Evidence map›Paper›PMID 21152375›Full record

ArticleJournal of physics. Condensed matter : an Institute of Physics journal2010

Detecting cell-adhesive sites in extracellular matrix using force spectroscopy mapping.

Somyot Chirasatitsin, Adam J Engler

Open access · greenAbstract read
In one paragraph

Article in Journal of physics. Condensed matter : an Institute of Physics journal, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Dynamic and reversible surface topography influences cell morphology.Journal of biomedical materials research. Part A · 2013
    Article
  8. Cell instructive microporous scaffolds through interface engineering.Journal of the American Chemical Society · 2012
    Article
  9. Article
  10. Wet nanoscale imaging and testing of polymersomes.Small (Weinheim an der Bergstrasse, Germany) · 2011
    Article
  11. 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

2 authors at 1 institution in 1 country.

Somyot ChirasatitsinDepartment of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA.
Adam J Engler
University of California, San Diego · US

Funding

"Smart" Materials to Engineer a More Complete Stem Cell NicheDP2OD006460 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ENGLER, ADAM J · 2009 to 2009
$2.3M
NIH HHS 1DP02OD10322765NIH HHS DP2 OD006460
6 · The paper itself

Abstract

The cell microenvironment is composed of extracellular matrix (ECM), which contains specific binding sites that allow the cell to adhere to its surroundings. Cells employ focal adhesion proteins, which must be able to resist a variety of forces to bind to ECM. Current techniques for detecting the spatial arrangement of these adhesions, however, have limited resolution and those that detect adhesive forces lack sufficient spatial characterization or resolution. Using a unique application of force spectroscopy, we demonstrate here the ability to determine local changes in the adhesive property of a fibronectin substrate down to the resolution of the fibronectin antibody-functionalized tip diameter, ~20 nm. To verify the detection capabilities of force spectroscopy mapping (FSM), changes in loading rate and temperature were used to alter the bond dynamics and change the adhesion force. Microcontact printing was also used to pattern fluorescein isothiocyanate-conjugated fibronectin in order to mimic the discontinuous adhesion domains of native ECM. Fluorescent detection was used to identify the pattern while FSM was used to map cell adhesion sites in registry with the initial fluorescent image. The results show that FSM can be used to detect the adhesion domains at high resolution and may subsequently be applied to native ECM with randomly distributed cell adhesion sites.

Indexed as

Cell AdhesionExtracellular MatrixExtracellular Matrix ProteinsFocal AdhesionsMicroscopy, Atomic ForceExtracellular Matrix Proteins

Identifiers

PMID21152375
PMCPMC2997741
OpenAlexW2071433147

What OpenQuestion holds

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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.