Evidence map›Paper›PMID 28447179›Full record

ArticleAnnals of biomedical engineering2017

Influence of Inherent Mechanophenotype on Competitive Cellular Adherence.

Manisha K Shah, Iris H Garcia-Pak, Eric M Darling

Open access · greenAbstract read
In one paragraph

Article in Annals of biomedical engineering, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Selection of Force Sensors forTissue engineering. Part A · 2025
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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

3 authors at 1 institution in 1 country.

Manisha K ShahCenter for Biomedical Engineering, Brown University, 175 Meeting Street, Box G-B397, Providence, RI, USA.
Iris H Garcia-PakCenter for Biomedical Engineering, Brown University, 175 Meeting Street, Box G-B397, Providence, RI, USA.
Eric M DarlingCenter for Biomedical Engineering, Brown University, 175 Meeting Street, Box G-B397, Providence, RI, USA. Eric_Darling@brown.edu.ORCID 0000-0002-3932-8623
Brown University · US

Funding

COBRE for Skeletal Health and RepairP20GM104937 · NIGMS · RHODE ISLAND HOSPITAL · PI CHEN, QIAN · 2012 to 2016
$10.8M
Pilot Projects ProgramP30GM122732 · NIGMS · RHODE ISLAND HOSPITAL · PI CHEN, QIAN · 2017 to 2021
$6.6M
High-yield, lineage-specific enrichment of living mesenchymal stem cellsR01AR063642 · NIAMS · BROWN UNIVERSITY · PI DARLING, ERIC M · 2013 to 2018
$1.8M
NIAMS NIH HHS R01 AR063642NIGMS NIH HHS P20 GM104937NIGMS NIH HHS P30 GM122732
6 · The paper itself

Abstract

Understanding the role of mechanophenotype in competitive adherence of cells to other cells versus underlying substrates can inform such processes as tissue development, cancer progression, and wound healing. This study investigated how mechanophenotype, defined by whole-cell, elastic/viscoelastic properties for the perinuclear region, and cellular assembly are intertwined through the mechanosensing process. Atomic force microscopy was used to characterize the temporal elastic/viscoelastic properties of individual and assembled fibroblasts grown on substrates with elastic moduli above, below, or similar to whole-cell mechanophenotypes measured for three, genetically modified cell lines. All cells were at their most compliant immediately after plating but transitioned to distinct, stiffer mechanophenotypes by Day 1 after acclimation. This mechanical state, and cellular assembly/morphology, did not change significantly over the following three days of testing, regardless of substrate compliance or cellular organization (multi-cell nodules/plaques or single cells). Interestingly, cells formed 3D nodules when attached to substrates with elastic moduli less than their own but spread readily on substrates with moduli equal to or greater than their own, suggesting a preference to adhere to the stiffest surface sensed (substrate or cell). This suggests that inherent mechanophenotype plays a role as a competing surface during microenvironment mechanosensing and subsequent cell-cell-substrate organization.

Indexed as

Models, BiologicalCell AdhesionCell Adhesion MoleculesCell CommunicationCell LineComputer SimulationElastic ModulusEquipment DesignEquipment Failure AnalysisExtracellular MatrixExtracellular Matrix ProteinsFibroblastsHumansMechanotransduction, CellularReproducibility of ResultsSensitivity and SpecificityCell Adhesion MoleculesExtracellular Matrix ProteinsAtomic force microscopyCellular assemblyElastic/viscoelastic propertiesMechanosensingNodulePlaque

Identifiers

PMID28447179
PMCPMC5529242
OpenAlexW2608262603

What OpenQuestion 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 OpenQuestion graph.