Evidence map›Paper›PMID 32186512›Full record

ArticleeLife2020

Piezo1/2 mediate mechanotransduction essential for bone formation through concerted activation of NFAT-YAP1-ß-catenin.

Taifeng Zhou, Bo Gao, Yi Fan, Yuchen Liu, Shuhao Feng, Qian Cong, Xiaolei Zhang, Yaxing Zhou, Prem S Yadav, Jiachen Lin and 6 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 242 papers.

0numbers the graph read from it
0cells of the map it votes in
242citing papers in PubMed
19.1field-weighted citation impact, top 1% 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

242 citing papers in PubMed, 339 citations in OpenAlex.

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182 more citing papers are in PubMed but not listed here.

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

16 authors at 5 institutions in 2 countries.

Taifeng ZhouDepartment of Developmental Biology, Harvard School of Dental Medicine, Harvard Stem Cell Institute, Boston, United States.
Bo GaoDepartment of Developmental Biology, Harvard School of Dental Medicine, Harvard Stem Cell Institute, Boston, United States.
Yi FanDepartment of Developmental Biology, Harvard School of Dental Medicine, Harvard Stem Cell Institute, Boston, United States.
Yuchen LiuDepartment of Developmental Biology, Harvard School of Dental Medicine, Harvard Stem Cell Institute, Boston, United States.
Shuhao FengDepartment of Developmental Biology, Harvard School of Dental Medicine, Harvard Stem Cell Institute, Boston, United States.
Qian CongDepartment of Developmental Biology, Harvard School of Dental Medicine, Harvard Stem Cell Institute, Boston, United States.
Xiaolei ZhangDepartment of Developmental Biology, Harvard School of Dental Medicine, Harvard Stem Cell Institute, Boston, United States.
Yaxing ZhouDepartment of Developmental Biology, Harvard School of Dental Medicine, Harvard Stem Cell Institute, Boston, United States.
Prem S YadavDepartment of Developmental Biology, Harvard School of Dental Medicine, Harvard Stem Cell Institute, Boston, United States.
Jiachen LinDepartment of Developmental Biology, Harvard School of Dental Medicine, Harvard Stem Cell Institute, Boston, United States.
Nan WuDepartment of Orthopedic Surgery and Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.ORCID 0000-0002-9429-2889
Liang ZhaoDepartment of Orthopedic Surgery, Nanfang Hospital, Southern Medical University, Guangdong, China.
Dongsheng HuangDepartment of Spine Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Shuanhu ZhouDepartment of Orthopedic Surgery, Brigham and Women's Hospital, Boston, United States.
Peiqiang SuDepartment of Orthopaedic Surgery, Guangdong Provincial Key Laboratory of Orthopedics and Traumatology, First Affiliated Hospital of Sun Yat-sen University, Sun Yat-sen University, Guangzhou, China.
Yingzi YangDepartment of Developmental Biology, Harvard School of Dental Medicine, Harvard Stem Cell Institute, Boston, United States.ORCID 0000-0003-3933-887X
Harvard Stem Cell Institute · USSun Yat-sen University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNNanfang Hospital · CNBrigham and Women's Hospital · US

Funding

Gas-Hedgehog signaling in intramembranous bone formation and expansionR01DE025866 · NIDCR · HARVARD MEDICAL SCHOOL · PI Yingzi Yang · 2016 to 2026
$5.3M
Molecular Mechanism of Wnt/Planar Cell Polarity SignalingR01AR070877 · NIAMS · HARVARD MEDICAL SCHOOL · PI YANG, YINGZI · 2017 to 2022
$3.0M
Cellular and molecular mechanism of Hippo signaling in suppressing liver tumor formationR01CA222571 · NCI · HARVARD MEDICAL SCHOOL · PI YANG, YINGZI · 2018 to 2022
$1.9M
China Scholarship Council 201806210436China Scholarship Council 201806380049NCI NIH HHS R01 CA222571NCI NIH HHS R01CA222571NIAMS NIH HHS R01 AR070877NIDCR NIH HHS R01 DE025866
6 · The paper itself

Abstract

Mechanical forces are fundamental regulators of cell behaviors. However, molecular regulation of mechanotransduction remain poorly understood. Here, we identified the mechanosensitive channels Piezo1 and Piezo2 as key force sensors required for bone development and osteoblast differentiation. Loss of Piezo1, or more severely Piezo1/2, in mesenchymal or osteoblast progenitor cells, led to multiple spontaneous bone fractures in newborn mice due to inhibition of osteoblast differentiation and increased bone resorption. In addition, loss of Piezo1/2 rendered resistant to further bone loss caused by unloading in both bone development and homeostasis. Mechanistically, Piezo1/2 relayed fluid shear stress and extracellular matrix stiffness signals to activate Ca

Indexed as

Adaptor Proteins, Signal TransducingAnimalsbeta CateninBone DevelopmentBone Marrow CellsCell Cycle ProteinsExtremitiesGene Expression Regulation, DevelopmentalIon ChannelsMechanotransduction, CellularMiceMice, KnockoutNFATC Transcription FactorsStromal CellsTissue Culture TechniquesYAP-Signaling ProteinsAdaptor Proteins, Signal Transducingbeta CateninCell Cycle ProteinsIon ChannelsNFATC Transcription FactorsPiezo1 protein, mousePiezo2 protein, mouseYap1 protein, mouseYAP-Signaling Proteinsbonedevelopmental biologyhippo signalingmechanotransductionmouseosteoblastpiezo1/2wnt signaling

Identifiers

PMID32186512
PMCPMC7112954
OpenAlexW3012397626

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.