Evidence map›Paper›PMID 24764078›Full record

ArticleDevelopment (Cambridge, England)2014

A dynamic cell adhesion surface regulates tissue architecture in growth plate cartilage.

Sarah M Romereim, Nicholas H Conoan, Baojiang Chen, Andrew T Dudley

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Making and shaping endochondral and intramembranous bones.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Review
  11. Frontiers in genetics · 2021
    Article
  12. Endochondral growth zone pattern and activity in the zebrafish pharyngeal skeleton.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Article
  13. Article
  14. Review
  15. Article
  16. Non-pathological Chondrogenic Features of Valve Interstitial Cells in Normal Adult Zebrafish.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2019
    Article
  17. Article
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Sarah M RomereimDepartment of Genetics, Cell Biology, and Anatomy and the Mary and Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, 985965 Nebraska Medical Center, Omaha, NE 68198-5965, USA.
Nicholas H Conoan
Baojiang Chen
Andrew T Dudley
University of Nebraska Medical Center · USNorthwestern University · US

Funding

CELLULAR &MOLECULAR BASIS OF DISEASE TRAINING PROGRAMT32GM008061 · NIGMS · NORTHWESTERN UNIVERSITY · PI CARTHEW, RICHARD W. · 1985 to 2022
$17.1M
Regulation of Chondrocyte Morphogenesis by Wnt SignalingR01AR054857 · NIAMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DUDLEY, ANDREW T · 2008 to 2012
$1.4M
Live Growth Plate Cartilage Imaging to Study Proliferative Column FormationF31DE022511 · NIDCR · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ROMEREIM, SARAH M. · 2011 to 2014
$76k
NIAMS NIH HHS R01 AR054857NIDCR NIH HHS F31 DE022511NIGMS NIH HHS T32 GM008061NIGMS NIH HHS T32 GM08061
6 · The paper itself

Abstract

The architecture and morphogenetic properties of tissues are founded in the tissue-specific regulation of cell behaviors. In endochondral bones, the growth plate cartilage promotes bone elongation via regulated chondrocyte maturation within an ordered, three-dimensional cell array. A key event in the process that generates this cell array is the transformation of disordered resting chondrocytes into clonal columns of discoid proliferative cells aligned with the primary growth vector. Previous analysis showed that column-forming chondrocytes display planar cell divisions, and the resulting daughter cells rearrange by ∼90° to align with the lengthening column. However, these previous studies provided limited information about the mechanisms underlying this dynamic process. Here we present new mechanistic insights generated by application of a novel time-lapse confocal microscopy method along with immunofluorescence and electron microscopy. We show that, during cell division, daughter chondrocytes establish a cell-cell adhesion surface enriched in cadherins and β-catenin. Rearrangement into columns occurs concomitant with expansion of this adhesion surface in a process more similar to cell spreading than to migration. Column formation requires cell-cell adhesion, as reducing cadherin binding via chelation of extracellular calcium inhibits chondrocyte rearrangement. Importantly, physical indicators of cell polarity, such as cell body alignment, are not prerequisites for oriented cell behavior. Our results support a model in which regulation of adhesive surface dynamics and cortical tension by extrinsic signaling modifies the thermodynamic landscape to promote organization of daughter cells in the context of the three-dimensional growth plate tissue.

Indexed as

AnimalsAnimals, NewbornCartilageCell AdhesionCell DivisionCell MembraneCell PolarityCells, CulturedCell ShapeChondrocytesFemaleGrowth PlateMaleMiceMice, TransgenicAdhesionChondrogenesisMousePolarity

Identifiers

PMID24764078
PMCPMC4011088
OpenAlexW2162173421

What OpenQuestion holds

Textmetadata
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.