Evidence map›Paper›PMID 25409445›Full record

ArticlePloS one2014

Fine Tuning of CaV1.3 Ca2+ channel properties in adult inner hair cells positioned in the most sensitive region of the Gerbil Cochlea.

Valeria Zampini, Stuart L Johnson, Christoph Franz, Marlies Knipper, Matthew C Holley, Jacopo Magistretti, Giancarlo Russo, Walter Marcotti, Sergio Masetto

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Purinergic Signaling Controls Spontaneous Activity in the Auditory System throughout Early Development.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  4. Review
  5. Review
  6. Article
  7. 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

9 authors at 3 institutions in 3 countries.

Valeria ZampiniDepartment of Biomedical Science, University of Sheffield, Sheffield, United Kingdom; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Stuart L JohnsonDepartment of Biomedical Science, University of Sheffield, Sheffield, United Kingdom.
Christoph FranzDepartment of Otolaryngology, Tübingen Hearing Research Centre, Laboratory of Molecular Physiology of Hearing, University of Tübingen, Tübingen, Germany.
Marlies KnipperDepartment of Otolaryngology, Tübingen Hearing Research Centre, Laboratory of Molecular Physiology of Hearing, University of Tübingen, Tübingen, Germany.
Matthew C HolleyDepartment of Biomedical Science, University of Sheffield, Sheffield, United Kingdom.
Jacopo MagistrettiDepartment of Biology and Biotechnology "Lazzaro Spallanzani", University of Pavia, Pavia, Italy.
Giancarlo RussoDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Walter MarcottiDepartment of Biomedical Science, University of Sheffield, Sheffield, United Kingdom.
Sergio MasettoDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
University of Sheffield · GBUniversity of Pavia · ITUniversity of Tübingen · DE

Funding

Wellcome TrustWellcome Trust 091895
6 · The paper itself

Abstract

Hearing relies on faithful signal transmission by cochlear inner hair cells (IHCs) onto auditory fibres over a wide frequency and intensity range. Exocytosis at IHC ribbon synapses is triggered by Ca(2+) inflow through Ca(V)1.3 (L-type) Ca(2+) channels. We investigated the macroscopic (whole-cell) and elementary (cell-attached) properties of Ca(2+) currents in IHCs positioned at the middle turn (frequency ∼ 2 kHz) of the adult gerbil cochlea, which is their most sensitive hearing region. Using near physiological recordings conditions (body temperature and a Na(+) based extracellular solution), we found that the macroscopic Ca(2+) current activates and deactivates very rapidly (time constant below 1 ms) and inactivates slowly and only partially. Single-channel recordings showed an elementary conductance of 15 pS, a sub-ms latency to first opening, and a very low steady-state open probability (Po: 0.024 in response to 500-ms depolarizing steps at ∼-18 mV). The value of Po was significantly larger (0.06) in the first 40 ms of membrane depolarization, which corresponds to the time when most Ca(2+) channel openings occurred clustered in bursts (mean burst duration: 19 ms). Both the Po and the mean burst duration were smaller than those previously reported in high-frequency basal IHCs. Finally, we found that middle turn IHCs are likely to express about 4 times more Ca(2+) channels per ribbon than basal cells. We propose that middle-turn IHCs finely-tune Ca(V)1.3 Ca(2+) channel gating in order to provide reliable information upon timing and intensity of lower-frequency sounds.

Indexed as

AnimalsCalcium Channels, L-TypeCochleaExocytosisGerbillinaeHair Cells, Auditory, InnerImmunohistochemistryIonsMembrane PotentialsPatch-Clamp TechniquesSodiumSynapsesCacna1d protein, mouseCalcium Channels, L-TypeIonsSodium

Identifiers

PMID25409445
PMCPMC4237458
OpenAlexW2014499707

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.