Evidence map›Paper›PMID 19580776›Full record

ArticleBiophysical journal2009

Cell adhesion molecule distribution relative to neutrophil surface topography assessed by TIRFM.

Sandrine A Hocdé, Ollivier Hyrien, Richard E Waugh

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Visualization of integrin molecules by fluorescence imaging and techniques.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2021
    Article
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  15. Article
  16. Nanotopographical modification: a regulator of cellular function through focal adhesions.Nanomedicine : nanotechnology, biology, and medicine · 2010
    Review
  17. Article
  18. Article
  19. Article
  20. 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 at 1 institution in 1 country.

Sandrine A HocdéDepartment of Biomedical Engineering, University of Rochester, Rochester, New York, USA.
Ollivier Hyrien
Richard E Waugh
University of Rochester · US

Funding

VASCULAR RELATIONS OF BLOOD CELLS AND PROTEINSP01HL018208 · NHLBI · UNIVERSITY OF ROCHESTER · PI WAUGH, RICHARD E · 1985 to 2014
$24.7M
Statistical Inference on Chemotherapy Effects from Flow Cytometry DataR01CA134839 · NCI · UNIVERSITY OF ROCHESTER · PI HYRIEN, OLLIVIER · 2008 to 2012
$1.2M
NCI NIH HHS R01 CA134839NCI NIH HHS R01-CA134839NHLBI NIH HHS P01 HL018208NHLBI NIH HHS P01-HL18208
6 · The paper itself

Abstract

The positioning of adhesion molecules relative to the microtopography of the cell surface has a significant influence on the molecule's availability to form adhesive contacts. Measurements of the ratio of fluorescence intensity per unit area in epi-fluorescence images versus total internal reflection fluorescence images provides a means to assess the relative accessibility for bond formation of different fluorescently labeled molecules in cells pressed against a flat substrate. Measurements of the four principal adhesion molecules on human neutrophils reveal that L-selectin has the highest ratio of total internal reflection fluorescence/epi intensity, and that P-selectin glycoprotein ligand-1 (PSGL-1) and the integrins alphaLbeta2 (LFA-1) and alphaMbeta2 (Mac-1) have ratios similar to each other but lower than for L-selectin. All of the ratios increased with increasing impingement, indicating an alteration of surface topography with increasing surface compression. These results are consistent with model predictions for molecules concentrated near the tips of microvilli in the case of L-selectin, and sequestered away from the microvillus tips in the case of LFA-1, Mac-1, and PSGL-1. The results confirm differences among adhesion molecules in their surface distribution and reveal how the availability of specific adhesion molecules is altered by mechanical compression of the surface in live cells.

Indexed as

Cell Adhesion MoleculesCells, CulturedFluorescenceHumansLasersL-SelectinLymphocyte Function-Associated Antigen-1Macrophage-1 AntigenMembrane GlycoproteinsMicroscopy, FluorescenceModels, BiologicalNeutrophilsPressureCell Adhesion MoleculesL-SelectinLymphocyte Function-Associated Antigen-1Macrophage-1 AntigenMembrane GlycoproteinsP-selectin ligand protein

Identifiers

PMID19580776
PMCPMC2711387
OpenAlexW2033251296

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.