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Decoding a neural circuit controlling global animal state in C. elegans.

Laurent, Patrick (author)
Soltesz, Zoltan (author)
Nelson, Geoffrey M. (author)
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Chen, Changchun (author)
Laboratory of Molecular Biology, Cambridge, United Kingdom.
Arellano-Carbajal, Fausto (author)
Levy, Emmanuel (author)
de Bono, Mario (author)
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Laboratory of Molecular Biology, Cambridge, United Kingdom (creator_code:org_t)
eLife Sciences Publications, 2015
2015
English.
In: eLIFE. - : eLife Sciences Publications. - 2050-084X. ; 4
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Brains organize behavior and physiology to optimize the response to threats or opportunities. We dissect how 21% O2, an indicator of surface exposure, reprograms C. elegans' global state, inducing sustained locomotory arousal and altering expression of neuropeptides, metabolic enzymes, and other non-neural genes. The URX O2-sensing neurons drive arousal at 21% O2 by tonically activating the RMG interneurons. Stimulating RMG is sufficient to switch behavioral state. Ablating the ASH, ADL, or ASK sensory neurons connected to RMG by gap junctions does not disrupt arousal. However, disrupting cation currents in these neurons curtails RMG neurosecretion and arousal. RMG signals high O2 by peptidergic secretion. Neuropeptide reporters reveal neural circuit state, as neurosecretion stimulates neuropeptide expression. Neural imaging in unrestrained animals shows that URX and RMG encode O2 concentration rather than behavior, while the activity of downstream interneurons such as AVB and AIY reflect both O2 levels and the behavior being executed.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Keyword

C. elegans
TRPV
caenorhabditis
gap junctions
neural circuit
neuroscience
optogenetics

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ref (subject category)
art (subject category)

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