Evidence map›Paper›PMID 35159201›Full record

ArticleCells2022

Fine-Tuning of Piezo1 Expression and Activity Ensures Efficient Myoblast Fusion during Skeletal Myogenesis.

Huascar Pedro Ortuste Quiroga, Massimo Ganassi, Shingo Yokoyama, Kodai Nakamura, Tomohiro Yamashita, Daniel Raimbach, Arisa Hagiwara, Oscar Harrington, Jodie Breach-Teji, Atsushi Asakura and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact, top 100% 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

29 citing papers in PubMed, 0 citations in OpenAlex.

  1. PIEZO1 Mediates Myoblast Proliferation Under Simulated Microgravity.Annals of the New York Academy of Sciences · 2026
    Article
  2. Review
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  7. Lipid Regulation of Mechanosensitive Ion Channels.International journal of molecular sciences · 2026
    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

14 authors at 4 institutions in 3 countries.

Huascar Pedro Ortuste QuirogaDepartment of Physiology, Graduate School of Health Sciences, Toyohashi SOZO University, Aichi, Toyohashi 440-0016, Japan.
Massimo GanassiRandall Centre for Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK.
Shingo YokoyamaLaboratory of Physiology, School of Health Sciences, Toyohashi SOZO University, Aichi, Toyohashi 440-0016, Japan.
Kodai NakamuraDepartment of Physiology, Graduate School of Health Sciences, Toyohashi SOZO University, Aichi, Toyohashi 440-0016, Japan.
Tomohiro YamashitaDepartment of Physiology, Graduate School of Health Sciences, Toyohashi SOZO University, Aichi, Toyohashi 440-0016, Japan.
Daniel RaimbachCentre of Human and Aerospace Physiological Sciences, King's College London, London SE1 1UL, UK.
Arisa HagiwaraDepartment of Physiology, Graduate School of Health Sciences, Toyohashi SOZO University, Aichi, Toyohashi 440-0016, Japan.
Oscar HarringtonCentre of Human and Aerospace Physiological Sciences, King's College London, London SE1 1UL, UK.
Jodie Breach-TejiCentre of Human and Aerospace Physiological Sciences, King's College London, London SE1 1UL, UK.
Atsushi AsakuraPaul & Sheila Wellstone Muscular Dystrophy Center, Department of Neurology, Stem Cell Institute, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
Yoshiro SuzukiDivision of Cell Signalling, National Institute for Physiological Sciences, Aichi, Okazaki 444-0864, Japan.ORCID 0000-0003-0010-1867
Makoto TominagaDivision of Cell Signalling, National Institute for Physiological Sciences, Aichi, Okazaki 444-0864, Japan.
Peter S ZammitRandall Centre for Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK.
Katsumasa GotoDepartment of Physiology, Graduate School of Health Sciences, Toyohashi SOZO University, Aichi, Toyohashi 440-0016, Japan.ORCID 0000-0001-5380-4561
Toyohashi Sozo College · JPKing's College London · GBNational Institute for Physiological Sciences · JPUniversity of Minnesota · US

Funding

KAKENHI 19KK0254KAKENHI JP17K01762KAKENHI JP18H03160KAKENHI JP19K22825Medical Research Council MR/S002472/1National Institute of Health Sciences AR078400Regenerative Medicine Minnesota (RMM) 092319 TR010
6 · The paper itself

Abstract

Mechanical stimuli, such as stretch and resistance training, are essential in regulating the growth and functioning of skeletal muscles. However, the molecular mechanisms involved in sensing mechanical stress during muscle formation remain unclear. Here, we investigated the role of the mechanosensitive ion channel Piezo1 during myogenic progression of both fast and slow muscle satellite cells. We found that Piezo1 level increases during myogenic differentiation and direct manipulation of Piezo1 in muscle stem cells alters the myogenic progression. Indeed, Piezo1 knockdown suppresses myoblast fusion, leading to smaller myotubes. Such an event is accompanied by significant downregulation of the fusogenic protein

Indexed as

Muscle DevelopmentMyoblastsCell CommunicationCell DifferentiationMuscle Fibers, SkeletalCa2+ channelFam38Agrowthmechanosensationmyoblast fusionmyogenesisPiezo1satellite cellsskeletal muscle

Identifiers

PMID35159201
PMCPMC8834081
OpenAlexW3217342144

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.