Evidence map›Paper›PMID 24415663›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2014

Distribution of slow-cycling cells in epiphyseal cartilage and requirement of β-catenin signaling for their maintenance in growth plate.

Maria Elena Candela, Leslie Cantley, Rika Yasuaha, Masahiro Iwamoto, Maurizio Pacifici, Motomi Enomoto-Iwamoto

Open access · bronzeAbstract read
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Premature Growth Plate Closure Caused by a Hedgehog Cancer Drug Is Preventable by Co-Administration of a Retinoid Antagonist in Mice.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Article
  9. Review
  10. Review
  11. Niches for Skeletal Stem Cells of Mesenchymal Origin.Frontiers in cell and developmental biology · 2020
    Review
  12. Possible Contribution of Wnt-Responsive Chondroprogenitors to the Postnatal Murine Growth Plate.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    Article
  13. Intervertebral Disc Degeneration in a Percutaneous Mouse Tail Injury Model.American journal of physical medicine & rehabilitation · 2018
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Wnt signaling in cartilage development and diseases: lessons from animal studies.Laboratory investigation; a journal of technical methods and pathology · 2016
    Review
  20. 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

6 authors at 2 institutions in 2 countries.

Maria Elena CandelaTranslational Research Program in Pediatric Orthopaedics, Division of Orthopaedic Surgery, Department of Surgery, Children's Hospital of Philadelphia, 3615 Civic Center Boulevard, ARC 902, Philadelphia, Pennsylvania, 19104.
Leslie Cantley
Rika Yasuaha
Masahiro Iwamoto
Maurizio Pacifici
Motomi Enomoto-Iwamoto
Children's Hospital of Philadelphia · USShowa University · JP

Funding

Pathogenic Mechanisms in Hereditary Multiple Exostoses SyndromeR01AR061758 · NIAMS · CHILDREN'S HOSP OF PHILADELPHIA · PI Maurizio Pacifici · 2011 to 2026
$6.3M
TRANSCRIPTION FACTOR ERG AND SKELETOGENESISR01AR046000 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI IWAMOTO, MASAHIRO, PACIFICI, MAURIZIO · 1999 to 2016
$4.8M
Mechanisms of Synovial Joint FormationR01AR062908 · NIAMS · CHILDREN'S HOSP OF PHILADELPHIA · PI ENOMOTO-IWAMOTO, MOTOMI, PACIFICI, MAURIZIO · 2011 to 2020
$4.5M
NIAMS NIH HHS AR046000NIAMS NIH HHS AR061758NIAMS NIH HHS AR062908NIAMS NIH HHS R01 AR046000NIAMS NIH HHS R01 AR061758NIAMS NIH HHS R01 AR062908
6 · The paper itself

Abstract

Slow proliferation is one of the characteristics of stem cells. We examined the presence, distribution, and regulation of slow-cycling cells in the developing and growing skeleton using a pulse-chase method with a new nucleoside derivative, 5-ethynyl-2'-deoxyuridine (EdU). C57BL/6 mice received daily intraperitoneal injections of EdU from postnatal day 4 to day 7. One day after the last EdU injection, a large population of cells in articular cartilage and growth plate was labeled. Six weeks after the last injection, the number of EdU-labeled cells dramatically decreased, but a small number of them were dominantly present in the articular surface, and the labeling index was significantly higher in the surface than that in the rest of articular cartilage. In the growth plate, most EdU-positive cells were found in the top layer that lies immediately below the secondary ossification center. Interestingly, postnatal conditional ablation of β-catenin in cartilage caused a complete loss of the EdU-labeled cells in growth plate that displayed disorganization and dysfunction. Together, our data demonstrate that slow-cycling cells do reside in specific locations and numbers in both articular cartilage and growth plate. The β-catenin signaling pathway appears to play a previously unsuspected role in maintenance of the slow-cycling cells.

Indexed as

Animalsbeta CateninCartilage, ArticularCell CycleCell ProliferationDeoxyuridineGrowth PlateMiceMice, Inbred C57BLSignal Transduction5-ethynyl-2'-deoxyuridinebeta CateninDeoxyuridinecartilageslow-cycling cellsstem/progenitor cellsWnt/β-catenin signaling

Identifiers

PMID24415663
PMCPMC4114074
OpenAlexW1562142251

What OpenQuestion holds

Textmetadata
LicenceTDM
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.