Evidence map›Paper›PMID 41736692›Full record

ArticleStem cells translational medicine2026

FGF2 alters the calvarial suture niche homeostasis shifting skeletal stem cell/progenitors toward an osteo-angiogenic coupling fate.

Natalina Quarto, Siddharth Menon, Jason L Guo, Ankit Salhotra, Michael T Longaker

Abstract read
In one paragraph

Article in Stem cells translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Natalina QuartoHagey Laboratory for Pediatric Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, United States.ORCID 0000-0002-5473-7847
Siddharth MenonHagey Laboratory for Pediatric Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, United States.
Jason L GuoHagey Laboratory for Pediatric Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, United States.
Ankit SalhotraHagey Laboratory for Pediatric Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, United States.ORCID 0000-0001-6107-6656
Michael T LongakerHagey Laboratory for Pediatric Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, United States.

Funding

Center for Dental, Oral, and Craniofacial Tissue and Organ Regeneration (C-DOCTOR)U24DE029463 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHAI, YANG, LOTZ, JEFFREY C. · 2020 to 2024
$29.5M
Stanford Islet Research CoreP30DK116074 · NIDDK · STANFORD UNIVERSITY · PI Seung K Kim · 2017 to 2026
$19.5M
Identifying the human skeletal stem cell.R01DE027323 · NIDCR · STANFORD UNIVERSITY · PI LONGAKER, MICHAEL T · 2018 to 2022
$1.9M
Cellular and Mechanical Mechanisms Regulating Mandibular Distraction OsteogenesisR01DE026730 · NIDCR · STANFORD UNIVERSITY · PI LONGAKER, MICHAEL T · 2017 to 2021
$1.9M
NIDCR NIH HHS R01 DE026730NIDCR NIH HHS R01 DE027323NIDCR NIH HHS U24 DE029463NIDDK NIH HHS P30 DK116074NIH HHS R01DE026730NIH HHS R01DE027323NIH HHS U24DE029463
6 · The paper itself

Abstract

Calvarial sutures, the major growth centers for skull morphogenesis, are currently regarded as "niches" for calvarial stem cells. Our previous study has identified a skeletal stem/progenitor cell population resident within the suture mesenchyme. Moreover, we have shown that decrease and/or imbalance of their representation in the "niche" impact the fate of a non-fusing suture to fusing-suture and vice versa. Herein, taking advantage of an our established ex vivo calvarial suture explant model we investigated the impact triggered by FGF2, a pro-osteogenic and pro-angiogenic factor, on our skeletal stem/progenitor cell population resident in the suture mesenchyme. Multi-omics data integration combined with cell biology identifies dynamic changes in the representation of skeletal stem/progenitor cell population thus, unveiling within them functionally distinct populations with angiogenesis-competent properties. Findings altogether indicate that FGF2 stimuli may alter the suture "niche" homeostasis and that coordinate an osteogenesis-angiogenesis coupling within skeletal stem/progenitor cell sub-populations.

Indexed as

AngiogenesisCranial SuturesFibroblast Growth Factor 2HomeostasisNeovascularization, PhysiologicOsteogenesisSkullStem Cell NicheStem CellsAnimalsCell DifferentiationMiceFibroblast Growth Factor 2angiogenesiscalvarial-sutureFGF2nicheskeletal stem cell

Identifiers

PMID41736692
PMCPMC12932999

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.