Evidence map›Paper›PMID 24072879›Full record

ArticleJournal of leukocyte biology2014

TNF-α and IFN-γ promote lymphocyte adhesion to endothelial junctional regions facilitating transendothelial migration.

Justyna Jaczewska, Midhat H Abdulreda, Chi Y Yau, Martin M Schmitt, Irene Schubert, Per-Olof Berggren, Christian Weber, Rory R Koenen, Vincent T Moy, Ewa P Wojcikiewicz

Open access · bronzeAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. The Roles of Junctional Adhesion Molecules (JAMs) in Cell Migration.Frontiers in cell and developmental biology · 2022
    Review
  10. Review
  11. Review
  12. Review
  13. CRISPR-Based Activation of Endogenous Expression ofFrontiers in cell and developmental biology · 2021
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

10 authors at 3 institutions in 3 countries.

Justyna Jaczewska1.Florida Atlantic University, 777 Glades Rd., P.O. Box 3091, Boca Raton, FL 33431, USA. ewojciki@fau.edu.
Midhat H Abdulreda
Chi Y Yau
Martin M Schmitt
Irene Schubert
Per-Olof Berggren
Christian Weber
Rory R Koenen
Vincent T Moy
Ewa P Wojcikiewicz
University of Miami · USFlorida Atlantic University · USMaastricht University · NL

Funding

Protein-mediated molecular adhesion: AFM studiesR01GM055611 · NIGMS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MOY, VINCENT T · 2003 to 2006
$932k
Role of macrophages in pancreatic islet graft rejectionK01DK097194 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ABDULREDA, MIDHAT H · 2013 to 2015
$415k
PROTEIN MEDIATED MOLECULAR ADHESION--AFM STUDIESR29GM055611 · NIGMS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MOY, VINCENT T · 1997 to 2001
$315k
Noninvasive two-photon imaging of pancreatic islet graft rejection in the eyeF32DK083226 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ABDULREDA, MIDHAT H · 2009 to 2011
$151k
NIDDK NIH HHS F32 DK083226NIDDK NIH HHS F32DK083226NIDDK NIH HHS K01 DK097194NIGMS NIH HHS GM55611NIGMS NIH HHS R01 GM055611NIGMS NIH HHS R29 GM055611
6 · The paper itself

Abstract

Inflammatory conditions induce redistribution of junctional adhesion receptors toward the apical regions of endothelial cells promoting lymphocyte TEM. Much of the molecular structures of TEM have been revealed; however, the biophysical mechanisms underlying this process remain to be fully elucidated. Here, we used immunofluorescence microscopy and AFM to study endothelial distribution of adhesion molecules upon lymphocyte activation and transmigration. Our immunofluorescence results revealed redistribution of JAM-A and PECAM-1 but not ICAM-1 or VCAM-1 toward the apical junctional regions of HUVECs following a 6-h stimulation with TNF-α and IFN-γ. Consistently, our SCFS studies revealed that Jurkat cell adhesion to stimulated HUVEC monolayers was significantly greater in junctional regions. Enhanced adhesion was mediated mostly by JAM-A receptors. Further AFM adhesion mapping of the homophilic JAM-A/JAM-A interaction on the surfaces of HUVECs revealed a greater number of JAM-A receptors available for binding along junctional regions after TNF-α and IFN-γ stimulation. Our data reveal for the first time that adhesion "hot spots" of JAM-A receptors are involved in initiating lymphocyte TEM under inflammatory conditions.

Indexed as

Cell AdhesionCell Adhesion MoleculesCell CommunicationHumansHuman Umbilical Vein Endothelial CellsIntercellular JunctionsInterferon-gammaJurkat CellsLymphocytesMicroscopy, Atomic ForcePlatelet Endothelial Cell Adhesion Molecule-1Receptors, Cell SurfaceSpectrum AnalysisTransendothelial and Transepithelial MigrationTumor Necrosis Factor-alphaCell Adhesion MoleculesF11R protein, humanInterferon-gammaPlatelet Endothelial Cell Adhesion Molecule-1Receptors, Cell SurfaceTumor Necrosis Factor-alphaatomic force microscopyimmunofluorescence imagingjunctional adhesion molecule-Asingle-cell force spectroscopy

Identifiers

PMID24072879
PMCPMC3896659
OpenAlexW2153034056

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.