Evidence map›Paper›PMID 33715101›Full record

ArticleBiomechanics and modeling in mechanobiology2021

Cellular mitosis predicts vessel stability in a mechanochemical model of sprouting angiogenesis.

Patrick A Link, Rebecca L Heise, Seth H Weinberg

Open access · greenAbstract read
In one paragraph

Article in Biomechanics and modeling in mechanobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. [Research progress of matrix stiffness in regulating endothelial cell sprouting].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2023
    Review
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

3 authors at 2 institutions in 1 country.

Patrick A LinkDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA, USA.
Rebecca L HeiseDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA, USA.
Seth H WeinbergDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH, USA. weinberg.147@osu.edu.ORCID http://orcid.org/0000-0003-1170-0419
Virginia Commonwealth University · USThe Ohio State University · US

Funding

Mechanochemical Signaling Dynamics in Epithelial-Mesenchymal TransitionR01GM122855 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI LEMMON, CHRISTOPHER ANDREW, WEINBERG, SETH HOWARD · 2018 to 2021
$1.2M
Division of Chemical, Bioengineering, Environmental, and Transport Systems GRFP 2016207025Division of Civil, Mechanical and Manufacturing Innovation CMMI-1351162NIGMS NIH HHS R01 GM122855NIGMS NIH HHS R01GM122855
6 · The paper itself

Abstract

Angiogenesis, the formation of new vessels, occurs in both developmental and pathological contexts. Prior research has investigated vessel formation to identify cellular phenotypes and dynamics associated with angiogenic disease. One major family of proteins involved in angiogenesis are the Rho GTPases, which govern function related to cellular elongation, migration, and proliferation. Using a mechanochemical model coupling Rho GTPase activity and cellular and intercellular mechanics, we investigate the role of cellular mitosis on sprouting angiogenesis. Mitosis-GTPase synchronization was not a strong predictor of GTPase and thus vessel signaling instability, whereas the location of mitotic events was predicted to alter GTPase cycling instabilities. Our model predicts that middle stalk cells undergoing mitosis introduce irregular dynamics in GTPase cycling and may provide a source of aberrant angiogenesis. We also find that cellular and junctional tension exhibit spatial heterogeneity through the vessel, and that tension feedback, specifically in stalk cells, tends to increase the maximum forces generated in the vessel.

Indexed as

MitosisModels, BiologicalNeovascularization, PhysiologicBiomechanical PhenomenaBlood VesselsFeedback, PhysiologicalGTP PhosphohydrolasesGTP PhosphohydrolasesAngiogenesisMechanochemical modelRho GTPasesSpring-dashpot system

Identifiers

PMID33715101
PMCPMC8274398
OpenAlexW3136705171

What Socratic holds

Textmetadata
LicenceTDM
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.