Evidence map›Paper›PMID 35338481›Full record

ArticleJournal of cellular physiology2022

Post natal expression of Prx1 labels appendicular restricted progenitor cell populations of multiple tissues.

Beth C Bragdon, Andrew Bennie, Amanda Molinelli, Yu Liu, Louis C Gerstenfeld

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. PRX1-positive mesenchymal stem cells drive molar morphogenesis.International journal of oral science · 2024
    Article
  3. Article
  4. Article
  5. Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetrance.Genetics in medicine : official journal of the American College of Medical Genetics · 2023
    Article
  6. Article
  7. Article
  8. Review
  9. Article
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 at 1 institution in 1 country.

Beth C BragdonDepartment of Orthopaedic Surgery, Boston University School of Medicine, Boston, Massachusetts, USA.ORCID 0000-0002-3270-127X
Andrew BennieDepartment of Orthopaedic Surgery, Boston University School of Medicine, Boston, Massachusetts, USA.
Amanda MolinelliDepartment of Orthopaedic Surgery, Boston University School of Medicine, Boston, Massachusetts, USA.
Yu LiuDepartment of Orthopaedic Surgery, Boston University School of Medicine, Boston, Massachusetts, USA.
Louis C GerstenfeldDepartment of Orthopaedic Surgery, Boston University School of Medicine, Boston, Massachusetts, USA.ORCID 0000-0002-0477-1211
Boston University · US

Funding

Project-005UL1TR001430 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BAIR-MERRITT, MEGAN H, CENTER, DAVID M. · 2015 to 2024
$52.3M
Role of Angiogenesis in Distraction OsteogenesisR01AR056637 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GERSTENFELD, LOUIS CHARLES · 2011 to 2015
$1.8M
The Characterization of the Skeletogenic Stem Cells that Contribute to Post Natal Axial Skeletal Tissue RepairR00AR068582 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BRAGDON, BETH CHRISTIE · 2018 to 2020
$735k
The Characterization of the Skeletogenic Stem Cells that Contribute to Post Natal Axial Skeletal Tissue RepairK99AR068582 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BRAGDON, BETH CHRISTIE · 2016 to 2017
$180k
NCATS NIH HHS UL1 TR001430NIAMS NIH HHS K99 AR068582NIAMS NIH HHS R00 AR068582NIAMS NIH HHS R01 AR056637
6 · The paper itself

Abstract

Currently, there is no consensus whether there is a single or multiple postnatal stem cell population(s) that contribute to skeletal homeostasis and postnatal bone formation. A known population of cells that express Prx1 contributes to postnatal bone formation. Prx1 expression also connotes calvaria and appendicular tissues during embryonic development. A transgenic tamoxifen inducible Prx1 reporter mouse was used for lineage tracking, to characterize the postnatal contribution of Prx1 expressing cells in skeletal homeostasis and bone formation. Under homeostatic conditions Prx1 labeling gave rise to a transient yet rapid turnover cell population at the periosteal and endosteal surfaces, along muscle fibers, and within the medial layers of vessels both within the muscle and marrow compartments of the appendicular skeleton. Fracture and ectopic bone formation of both fore and hind limbs showed recruitment and expansion of Prx1-derived cells in newly formed bone tissues. Prx1 labeled cells were limited or absent at axial skeletal sites during both homeostasis and after induction of bone formation. Last, Prx1-derived cells differentiated into multiple cell lineages including vascular smooth muscle, adipose, cartilage, and bone cells. These results show that Prx1 expression retained its embryonic tissue specification and connotes a stem/progenitor cell populations of mesenchymal tissue progenitors.

Indexed as

CartilageStem CellsAnimalsCell DifferentiationCell LineageFemaleHomeodomain ProteinsMiceMice, TransgenicPregnancySkullHomeodomain ProteinsPrrx1 protein, mousebone formationfractureMSCPrx1skeletal stem cell

Identifiers

PMID35338481
PMCPMC9133217
OpenAlexW4220751248

What OpenQuestion holds

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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.