Evidence map›Paper›PMID 33537292›Full record

ArticleFrontiers in bioengineering and biotechnology2020

Modulating the Mechanical Activation of TRPV4 at the Cell-Substrate Interface.

Setareh Sianati, Lioba Schroeter, Jessica Richardson, Andy Tay, Shireen R Lamandé, Kate Poole

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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  14. [Research progress of chondrocyte mechanotransduction mediated by TRPV4 and PIEZOs].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2023
    Review
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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

6 authors at 3 institutions in 1 country.

Setareh SianatiEMBL Australia Node in Single Molecule Science and Cellular and Systems Physiology, Faculty of Medicine, School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia.
Lioba SchroeterEMBL Australia Node in Single Molecule Science and Cellular and Systems Physiology, Faculty of Medicine, School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia.
Jessica RichardsonEMBL Australia Node in Single Molecule Science and Cellular and Systems Physiology, Faculty of Medicine, School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia.
Andy TayEMBL Australia Node in Single Molecule Science and Cellular and Systems Physiology, Faculty of Medicine, School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia.
Shireen R LamandéMurdoch Children's Research Institute and Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
Kate PooleEMBL Australia Node in Single Molecule Science and Cellular and Systems Physiology, Faculty of Medicine, School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia.
UNSW Sydney · AUEMBL Australia · AUUniversity of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ion channels activated by mechanical inputs are important force sensing molecules in a wide array of mammalian cells and tissues. The transient receptor potential channel, TRPV4, is a polymodal, nonselective cation channel that can be activated by mechanical inputs but only if stimuli are applied directly at the interface between cells and their substrate, making this molecule a context-dependent force sensor. However, it remains unclear how TRPV4 is activated by mechanical inputs at the cell-substrate interface, which cell intrinsic and cell extrinsic parameters might modulate the mechanical activation of the channel and how mechanical activation differs from TRPV4 gating in response to other stimuli. Here we investigated the impact of substrate mechanics and cytoskeletal components on mechanically evoked TRPV4 currents and addressed how point mutations associated with TRPV4 phosphorylation and arthropathy influence mechanical activation of the channel. Our findings reveal distinct regulatory modulation of TRPV4 from the mechanically activated ion channel PIEZO1, suggesting the mechanosensitivity of these two channels is tuned in response to different parameters. Moreover, our data demonstrate that the effect of point mutations in TRPV4 on channel activation are profoundly dependent on the gating stimulus.

Indexed as

cell-substrate interfacemechanically activated ion channelmechanicsmechanotransductionTRPV4

Identifiers

PMID33537292
PMCPMC7848117
OpenAlexW3122698818

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.