Evidence map›Paper›PMID 25925327›Full record

ArticleJournal of neurophysiology2015

A highly polarized excitable cell separates sodium channels from sodium-activated potassium channels by more than a millimeter.

Yue Ban, Benjamin E Smith, Michael R Markham

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

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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.

Yue BanDepartment of Biology, The University of Oklahoma, Norman, Oklahoma; Cellular & Behavioral Neurobiology Graduate Program, The University of Oklahoma, Norman, Oklahoma; and yueban@ou.edu.
Benjamin E SmithSamuel Roberts Noble Microscopy Laboratory, The University of Oklahoma, Norman, Oklahoma.
Michael R MarkhamDepartment of Biology, The University of Oklahoma, Norman, Oklahoma; Cellular & Behavioral Neurobiology Graduate Program, The University of Oklahoma, Norman, Oklahoma; and.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bioelectrical properties and resulting metabolic demands of electrogenic cells are determined by their morphology and the subcellular localization of ion channels. The electric organ cells (electrocytes) of the electric fish Eigenmannia virescens generate action potentials (APs) with Na(+) currents >10 μA and repolarize the AP with Na(+)-activated K(+) (KNa) channels. To better understand the role of morphology and ion channel localization in determining the metabolic cost of electrocyte APs, we used two-photon three-dimensional imaging to determine the fine cellular morphology and immunohistochemistry to localize the electrocytes' ion channels, ionotropic receptors, and Na(+)-K(+)-ATPases. We found that electrocytes are highly polarized cells ∼ 1.5 mm in anterior-posterior length and ∼ 0.6 mm in diameter, containing ∼ 30,000 nuclei along the cell periphery. The cell's innervated posterior region is deeply invaginated and vascularized with complex ultrastructural features, whereas the anterior region is relatively smooth. Cholinergic receptors and Na(+) channels are restricted to the innervated posterior region, whereas inward rectifier K(+) channels and the KNa channels that terminate the electrocyte AP are localized to the anterior region, separated by >1 mm from the only sources of Na(+) influx. In other systems, submicrometer spatial coupling of Na(+) and KNa channels is necessary for KNa channel activation. However, our computational simulations showed that KNa channels at a great distance from Na(+) influx can still terminate the AP, suggesting that KNa channels can be activated by distant sources of Na(+) influx and overturning a long-standing assumption that AP-generating ion channels are restricted to the electrocyte's posterior face.

Indexed as

AnimalsBrainComputer SimulationElectric OrganFemaleFish ProteinsGymnotiformesImaging, Three-DimensionalMaleMembrane PotentialsMice, Inbred C57BLModels, NeurologicalPotassium ChannelsSodiumSodium ChannelsSodium-Potassium-Exchanging ATPaseFish ProteinsPotassium ChannelsSodiumSodium ChannelsSodium-Potassium-Exchanging ATPaseaction potential energy efficiencyion channel compartmentalizationsodium-activated potassium channelsthree-dimensional electrolyte morphology

Identifiers

PMID25925327
PMCPMC4509401

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.