Evidence map›Paper›PMID 25715693›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2015

Mesenchymal condensation-dependent accumulation of collagen VI stabilizes organ-specific cell fates during embryonic tooth formation.

Tadanori Mammoto, Akiko Mammoto, Amanda Jiang, Elisabeth Jiang, Basma Hashmi, Donald E Ingber

Open access · bronzeAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Mechanical control in dental and jaw morphogenesis and remodeling.International journal of oral science · 2026
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  11. A Window into Mammalian Basement Membrane Development: Insights from thebioRxiv : the preprint server for biology · 2023
    Article
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  15. Role of the lysyl oxidase family in organ development (Review).Experimental and therapeutic medicine · 2020
    Review
  16. Review
  17. Article
  18. Review
  19. Physical control of tissue morphogenesis across scales.Current opinion in genetics & development · 2018
    Review
  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

6 authors at 2 institutions in 1 country.

Tadanori MammotoVascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Akiko MammotoVascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Amanda JiangVascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Elisabeth JiangVascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Basma HashmiVascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Donald E IngberVascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Boston Children's Hospital · USHarvard University · US

Funding

Micromechanical Determinants of Organ Design and Engineering (SysCODE 6 of 10)RL1DE019023 · NIDCR · BOSTON CHILDREN'S HOSPITAL · PI INGBER, DONALD E · 2007 to 2011
$2.9M
Biomimetic Inductive Scaffolds for Tooth Organ EngineeringR56DE022803 · NIDCR · BOSTON CHILDREN'S HOSPITAL · PI INGBER, DONALD E · 2014 to 2014
$439k
NCI NIH HHS BC074986NIDCR NIH HHS 1R56DE022803-01A1NIDCR NIH HHS R56 DE022803NIDCR NIH HHS RL1 DE019023NIDCR NIH HHS RL1DE019023
6 · The paper itself

Abstract

backgroundMechanical compression of cells during mesenchymal condensation triggers cells to undergo odontogenic differentiation during tooth organ formation in the embryo. However, the mechanism by which cell compaction is stabilized over time to ensure correct organ-specific cell fate switching remains unknown.

resultsHere, we show that mesenchymal cell compaction induces accumulation of collagen VI in the extracellular matrix (ECM), which physically stabilizes compressed mesenchymal cell shapes and ensures efficient organ-specific cell fate switching during tooth organ development. Mechanical induction of collagen VI deposition is mediated by signaling through the actin-p38MAPK-SP1 pathway, and the ECM scaffold is stabilized by lysyl oxidase in the condensing mesenchyme. Moreover, perturbation of synthesis or cross-linking of collagen VI alters the size of the condensation in vivo.

conclusionsThese findings suggest that the odontogenic differentiation process that is induced by cell compaction during mesenchymal condensation is stabilized and sustained through mechanically regulated production of collagen VI within the mesenchymal ECM.

Indexed as

AnimalsCell LineageCell ShapeCollagen Type VIExtracellular Matrix ProteinsGene Expression ProfilingGene Expression Regulation, DevelopmentalMAP Kinase Signaling SystemMesodermMiceMicroarray AnalysisMolarOdontogenesisOrgan Specificityp38 Mitogen-Activated Protein KinasesPaired Box Transcription FactorsCollagen Type VIExtracellular Matrix ProteinsLox protein, mousep38 Mitogen-Activated Protein KinasesPaired Box Transcription FactorsPax9 protein, mousePAX9 Transcription FactorPlicamycinProtein Kinase InhibitorsProtein-Lysine 6-OxidaseSp1 Transcription Factoractincell compactionextracellular matrixLOXmechanicalmesenchymal condensationorganogenesisp38MAPKSP1tooth development

Identifiers

PMID25715693
PMCPMC4449280
OpenAlexW1512612434

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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.