Evidence map›Paper›PMID 23071433›Full record

ArticlePLoS computational biology2012

MOSAIC: a multiscale model of osteogenesis and sprouting angiogenesis with lateral inhibition of endothelial cells.

Aurélie Carlier, Liesbet Geris, Katie Bentley, Geert Carmeliet, Peter Carmeliet, Hans Van Oosterwyck

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. AnFrontiers in bioengineering and biotechnology · 2023
    Article
  5. Review
  6. Review
  7. Article
  8. TowardsFrontiers in bioengineering and biotechnology · 2021
    Review
  9. Article
  10. Article
  11. The endothelial tip-stalk cell selection and shuffling during angiogenesis.Journal of cell communication and signaling · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. A review of computational models of bone fracture healing.Medical & biological engineering & computing · 2017
    Review
  18. Review
  19. Article
  20. Multiscale modeling methods in biomechanics.Wiley interdisciplinary reviews. Systems biology and medicine · 2017
    Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Aurélie CarlierBiomechanics Section, KU Leuven, Leuven, Belgium.
Liesbet Geris
Katie Bentley
Geert Carmeliet
Peter Carmeliet
Hans Van Oosterwyck
KU Leuven · BECancer Research UK · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The healing of a fracture depends largely on the development of a new blood vessel network (angiogenesis) in the callus. During angiogenesis tip cells lead the developing sprout in response to extracellular signals, amongst which vascular endothelial growth factor (VEGF) is critical. In order to ensure a correct development of the vasculature, the balance between stalk and tip cell phenotypes must be tightly controlled, which is primarily achieved by the Dll4-Notch1 signaling pathway. This study presents a novel multiscale model of osteogenesis and sprouting angiogenesis, incorporating lateral inhibition of endothelial cells (further denoted MOSAIC model) through Dll4-Notch1 signaling, and applies it to fracture healing. The MOSAIC model correctly predicted the bone regeneration process and recapitulated many experimentally observed aspects of tip cell selection: the salt and pepper pattern seen for cell fates, an increased tip cell density due to the loss of Dll4 and an excessive number of tip cells in high VEGF environments. When VEGF concentration was even further increased, the MOSAIC model predicted the absence of a vascular network and fracture healing, thereby leading to a non-union, which is a direct consequence of the mutual inhibition of neighboring cells through Dll4-Notch1 signaling. This result was not retrieved for a more phenomenological model that only considers extracellular signals for tip cell migration, which illustrates the importance of implementing the actual signaling pathway rather than phenomenological rules. Finally, the MOSAIC model demonstrated the importance of a proper criterion for tip cell selection and the need for experimental data to further explore this. In conclusion, this study demonstrates that the MOSAIC model creates enhanced capabilities for investigating the influence of molecular mechanisms on angiogenesis and its relation to bone formation in a more mechanistic way and across different time and spatial scales.

Indexed as

Models, BiologicalAnimalsBony CallusComputational BiologyComputer SimulationEndothelial CellsFracture HealingIntracellular Signaling Peptides and ProteinsMembrane ProteinsMiceNeovascularization, PhysiologicOsteogenesisRatsReceptor, Notch1Signal TransductionVascular Endothelial Growth Factor Receptor-2delta proteinIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptor, Notch1Vascular Endothelial Growth Factor Receptor-2

Identifiers

PMID23071433
PMCPMC3469420
OpenAlexW2043248205

What OpenQuestion 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 OpenQuestion graph.