Sensory Neurons Arouse C. elegans Locomotion via Both Glutamate and Neuropeptide Release.

C. elegans undergoes periods of behavioral quiescence during larval molts (termed lethargus) and as adults. Little is known about the circuit mechanisms that establish these quiescent states. Lethargus and adult locomotion quiescence is dramatically reduced in mutants lacking the neuropeptide recept...

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Main Authors: Seungwon Choi, Kelsey P Taylor, Marios Chatzigeorgiou, Zhitao Hu, William R Schafer, Joshua M Kaplan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-07-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1005359
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author Seungwon Choi
Kelsey P Taylor
Marios Chatzigeorgiou
Zhitao Hu
William R Schafer
Joshua M Kaplan
author_facet Seungwon Choi
Kelsey P Taylor
Marios Chatzigeorgiou
Zhitao Hu
William R Schafer
Joshua M Kaplan
author_sort Seungwon Choi
collection DOAJ
description C. elegans undergoes periods of behavioral quiescence during larval molts (termed lethargus) and as adults. Little is known about the circuit mechanisms that establish these quiescent states. Lethargus and adult locomotion quiescence is dramatically reduced in mutants lacking the neuropeptide receptor NPR-1. Here, we show that the aroused locomotion of npr-1 mutants results from the exaggerated activity in multiple classes of sensory neurons, including nociceptive (ASH), touch sensitive (ALM and PLM), and stretch sensing (DVA) neurons. These sensory neurons accelerate locomotion via both neuropeptide and glutamate release. The relative contribution of these sensory neurons to arousal differs between larval molts and adults. Our results suggest that a broad network of sensory neurons dictates transitions between aroused and quiescent behavioral states.
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spelling doaj-art-e8dae61ccef540a4a08b48caa985cff92025-08-20T03:10:07ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042015-07-01117e100535910.1371/journal.pgen.1005359Sensory Neurons Arouse C. elegans Locomotion via Both Glutamate and Neuropeptide Release.Seungwon ChoiKelsey P TaylorMarios ChatzigeorgiouZhitao HuWilliam R SchaferJoshua M KaplanC. elegans undergoes periods of behavioral quiescence during larval molts (termed lethargus) and as adults. Little is known about the circuit mechanisms that establish these quiescent states. Lethargus and adult locomotion quiescence is dramatically reduced in mutants lacking the neuropeptide receptor NPR-1. Here, we show that the aroused locomotion of npr-1 mutants results from the exaggerated activity in multiple classes of sensory neurons, including nociceptive (ASH), touch sensitive (ALM and PLM), and stretch sensing (DVA) neurons. These sensory neurons accelerate locomotion via both neuropeptide and glutamate release. The relative contribution of these sensory neurons to arousal differs between larval molts and adults. Our results suggest that a broad network of sensory neurons dictates transitions between aroused and quiescent behavioral states.https://doi.org/10.1371/journal.pgen.1005359
spellingShingle Seungwon Choi
Kelsey P Taylor
Marios Chatzigeorgiou
Zhitao Hu
William R Schafer
Joshua M Kaplan
Sensory Neurons Arouse C. elegans Locomotion via Both Glutamate and Neuropeptide Release.
PLoS Genetics
title Sensory Neurons Arouse C. elegans Locomotion via Both Glutamate and Neuropeptide Release.
title_full Sensory Neurons Arouse C. elegans Locomotion via Both Glutamate and Neuropeptide Release.
title_fullStr Sensory Neurons Arouse C. elegans Locomotion via Both Glutamate and Neuropeptide Release.
title_full_unstemmed Sensory Neurons Arouse C. elegans Locomotion via Both Glutamate and Neuropeptide Release.
title_short Sensory Neurons Arouse C. elegans Locomotion via Both Glutamate and Neuropeptide Release.
title_sort sensory neurons arouse c elegans locomotion via both glutamate and neuropeptide release
url https://doi.org/10.1371/journal.pgen.1005359
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