Evidence map›Paper›PMID 25865282›Full record

ArticleNature communications2015

Dynamic imaging of the growth plate cartilage reveals multiple contributors to skeletal morphogenesis.

Yuwei Li, Vikas Trivedi, Thai V Truong, David S Koos, Rusty Lansford, Cheng-Ming Chuong, David Warburton, Rex A Moats, Scott E Fraser

Abstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Article
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  8. Resolving morphogenesis into quantifiable cell behaviours.Development (Cambridge, England) · 2022
    Article
  9. Review
  10. Article
  11. 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
  12. Article
  13. Making and shaping endochondral and intramembranous bones.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Review
  14. Macropinocytosis-mediated membrane recycling drives neural crest migration by delivering F-actin to the lamellipodium.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. Article
  16. Review
  17. Review
  18. Article
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  20. 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
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

9 authors.

Yuwei LiDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Vikas TrivediDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Thai V TruongDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California 91125, USA.
David S KoosDepartment of Radiology, The Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California 90027, USA.
Rusty LansfordDepartment of Radiology, The Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California 90027, USA.
Cheng-Ming ChuongDepartment of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
David WarburtonDevelopmental Biology and Regenerative Medicine Program, Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California 90027, USA.
Rex A MoatsDepartment of Radiology, The Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California 90027, USA.
Scott E FraserDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California 91125, USA.

Funding

Size regulation of skin appendagesR01AR047364 · NIAMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Cheng-Ming Chuong · 2002 to 2026
$10.1M
Tissue Engineering of New Hair FormationR01AR060306 · NIAMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHUONG, CHENG-MING · 2010 to 2019
$4.6M
NIAMS NIH HHS R01 AR047364NIAMS NIH HHS R01 AR060306
6 · The paper itself

Abstract

The diverse morphology of vertebrate skeletal system is genetically controlled, yet the means by which cells shape the skeleton remains to be fully illuminated. Here we perform quantitative analyses of cell behaviours in the growth plate cartilage, the template for long bone formation, to gain insights into this process. Using a robust avian embryonic organ culture, we employ time-lapse two-photon laser scanning microscopy to observe proliferative cells' behaviours during cartilage growth, resulting in cellular trajectories with a spreading displacement mainly along the tissue elongation axis. We build a novel software toolkit of quantitative methods to segregate the contributions of various cellular processes to the cellular trajectories. We find that convergent-extension, mitotic cell division, and daughter cell rearrangement do not contribute significantly to the observed growth process; instead, extracellular matrix deposition and cell volume enlargement are the key contributors to embryonic cartilage elongation.

Indexed as

AnimalsCartilageCell DivisionCell MovementCell SizeChick EmbryoChondrocytesExtracellular MatrixFibroblastsGene ExpressionGenes, ReporterGenetic VectorsGreen Fluorescent ProteinsGrowth PlateMetacarpal BonesMicroscopy, ConfocalGreen Fluorescent Proteins

Identifiers

PMID25865282
PMCPMC4403347

What Socratic 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 Socratic graph.