancing the sensitivity of peripheral mechanosensory neurons in the body. These results define a circuit mechanism controlling a developmentally programmed form of quiescence.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Video-Audio Media

MeSH terms

  • Age Factors
  • Animals
  • Animals, Genetically Modified
  • Arousal / genetics*
  • Behavior, Animal / drug effects
  • Behavior, Animal / physiology*
  • Caenorhabditis elegans
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • Capsaicin / pharmacology
  • Central Nervous System / cytology
  • Larva
  • Lethargy / genetics*
  • Locomotion / drug effects
  • Locomotion / genetics*
  • Muscles / metabolism
  • Mutation / genetics
  • Receptors, Neuropeptide Y / genetics
  • Receptors, Neuropeptide Y / metabolism*
  • Sensory Receptor Cells / drug effects
  • Sensory Receptor Cells / physiology
  • TRPV Cation Channels
  • Touch / genetics
  • gamma-Aminobutyric Acid / metabolism

Substances

  • Caenorhabditis elegans Proteins
  • NPR-1 protein, C elegans
  • Receptors, Neuropeptide Y
  • TRPV Cation Channels
  • Trpv1 protein, rat
  • gamma-Aminobutyric Acid
  • Capsaicin