Evidence map›Paper›PMID 31986145›Full record

ArticlePLoS computational biology2020

Notch signaling and taxis mechanisms regulate early stage angiogenesis: A mathematical and computational model.

Rocío Vega, Manuel Carretero, Rui D M Travasso, Luis L Bonilla

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

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  6. Wound healing and signaling pathways.Open life sciences · 2025
    Review
  7. YAP/TAZ drives Notch and angiogenesis mechanoregulation in silico.NPJ systems biology and applications · 2024
    Article
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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 3 institutions in 3 countries.

Rocío VegaG. Millán Institute for Fluid Dynamics, Nanoscience & Industrial Mathematics, and Department of Materials Science & Engineering and Chemical Engineering, Universidad Carlos III de Madrid, Leganés, Spain.ORCID 0000-0002-1878-6721
Manuel CarreteroG. Millán Institute for Fluid Dynamics, Nanoscience & Industrial Mathematics, and Department of Materials Science & Engineering and Chemical Engineering, Universidad Carlos III de Madrid, Leganés, Spain.ORCID 0000-0002-3517-4241
Rui D M TravassoCFisUC, Department of Physics, University of Coimbra, Coimbra, Portugal.ORCID 0000-0001-6078-0721
Luis L BonillaG. Millán Institute for Fluid Dynamics, Nanoscience & Industrial Mathematics, and Department of Materials Science & Engineering and Chemical Engineering, Universidad Carlos III de Madrid, Leganés, Spain.ORCID 0000-0002-7687-8595
Universidad Carlos III de Madrid · ESCourant Institute of Mathematical Sciences · USUniversity of Coimbra · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During angiogenesis, new blood vessels sprout and grow from existing ones. This process plays a crucial role in organ development and repair, in wound healing and in numerous pathological processes such as cancer progression or diabetes. Here, we present a mathematical model of early stage angiogenesis that permits exploration of the relative importance of mechanical, chemical and cellular cues. Endothelial cells proliferate and move over an extracellular matrix by following external gradients of Vessel Endothelial Growth Factor, adhesion and stiffness, which are incorporated to a Cellular Potts model with a finite element description of elasticity. The dynamics of Notch signaling involving Delta-4 and Jagged-1 ligands determines tip cell selection and vessel branching. Through their production rates, competing Jagged-Notch and Delta-Notch dynamics determine the influence of lateral inhibition and lateral induction on the selection of cellular phenotypes, branching of blood vessels, anastomosis (fusion of blood vessels) and angiogenesis velocity. Anastomosis may be favored or impeded depending on the mechanical configuration of strain vectors in the ECM near tip cells. Numerical simulations demonstrate that increasing Jagged production results in pathological vasculatures with thinner and more abundant vessels, which can be compensated by augmenting the production of Delta ligands.

Indexed as

Models, BiologicalAlgorithmsAnimalsComputational BiologyComputer SimulationNeovascularization, PathologicNeovascularization, PhysiologicReceptors, NotchSignal TransductionTaxis ResponseReceptors, Notch

Identifiers

PMID31986145
PMCPMC7021322
OpenAlexW3002923559

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.