Evidence map›Paper›PMID 17699675›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2007

Dominant-negative inhibition of M-like potassium conductances in hair cells of the mouse inner ear.

Jeffrey R Holt, Eric A Stauffer, David Abraham, Gwenaëlle S G Géléoc

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

44 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The potassium channel subunit KbioRxiv : the preprint server for biology · 2024
    Article
  5. Article
  6. Overlooked KCNQ4 variants augment the risk of hearing loss.Experimental & molecular medicine · 2023
    Article
  7. Article
  8. Article
  9. Signal transmission in mature mammalian vestibular hair cells.Frontiers in cellular neuroscience · 2022
    Article
  10. AGenes · 2021
    Article
  11. Article
  12. Review
  13. Article
  14. Kv7 Channels and Excitability Disorders.Handbook of experimental pharmacology · 2021
    Article
  15. Article
  16. Transcriptomic Analyses of Inner Ear Sensory Epithelia in Zebrafish.Anatomical record (Hoboken, N.J. : 2007) · 2020
    Article
  17. Function and Dysfunction of TMC Channels in Inner Ear Hair Cells.Cold Spring Harbor perspectives in medicine · 2019
    Review
  18. Article
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Jeffrey R HoltDepartment of Neuroscience, University of Virginia, Charlottesville, Virginia 22908, USA. jeffholt@virginia.edu
Eric A Stauffer
David Abraham
Gwenaëlle S G Géléoc
University of Virginia · US

Funding

Ion Channel Function in Auditory & Vestibular Hair CellsR01DC005439 · NIDCD · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI HOLT, JEFFREY R · 2001 to 2019
$5.5M
Ion Channel Function in Auditory & Vestibular Hair CellsR56DC005439 · NIDCD · UNIVERSITY OF VIRGINIA · PI HOLT, JEFFREY R · 2008 to 2008
$379k
Hair cell development in the mouse embryoR03DC006183 · NIDCD · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI GELEOC, GWENAELLE S · 2004 to 2006
$227k
NIDCD NIH HHS DC006183NIDCD NIH HHS DC05439NIDCD NIH HHS R01 DC005439NIDCD NIH HHS R03 DC006183NIDCD NIH HHS R56 DC005439
6 · The paper itself

Abstract

Sensory hair cells of the inner ear express multiple physiologically defined conductances, including mechanotransduction, Ca(2+), Na(+), and several distinct K(+) conductances, all of which are critical for normal hearing and balance function. Yet, the molecular underpinnings and their specific contributions to sensory signaling in the inner ear remain obscure. We sought to identify hair-cell conductances mediated by KCNQ4, which, when mutated, causes the dominant progressive hearing loss DFNA2. We used the dominant-negative pore mutation G285S and packaged the coding sequence of KCNQ4 into adenoviral vectors. We transfected auditory and vestibular hair cells of organotypic cultures generated from the postnatal mouse inner ear. Cochlear outer hair cells and vestibular type I cells that expressed the transfection marker, green fluorescent protein, and the dominant-negative KCNQ4 construct lacked the M-like conductances that typify nontransfected control hair cells. As such, we conclude that the M-like conductances in mouse auditory and vestibular hair cells can include KCNQ4 subunits and may also include KCNQ4 coassembly partners. To examine the function of M-like conductances in hair cells, we recorded from cells transfected with mutant KCNQ4 and injected transduction current waveforms in current-clamp mode. Because the M-like conductances were active at rest, they contributed to the very low potassium-selective input resistance, which in turn hyperpolarized the resting potential and significantly attenuated the amplitude of the receptor potential. Modulation of M-like conductances may allow hair cells the ability to control the amplitude of their response to sensory stimuli.

Indexed as

AnimalsAnimals, NewbornCells, CulturedEar, InnerElectric StimulationEmbryo, MammalianGene ExpressionGene Expression Regulation, DevelopmentalGenetic VectorsGlycineHair Cells, Auditory, InnerHumansKCNQ Potassium ChannelsMembrane PotentialsMiceMutationGlycineKcnq4 protein, mouseKCNQ Potassium ChannelsSerine

Identifiers

PMID17699675
PMCPMC2647843
OpenAlexW1974337436

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.