Evidence map›Paper›PMID 22033926›Full record

ArticleThe Journal of biological chemistry2011

Gap junctions synchronize action potentials and Ca2+ transients in Caenorhabditis elegans body wall muscle.

Ping Liu, Bojun Chen, Zhao-Wen Wang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.5field-weighted citation impact, top 43% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  10. Review
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  12. Illuminating neural circuits and behaviour in Caenorhabditis elegans with optogenetics.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Review
  13. Neurobiology ofBioscience · 2014
    Article
  14. Gap junctions in C. elegans.Frontiers in physiology · 2014
    Review
  15. CLHM-1 is a functionally conserved and conditionally toxic Ca2+-permeable ion channel in Caenorhabditis elegans.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  16. Article
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Ping LiuDepartment of Neuroscience, University of Connecticut Health Center, Farmington, Connecticut 06030.
Bojun ChenDepartment of Neuroscience, University of Connecticut Health Center, Farmington, Connecticut 06030.
Zhao-Wen WangDepartment of Neuroscience, University of Connecticut Health Center, Farmington, Connecticut 06030. Electronic address: zwwang@uchc.edu.
UConn Health · US

Funding

Synaptic function of BK channel-interacting proteinsR01MH085927 · NIMH · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ZHAO-WEN WANG · 2010 to 2026
$6.7M
Regulation of gap junctions by stomatin-like proteinsR01GM083049 · NIGMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI WANG, ZHAO-WEN · 2008 to 2012
$1.5M
REGULATION OF CALCIUM ACTIVATED POTASSIUM CHANNELSF32HL009294 · NHLBI · WASHINGTON UNIVERSITY · PI WANG, ZHAO-WEN · 1995 to 1998
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NHLBI NIH HHS F32 HL009294NIGMS NIH HHS 5R01GM083049NIGMS NIH HHS R01 GM083049NIMH NIH HHS 1R01MH085927NIMH NIH HHS R01 MH085927
6 · The paper itself

Abstract

The sinusoidal locomotion of Caenorhabditis elegans requires synchronous activities of neighboring body wall muscle cells. However, it is unknown whether the synchrony results from muscle electrical coupling or neural inputs. We analyzed the effects of mutating gap junction proteins and blocking neuromuscular transmission on the synchrony of action potentials (APs) and Ca2+ transients among neighboring body wall muscle cells. In wild-type worms, the percentage of synchronous APs between two neighboring cells varied depending on the anatomical relationship and junctional conductance (Gj) between them, and Ca2+ transients were synchronous among neighboring muscle cells. Compared with the wild type, knock-out of the gap junction gene unc-9 resulted in greatly reduced coupling coefficient and asynchronous APs and Ca2+ transients. Inhibition of unc-9 expression specifically in muscle by RNAi also reduced the synchrony of APs and Ca2+ transients, whereas expression of wild-type UNC-9 specifically in muscle rescued the synchrony defect. Loss of the stomatin-like protein UNC-1, which is a regulator of UNC-9-based gap junctions, similarly impaired muscle synchrony as unc-9 mutant did. The blockade of muscle ionotropic acetylcholine receptors by (+)-tubocurarine decreased the frequencies of APs and Ca2+ transients, whereas blockade of muscle GABAA receptors by gabazine had opposite effects. However, both APs and Ca2+ transients remained synchronous after the application of (+)-tubocurarine and/or gabazine. These observations suggest that gap junctions in C. elegans body wall muscle cells are responsible for synchronizing muscle APs and Ca2+ transients.

Indexed as

Action PotentialsAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCalciumCalcium SignalingElectrophysiologyGap JunctionsModels, BiologicalMusclesNeuromuscular Nondepolarizing AgentsPyridazinesRNA InterferenceSynaptic TransmissionTubocurarineCaenorhabditis elegans ProteinsCalciumgabazineNeuromuscular Nondepolarizing AgentsPyridazinesTubocurarine

Identifiers

PMID22033926
PMCPMC3243499
OpenAlexW2002186730

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.