Evidence map›Paper›PMID 31790392›Full record

ArticlePLoS biology2019

Dynamic trafficking and turnover of JAM-C is essential for endothelial cell migration.

Katja B Kostelnik, Amy Barker, Christopher Schultz, Tom P Mitchell, Vinothini Rajeeve, Ian J White, Michel Aurrand-Lions, Sussan Nourshargh, Pedro Cutillas, Thomas D Nightingale

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Junctional adhesion molecule-C: A multifunctional mediator of cell adhesion.Cellular and molecular life sciences : CMLS · 2025
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. The Roles of Junctional Adhesion Molecules (JAMs) in Cell Migration.Frontiers in cell and developmental biology · 2022
    Review
  9. Use of Proximity Labeling in Cardiovascular Research.JACC. Basic to translational science · 2021
    Review
  10. Article
  11. Article
  12. Visualization of integrin molecules by fluorescence imaging and techniques.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2021
    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 2 countries.

Katja B KostelnikCentre for Microvascular Research, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, United Kingdom.
Amy BarkerCentre for Microvascular Research, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, United Kingdom.
Christopher SchultzCentre for Microvascular Research, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, United Kingdom.ORCID 0000-0001-5932-805X
Tom P MitchellCentre for Microvascular Research, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, United Kingdom.ORCID 0000-0003-2247-3098
Vinothini RajeeveCell Signalling & Proteomics Group, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Ian J WhiteMRC Laboratory of Molecular Cell Biology, University College London, London, United Kingdom.
Michel Aurrand-LionsAix Marseille University, CNRS, INSERM, Institut Paoli-Calmettes, CRCM, Marseille, France.ORCID 0000-0002-8361-3034
Sussan NoursharghCentre for Microvascular Research, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, United Kingdom.
Pedro CutillasCell Signalling & Proteomics Group, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.ORCID 0000-0002-3426-2274
Thomas D NightingaleCentre for Microvascular Research, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, United Kingdom.
Queen Mary University of London · GBCentre National de la Recherche Scientifique · FRMRC Laboratory for Molecular Cell Biology · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M006174/1Medical Research Council MC_U12266BMedical Research Council MR/M019179/1Wellcome TrustWellcome Trust 098291/Z/12/Z
6 · The paper itself

Abstract

Junctional complexes between endothelial cells form a dynamic barrier that hinders passive diffusion of blood constituents into interstitial tissues. Remodelling of junctions is an essential process during leukocyte trafficking, vascular permeability, and angiogenesis. However, for many junctional proteins, the mechanisms of junctional remodelling have yet to be determined. Here, we used receptor mutagenesis, horseradish peroxidase (HRP), and ascorbate peroxidase 2 (APEX-2) proximity labelling, alongside light and electron microscopy (EM), to map the intracellular trafficking routes of junctional adhesion molecule-C (JAM-C). We found that JAM-C cotraffics with receptors associated with changes in permeability such as vascular endothelial cadherin (VE-Cadherin) and neuropilin (NRP)-1 and 2, but not with junctional proteins associated with the transmigration of leukocytes. Dynamic JAM-C trafficking and degradation are necessary for junctional remodelling during cell migration and angiogenesis. By identifying new potential trafficking machinery, we show that a key point of regulation is the ubiquitylation of JAM-C by the E3 ligase Casitas B-lineage lymphoma (CBL), which controls the rate of trafficking versus lysosomal degradation.

Indexed as

Adaptor Proteins, Signal TransducingAntigens, CDCadherin 5CadherinsCapillary PermeabilityCell AdhesionCell Adhesion MoleculesCell MovementEndothelial CellsEndothelium, VascularHEK293 CellsHumansHuman Umbilical Vein Endothelial CellsIntercellular JunctionsJunctional Adhesion Molecule CLeukocytesAdaptor Proteins, Signal TransducingAntigens, CDCadherin 5CadherinsCBLB protein, humanCell Adhesion MoleculesJAM3 protein, humanJunctional Adhesion Molecule CNeuropilinsProto-Oncogene Proteins c-cbl

Identifiers

PMID31790392
PMCPMC6907879
OpenAlexW2989788087

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.