Evidence map›Paper›PMID 32528960›Full record

ArticleFrontiers in cell and developmental biology2020

NRP2 as an Emerging Angiogenic Player; Promoting Endothelial Cell Adhesion and Migration by Regulating Recycling of α5 Integrin.

Abdullah A A Alghamdi, Christopher J Benwell, Samuel J Atkinson, Jordi Lambert, Robert T Johnson, Stephen D Robinson

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 51 citations in OpenAlex.

  1. A who's who of cell types in skeletal muscle.Communications biology · 2026
    Review
  2. Article
  3. Smoking-Induced STC2Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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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

6 authors at 3 institutions in 1 country.

Abdullah A A AlghamdiSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, United Kingdom.
Christopher J BenwellGut Microbes and Health, Quadram Institute Bioscience, Norwich Research Park, Norwich, United Kingdom.
Samuel J AtkinsonSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, United Kingdom.
Jordi LambertFaculty of Medicine and Health Sciences, University of East Anglia, Norwich Research Park, Norwich, United Kingdom.
Robert T JohnsonSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, United Kingdom.
Stephen D RobinsonSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, United Kingdom.
Norwich Research Park · GBUniversity of East Anglia · GBQuadram Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/F/000PR10355British Heart Foundation PG/17/46/32880
6 · The paper itself

Abstract

Angiogenesis relies on the ability of endothelial cells (ECs) to migrate over the extracellular matrix via integrin receptors to respond to an angiogenic stimulus. Of the two neuropilin (NRP) orthologs to be identified, both have been reported to be expressed on normal blood and lymphatic ECs, and to play roles in the formation of blood and lymphatic vascular networks during angiogenesis. Whilst the role of NRP1 and its interactions with integrins during angiogenesis has been widely studied, the role of NRP2 in ECs is poorly understood. Here we demonstrate that NRP2 promotes Rac-1 mediated EC adhesion and migration over fibronectin (FN) matrices in a mechanistically distinct fashion to NRP1, showing no dependence on β3 integrin (ITGB3) expression, or VEGF stimulation. Furthermore, we highlight evidence of a regulatory crosstalk between NRP2 and α5 integrin (ITGA5) in ECs, with NRP2 depletion eliciting an upregulation of ITGA5 expression and disruptions in ITGA5 cellular organization. Finally, we propose a mechanism whereby NRP2 promotes ITGA5 recycling in ECs; NRP2 depleted ECs were found to exhibit reduced levels of total ITGA5 subunit recycling compared to wild-type (WT) ECs. Our findings expose NRP2 as a novel angiogenic player by promoting ITGA5-mediated EC adhesion and migration on FN.

Indexed as

cell migrationendotheliumintegrinsNeuropilinsprotein trafficking

Identifiers

PMID32528960
PMCPMC7264094
OpenAlexW3028395891

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.