Evidence map›Paper›PMID 23722647›Full record

ArticleJournal of biomechanical engineering2013

Complex matrix remodeling and durotaxis can emerge from simple rules for cell-matrix interaction in agent-based models.

James W Reinhardt, Daniel A Krakauer, Keith J Gooch

Abstract read
In one paragraph

Article in Journal of biomechanical engineering, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Mechanical Model for Durotactic Cell Migration.ACS biomaterials science & engineering · 2019
    Article
  7. Computational modeling of three-dimensional ECM-rigidity sensing to guide directed cell migration.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. A mathematical model of collagen lattice contraction.Journal of the Royal Society, Interface · 2014
    Article
  16. Multiscale mechanical simulations of cell compacted collagen gels.Journal of biomechanical engineering · 2013
    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

3 authors.

James W ReinhardtDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH 43210, USA.
Daniel A Krakauer
Keith J Gooch

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using a top-down approach, an agent-based model was developed within NetLogo where cells and extracellular matrix (ECM) fibers were composed of multiple agents to create deformable structures capable of exerting, reacting to, and transmitting mechanical force. At the beginning of the simulation, long fibers were randomly distributed and cross linked. Throughout the simulation, imposed rules allowed cells to exert traction forces by extending pseudopodia, binding to fibers and pulling them towards the cell. Simulated cells remodeled the fibrous matrix to change both the density and alignment of fibers and migrated within the matrix in ways that are consistent with previous experimental work. For example, cells compacted the matrix in their pericellular regions much more than the average compaction experienced for the entire matrix (696% versus 21%). Between pairs of cells, the matrix density increased (by 92%) and the fibers became more aligned (anisotropy index increased from 0.45 to 0.68) in the direction parallel to a line connecting the two cells, consistent with the "lines of tension" observed in experiments by others. Cells migrated towards one another at an average rate of ∼0.5 cell diameters per 10,000 arbitrary units (AU); faster migration occurred in simulations where the fiber density in the intercellular area was greater. To explore the potential contribution of matrix stiffness gradients in the observed migration (i.e., durotaxis), the model was altered to contain a regular lattice of fibers possessing a stiffness gradient and just a single cell. In these simulations cells migrated preferentially in the direction of increasing stiffness at a rate of ∼2 cell diameter per 10,000 AU. This work demonstrates that matrix remodeling and durotaxis, both complex phenomena, might be emergent behaviors based on just a few rules that control how a cell can interact with a fibrous ECM.

Indexed as

Models, BiologicalAnimalsCell MovementCell Physiological PhenomenaComputer SimulationElastic ModulusExtracellular MatrixHumansMechanotransduction, CellularStress, Mechanical

Identifiers

PMID23722647
PMCPMC3705834

What OpenQuestion holds

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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.