Evidence map›Paper›PMID 34304293›Full record

ArticleEuropean biophysics journal : EBJ2022

Microfabricated cantilevers for parallelized cell-cell adhesion measurements.

Michele Zanetti, Suet Nee Chen, Martina Conti, Matthew R G Taylor, Orfeo Sbaizero, Luisa Mestroni, Marco Lazzarino

Abstract read
PubMed Publisher
In one paragraph

Article in European biophysics journal : EBJ, 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
0.3field-weighted citation impact, top 46% 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, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Nanoengineering for Mechanobiology "N4M-20".European biophysics journal : EBJ · 2022
    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

7 authors at 3 institutions in 2 countries.

Michele ZanettiCNR-IOM, Istituto Officina dei Materiali - Consiglio Nazionale delle Ricerche, 34149, Trieste, Italy.
Suet Nee ChenMolecular Genetics, Cardiovascular Institute, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, 80045-2507, USA.
Martina ContiCNR-IOM, Istituto Officina dei Materiali - Consiglio Nazionale delle Ricerche, 34149, Trieste, Italy.
Matthew R G TaylorMolecular Genetics, Cardiovascular Institute, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, 80045-2507, USA.
Orfeo SbaizeroUniversity of Trieste, 34127, Trieste, Italy.
Luisa MestroniMolecular Genetics, Cardiovascular Institute, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, 80045-2507, USA.
Marco LazzarinoCNR-IOM, Istituto Officina dei Materiali - Consiglio Nazionale delle Ricerche, 34149, Trieste, Italy. lazzarino@iom.cnr.it.ORCID http://orcid.org/0000-0003-1077-6569
University of Colorado Anschutz Medical Campus · USUniversity of Trieste · ITIstituto Officina dei Materiali · IT

Funding

Cardiomyocyte phenotype and mechanotransduction in Filamin C gene variants causing arrhythmogenic cardiomyopathyR01HL147064 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MESTRONI, LUISA, TAYLOR, MATTHEW R · 2020 to 2023
$2.1M
NHLBI NIH HHS R01 HL147064NIH HHS R01HL147064
6 · The paper itself

Abstract

Single-cell adhesion measured with atomic force microscopy (AFM) offers outstanding time and force resolution and allows the investigation of many important phenomena with unmatched precision. However, this technique suffers from serious practical limitations that hinder its effective application to a broader set of situations. Here we propose a different strategy based on the fabrication of large cantilevers and on the culture of the cells directly on them. Cantilevers are fabricated by standard micromachining, with an active area of 300 × 300 µm. A wedged structure is created so that the cantilever surface lies parallel to the substrate when mounted on an AFM system, so that the adhesion measurement probes the whole surface area at the same time. Thanks to the large area, cells can be seeded and grown on the cantilevers the day before the experiment, and let recover to optimal condition for the experiment. We used Human Embryonic Kidney cells, HEK 293A, to demonstrate the measurement of adhesion forces of up to 100 cells in parallel, and obtain a straightforward measurement of the average single cell adhesion energy. Our approach can improve significantly the cell-cell and cell-substrate adhesion statistics, reduce the experiment time and allow the investigation of the adhesion properties of cells that do not grow well in solution or on low adherent substrates, or that develop their characteristic features only after several hours or days of culture on a solid and adherent substrate.

Indexed as

Mechanical PhenomenaMicrotechnologyCell AdhesionHumansMicroscopy, Atomic Force

Identifiers

PMID34304293
OpenAlexW3186849777

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.