Evidence map›Paper›PMID 27301418›Full record

ArticleImmunology and cell biology2016

Plasmin and regulators of plasmin activity control the migratory capacity and adhesion of human T cells and dendritic cells by regulating cleavage of the chemokine CCL21.

Natalie Lorenz, Evert Jan Loef, Inken D Kelch, Daniel J Verdon, Moyra M Black, Martin J Middleditch, David R Greenwood, E Scott Graham, Anna Es Brooks, P Rod Dunbar and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Immunology and cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Leukocyte Trafficking in Lymphatic Vessels.Cold Spring Harbor perspectives in medicine · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Neuroserpin: structure, function, physiology and pathology.Cellular and molecular life sciences : CMLS · 2021
    Review
  16. Review
  17. Scavenging of soluble and immobilized CCL21 by ACKR4 regulates peripheral dendritic cell emigration.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  18. Review
  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

11 authors at 1 institution in 1 country.

Natalie LorenzSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.ORCID 0000-0002-5480-1714
Evert Jan LoefSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.
Inken D KelchSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.
Daniel J VerdonSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.
Moyra M BlackSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.
Martin J MiddleditchSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.
David R GreenwoodSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.
E Scott GrahamCentre for Brain Research, Rangahau Roro, Aotearoa, New Zealand.
Anna Es BrooksSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.
P Rod DunbarSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.
Nigel P BirchSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.
University of Auckland · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The homeostatic chemokine CCL21 has a pivotal role in lymphocyte homing and compartment localisation within the lymph node, and also affects adhesion between immune cells. The effects of CCL21 are modulated by its mode of presentation, with different cellular responses seen for surface-bound and soluble forms. Here we show that plasmin cleaves surface-bound CCL21 to release the C-terminal peptide responsible for CCL21 binding to glycosaminoglycans on the extracellular matrix and cell surfaces, thereby generating the soluble form. Loss of this anchoring peptide enabled the chemotactic activity of CCL21 and reduced cell tethering. Tissue plasminogen activator did not cleave CCL21 directly but enhanced CCL21 processing through generation of plasmin from plasminogen. The tissue plasminogen activator inhibitor neuroserpin prevented processing of CCL21 and blocked the effects of soluble CCL21 on cell migration. Similarly, the plasmin-specific inhibitor α

Indexed as

alpha-2-AntiplasminAmino Acid SequenceCell AdhesionCell CommunicationCell MembraneCell MovementChemokine CCL21Dendritic CellsHumansNeuropeptidesNeuroserpinPlasminogenProtein BindingRecombinant ProteinsSerpinsTissue Plasminogen Activatoralpha-2-AntiplasminCCL21 protein, humanChemokine CCL21NeuropeptidesNeuroserpinPlasminogenRecombinant ProteinsSerpinsTissue Plasminogen Activator

Identifiers

PMID27301418
OpenAlexW2432031225

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.