Evidence map›Paper›PMID 39389439›Full record

ArticleBone2025

Piezo1 expression in mature osteocytes is dispensable for the skeletal response to mechanical loading.

Xuehua Li, Connie Zhang, Cameron E Vail, John T Sherrill, Jinhu Xiong

Abstract read
In one paragraph

Article in Bone, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Osteocalcin and GPR158: linking bone and brain function.Frontiers in cell and developmental biology · 2025
    Review
  10. Review
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

5 authors.

Xuehua LiDepartment of Orthopaedic Surgery, University of Arkansas for Medical Sciences, Little Rock, AR, USA; Center for Musculoskeletal Disease Research, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Connie ZhangDepartment of Orthopaedic Surgery, University of Arkansas for Medical Sciences, Little Rock, AR, USA; Center for Musculoskeletal Disease Research, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Cameron E VailDepartment of Orthopaedic Surgery, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
John T SherrillDepartment of Orthopaedic Surgery, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Jinhu XiongDepartment of Orthopaedic Surgery, University of Arkansas for Medical Sciences, Little Rock, AR, USA; Center for Musculoskeletal Disease Research, University of Arkansas for Medical Sciences, Little Rock, AR, USA. Electronic address: jxiong@uams.edu.

Funding

Understanding the Negative Prognostic Impact of Intraosseous Focal Lesions in Multiple MyelomaP20GM125503 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI CHARLES A O'BRIEN · 2018 to 2026
$23.0M
The role of Piezo1 in bone homeostasis and mechanotransductionR01AR076979 · NIAMS · UNIV OF ARKANSAS FOR MED SCIS · PI Jinhu Xiong · 2020 to 2026
$2.1M
NIAMS NIH HHS R01 AR076979NIGMS NIH HHS P20 GM125503
6 · The paper itself

Abstract

Mechanical loading is essential for bone growth and homeostasis, with osteocytes considered the primary mechanosensors. Deleting the mechanosensitive ion channel Piezo1 from Dmp1-Cre-targeted cells, which include both osteoblasts and osteocytes, resulted in reduced bone mass and impaired skeletal responses to mechanical stimuli. To specifically isolate Piezo1's role in osteocytes, we used Sost-Cre mice to generate mice with Piezo1 deletion exclusively in mature osteocytes. These mice exhibited lower bone mineral density, decreased cancellous bone mass, and reduced cortical thickness with decrease periosteal expansion. However, unlike mice lacking Piezo1 in both osteoblasts and osteocytes, those with Piezo1 deletion in mature osteocytes responded normally to mechanical loading. These findings suggest that Piezo1 expression in mature osteocytes contributes to bone maintenance under normal physiological condition, but is dispensable for the skeletal response to mechanical loading.

Indexed as

Ion ChannelsOsteocytesWeight-BearingAnimalsBone and BonesBone DensityGene DeletionMiceStress, MechanicalIon ChannelsPiezo1 protein, mouse

Identifiers

PMID39389439
PMCPMC11611638

What OpenQuestion holds

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Registered trials

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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.