Evidence map›Paper›PMID 23315162›Full record

ArticleBlood2013

NRP1 acts cell autonomously in endothelium to promote tip cell function during sprouting angiogenesis.

Alessandro Fantin, Joaquim M Vieira, Alice Plein, Laura Denti, Marcus Fruttiger, Jeffrey W Pollard, Christiana Ruhrberg

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

102 citing papers in PubMed, 173 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Development of the blood-brain barrier.Development (Cambridge, England) · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. DNA G-Quadruplex in NRP1 Promoter Facilitates SARS-CoV-2 Infection.International journal of molecular sciences · 2024
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Review

42 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 2 countries.

Alessandro FantinUCL Institute of Ophthalmology, University College London, London, United Kingdom.
Joaquim M Vieira
Alice Plein
Laura Denti
Marcus Fruttiger
Jeffrey W Pollard
Christiana Ruhrberg
University College London · GBAlbert Einstein College of Medicine · US

Funding

Tumor Progression and MetastasisP01CA100324 · NCI · YESHIVA UNIVERSITY · PI CONDEELIS, JOHN S · 2003 to 2018
$30.0M
Macrophages and Tumor AngiogenesisR01CA131270 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI POLLARD, JEFFREY W. · 2008 to 2012
$1.7M
British Heart Foundation FS/10/54/28680British Heart Foundation PG/10/86/28622Medical Research Council G0501711Medical Research Council G0601093Medical Research Council G1002033NCI NIH HHS P01 CA100324NCI NIH HHS R01 CA131270Wellcome Trust 095623Wellcome Trust 095623/Z/11/Z
6 · The paper itself

Abstract

Neuropilin (NRP) 1 is a receptor for the vascular endothelial growth factor (VEGF)-A and is essential for normal angiogenesis. Previous in vitro experiments identified NRP1 interactions with VEGF-A's main signaling receptor VEGFR2 within endothelial cells, but also between nonendothelial NRP1 and endothelial VEGFR2. Consistent with an endothelial role for NRP1 in angiogenesis, we found that VEGFR2 and NRP1 were coexpressed in endothelial tip and stalk cells in the developing brain. In addition, NRP1 was expressed on two cell types that interact with growing brain vessels-the neural progenitors that secrete VEGF-A to stimulate tip cell activity and the pro-angiogenic macrophages that promote tip cell anastomosis. Selective targeting of Nrp1 in each of these cell types demonstrated that neural progenitor- and macrophage-derived NRP1 were dispensable, whereas endothelial NRP1 was essential for normal brain vessel growth. NRP1 therefore promotes brain angiogenesis cell autonomously in endothelium, independently of heterotypic interactions with nonendothelial cells. Genetic mosaic analyses demonstrated a key role for NRP1 in endothelial tip rather than stalk cells during vessel sprouting. Thus, NRP1-expressing endothelial cells attained the tip cell position when competing with NRP1-negative endothelial cells in chimeric vessel sprouts. Taken together, these findings demonstrate that NRP1 promotes endothelial tip cell function during angiogenesis.

Indexed as

AnimalsBlood VesselsCell PolarityEmbryo, MammalianEndothelial CellsEndothelium, VascularFemaleMiceMice, TransgenicModels, BiologicalMorphogenesisNeovascularization, PhysiologicNeuropilin-1Organ SpecificityPregnancyNeuropilin-1

Identifiers

PMID23315162
PMCPMC3606070
OpenAlexW2101706901

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.