Evidence map›Paper›PMID 35582810›Full record

ArticleJournal of the Royal Society, Interface2022

Elucidating the signal for contact guidance contained in aligned fibrils with a microstructural-mechanical model.

Lauren M Bersie-Larson, Victor K Lai, Rohit Y Dhume, Paolo P Provenzano, Victor H Barocas, Robert T Tranquillo

Open access · greenAbstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

6 authors at 2 institutions in 1 country.

Lauren M Bersie-LarsonDepartment of Biomedical Engineering, University of Minnesota - Twin Cities, Minneapolis, MN 55455, USA.ORCID 0000-0001-8478-7514
Victor K LaiDepartment of Chemical Engineering, University of Minnesota - Duluth, Duluth, MN, USA.
Rohit Y DhumeDepartment of Mechanical Engineering, University of Minnesota - Twin Cities, Minneapolis, MN 55455, USA.
Paolo P ProvenzanoDepartment of Biomedical Engineering, University of Minnesota - Twin Cities, Minneapolis, MN 55455, USA.
Victor H BarocasDepartment of Biomedical Engineering, University of Minnesota - Twin Cities, Minneapolis, MN 55455, USA.
Robert T TranquilloDepartment of Biomedical Engineering, University of Minnesota - Twin Cities, Minneapolis, MN 55455, USA.
University of Minnesota · USUniversity of Minnesota, Duluth · US

Funding

Project 2: Cell Migration in Mechanically Complex MicroenvironmentsU54CA210190 · NCI · UNIVERSITY OF MINNESOTA · PI LARGAESPADA, DAVID ANDREW, ODDE, DAVID J. · 2016 to 2020
$10.0M
NCI NIH HHS U54 CA210190
6 · The paper itself

Abstract

Despite its importance in physiological processes and tissue engineering, the mechanism underlying cell contact guidance in an aligned fibrillar network has defied elucidation due to multiple interdependent signals that such a network presents to cells, namely, anisotropy of adhesion, porosity and mechanical behaviour. A microstructural-mechanical model of fibril networks was used to assess the relative magnitudes of these competing signals in networks of varied alignment strength based on idealized cylindrical pseudopods projected into the aligned and orthogonal directions and computing the anisotropy of metrics chosen for adhesion, porosity and mechanical behaviour: cylinder-fibre contact area for adhesion, persistence length of pores for porosity and total force to displace fibres from the cylindrical volume as well as network stiffness experienced upon cylinder retraction for mechanical behaviour. The signals related to mechanical anisotropy are substantially higher than adhesion and porosity anisotropy, especially at stronger network alignments, although their signal to noise (S/N) values are substantially lower. The former finding is consistent with a recent report that fibroblasts can sense fibril alignment via anisotropy of network mechanical resistance, and the model reveals this can be due to either mechanical resistance to pseudopod protrusion or retraction given their signal and S/N values are similar.

Indexed as

Cell CommunicationTissue EngineeringAnisotropyFibroblastsPorosityaligned fibril networkscell–matrix interactioncontact guidance

Identifiers

PMID35582810
PMCPMC9114932
OpenAlexW4280609857

What OpenQuestion holds

Textmetadata
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.