Evidence map›Paper›PMID 25961826›Full record

ArticlePloS one2015

Channel properties of Nax expressed in neurons.

Masahito Matsumoto, Takeshi Y Hiyama, Kazuya Kuboyama, Ryoko Suzuki, Akihiro Fujikawa, Masaharu Noda

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Structure-guided unlocking of NaNature communications · 2022
    Article
  4. Central regulation of body fluid homeostasis.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2022
    Review
  5. The NaCellular and molecular life sciences : CMLS · 2021
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. NaAnnals of translational medicine · 2016
    Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Masahito MatsumotoDivision of Molecular Neurobiology, National Institute for Basic Biology, Okazaki, Japan.
Takeshi Y HiyamaDivision of Molecular Neurobiology, National Institute for Basic Biology, Okazaki, Japan; School of Life Science, SOKENDAI (The Graduate University for Advanced Studies), Okazaki, Japan.
Kazuya KuboyamaDivision of Molecular Neurobiology, National Institute for Basic Biology, Okazaki, Japan.
Ryoko SuzukiDivision of Molecular Neurobiology, National Institute for Basic Biology, Okazaki, Japan.
Akihiro FujikawaDivision of Molecular Neurobiology, National Institute for Basic Biology, Okazaki, Japan.
Masaharu NodaDivision of Molecular Neurobiology, National Institute for Basic Biology, Okazaki, Japan; School of Life Science, SOKENDAI (The Graduate University for Advanced Studies), Okazaki, Japan.
National Institute for Basic Biology · JPThe Graduate University for Advanced Studies, SOKENDAI · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nax is a sodium-concentration ([Na+])-sensitive Na channel with a gating threshold of ~150 mM for extracellular [Na+] ([Na+]o) in vitro. We previously reported that Nax was preferentially expressed in the glial cells of sensory circumventricular organs including the subfornical organ, and was involved in [Na+] sensing for the control of salt-intake behavior. Although Nax was also suggested to be expressed in the neurons of some brain regions including the amygdala and cerebral cortex, the channel properties of Nax have not yet been adequately characterized in neurons. We herein verified that Nax was expressed in neurons in the lateral amygdala of mice using an antibody that was newly generated against mouse Nax. To investigate the channel properties of Nax expressed in neurons, we established an inducible cell line of Nax using the mouse neuroblastoma cell line, Neuro-2a, which is endogenously devoid of the expression of Nax. Functional analyses of this cell line revealed that the [Na+]-sensitivity of Nax in neuronal cells was similar to that expressed in glial cells. The cation selectivity sequence of the Nax channel in cations was revealed to be Na+ ≈ Li+ > Rb+ > Cs+ for the first time. Furthermore, we demonstrated that Nax bound to postsynaptic density protein 95 (PSD95) through its PSD95/Disc-large/ZO-1 (PDZ)-binding motif at the C-terminus in neurons. The interaction between Nax and PSD95 may be involved in promoting the surface expression of Nax channels because the depletion of endogenous PSD95 resulted in a decrease in Nax at the plasma membrane. These results indicated, for the first time, that Nax functions as a [Na+]-sensitive Na channel in neurons as well as in glial cells.

Indexed as

AmygdalaAnimalsCell LineCells, CulturedImmunohistochemistryMiceNeuronsRatsSodiumVoltage-Gated Sodium ChannelsSodiumVoltage-Gated Sodium Channels

Identifiers

PMID25961826
PMCPMC4427406
OpenAlexW2336854900

What OpenQuestion holds

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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.