Evidence map›Paper›PMID 41096725›Full record

ReviewInternational journal of molecular sciences2025

Growth Plate Skeletal Stem Cells and Their Actions Within the Stem Cell Niche.

Natalie Kiat-Amnuay Cheng, Shion Orikasa, Noriaki Ono

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Bridging skeletal stem cell diversity and human skeletal modeling.Journal of bone and mineral metabolism · 2026
    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

3 authors.

Natalie Kiat-Amnuay ChengDepartment of Diagnostic and Biomedical Sciences, School of Dentistry, The University of Texas Health Science Center at Houston (UTHealth Houston), Houston, TX 77054, USA.
Shion OrikasaDepartment of Diagnostic and Biomedical Sciences, School of Dentistry, The University of Texas Health Science Center at Houston (UTHealth Houston), Houston, TX 77054, USA.ORCID 0000-0002-4226-7358
Noriaki OnoDepartment of Diagnostic and Biomedical Sciences, School of Dentistry, The University of Texas Health Science Center at Houston (UTHealth Houston), Houston, TX 77054, USA.ORCID 0000-0002-3771-8230

Funding

Skeletal stem cell plasticity in craniofacial bone diseases.R35DE034348 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Noriaki Ono · 2024 to 2026
$3.1M
Craniofacial skeletal cell lineage plasticity for reconstituting stem cells and their nichesR01DE030630 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ONO, NORIAKI, ONO, WANIDA · 2021 to 2025
$2.2M
National Institute of Health / National Institute of Dental and Craniofacial Research R35DE034348NIDCR NIH HHS R01 DE030630NIDCR NIH HHS R35 DE034348
6 · The paper itself

Abstract

The growth plate is a specialized cartilage structure near the ends of long bones that orchestrates longitudinal bone growth during fetal and postnatal stages. Within this region reside a dynamic population of growth plate skeletal stem cells (gpSSCs), primarily located in the resting zone, which possess self-renewal and multilineage differentiation capacity. Recent advances in cell-lineage tracing, single-cell transcriptomics, and in vivo functional studies have revealed distinct subpopulations of gpSSCs, which are defined by markers such as parathyroid hormone-related protein (PTHrP), CD73, axis inhibition protein 2 (Axin2), forkhead box protein A2 (FoxA2), and apolipoprotein E (ApoE). These stem cells interact intricately with their niche, particularly after the formation of the secondary ossification center, through stage-specific regulatory mechanisms involving several key signaling pathways. This review summarizes the current understanding of gpSSC identity, behavior, and regulation, focusing on how these cells sustain growth plate function through adapting to biomechanical and molecular cues.

Indexed as

Bone DevelopmentGrowth PlateStem Cell NicheStem CellsAnimalsCell CommunicationCell DifferentiationCell LineageCell Self RenewalHumansMiceModels, AnimalOsteogenesisSignal TransductionSingle-Cell Gene Expression Analysisapolipoprotein E (ApoE)Axis inhibition protein 2 (Axin2)CD73epiphyseal stem cell nicheforkhead box protein A2 (FoxA2)growth plateparathyroid hormone-related protein (PTHrP)resting zone chondrocytesskeletal stem cells

Identifiers

PMID41096725
PMCPMC12525321

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.