Evidence map›Paper›PMID 21059759›Full record

ArticleThe Journal of physiology2011

Genetic dissection of ion currents underlying all-or-none action potentials in C. elegans body-wall muscle cells.

Ping Liu, Qian Ge, Bojun Chen, Lawrence Salkoff, Michael I Kotlikoff, Zhao-Wen Wang

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

65 citing papers in PubMed, 103 citations in OpenAlex.

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  11. Increased mitochondrial CaFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
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  13. Regulation of Neurotransmitter Release by KAdvances in neurobiology · 2023
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  16. An extracellular scaffolding complex confers unusual rectification upon an ionotropic acetylcholine receptor inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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5 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Ping LiuDepartment of Neuroscience, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06030-3401, USA.
Qian Ge
Bojun Chen
Lawrence Salkoff
Michael I Kotlikoff
Zhao-Wen Wang
Cornell University · USUConn Health · USWashington University in St. Louis · 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
Transgenic Mice- Recomb., Fate-Mapping,and Ca2+signalingR01DK065992 · NIDDK · CORNELL UNIVERSITY ITHACA · PI KOTLIKOFF, MICHAEL I. · 2004 to 2008
$1.9M
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
Design of Genetically Encoded Ca2+ Indicators for in Vivo ApplicationR01GM086736 · NIGMS · CORNELL UNIVERSITY · PI KOTLIKOFF, MICHAEL I. · 2009 to 2010
$200k
NIDDK NIH HHS 5R01DK065992NIDDK NIH HHS R01 DK065992NIGMS NIH HHS 5R01GM083049NIGMS NIH HHS GM086736NIGMS NIH HHS R01 GM083049NIGMS NIH HHS R01 GM086736NIMH NIH HHS 1R01MH085927NIMH NIH HHS R01 MH085927NINDS NIH HHS R01NS0661871-01
6 · The paper itself

Abstract

Although the neuromuscular system of C. elegans has been studied intensively, little is known about the properties of muscle action potentials (APs). By combining mutant analyses with in vivo electrophysiological recording techniques and Ca2+ imaging, we have established the fundamental properties and molecular determinants of body-wall muscle APs. We show that, unlike mammalian skeletal muscle APs, C. elegans muscle APs occur in spontaneous trains, do not require the function of postsynaptic receptors, and are all-or-none overshooting events, rather than graded potentials as has been previously reported. Furthermore, we show that muscle APs depend on Ca2+ entry through the L-type Ca2+ channel EGL-19 with a contribution from the T-type Ca2+ channel CCA-1. Both the Shaker K+ channel SHK-1 and the Ca2+/Cl−-gated K+ channel SLO-2 play important roles in controlling the speed of membrane repolarization, the amplitude of afterhyperpolarization (AHP) and the pattern of AP firing; SLO-2 is also important in setting the resting membrane potential. Finally, AP-elicited elevations of [Ca2+]i require both EGL-19 and the ryanodine receptor UNC-68. Thus, like mammalian skeletal muscle, C. elegans body-wall myocytes generate all-or-none APs, which evoke Ca2+ release from the sarcoplasmic reticulum (SR), although the specific ion channels used for AP upstroke and repolarization differ.

Indexed as

Action PotentialsAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCalcium ChannelsCalcium Channels, T-TypeExcitation Contraction CouplingIon ChannelsMembrane Transport ProteinsMotor NeuronsMuscle CellsMuscle ProteinsMusclesMutationPatch-Clamp TechniquesRyanodine Receptor Calcium Release ChannelCaenorhabditis elegans ProteinsCalcium ChannelsCalcium Channels, T-TypeEgl-19 protein, C elegansIon ChannelsMembrane Transport ProteinsMuscle ProteinsRyanodine Receptor Calcium Release ChannelShaker Superfamily of Potassium ChannelsSLO-2 protein, C elegansUnc-68 protein, C elegans

Identifiers

PMID21059759
PMCPMC3039263
OpenAlexW2152502422

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.