Evidence map›Paper›PMID 21435467›Full record

ArticleThe American journal of pathology2011

VAP-1-mediated M2 macrophage infiltration underlies IL-1β- but not VEGF-A-induced lymph- and angiogenesis.

Shintaro Nakao, Kousuke Noda, Souska Zandi, Dawei Sun, Mahdi Taher, Alexander Schering, Fang Xie, Yukihiko Mashima, Ali Hafezi-Moghadam

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
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  14. Cathepsin B-mediated CD18 shedding regulates leukocyte recruitment from angiogenic vessels.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  15. Article
  16. Review
  17. Phenotypic transformation of intimal and adventitial lymphatics in atherosclerosis: a regulatory role for soluble VEGF receptor 2.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Article
  18. Article
  19. Article
  20. Vascular adhesion protein 1 in the eye.Journal of ophthalmology · 2013
    Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Shintaro NakaoAngiogenesis Laboratory, Massachusetts Eye & Ear Infirmary, Boston, MA 02115, USA.
Kousuke Noda
Souska Zandi
Dawei Sun
Mahdi Taher
Alexander Schering
Fang Xie
Yukihiko Mashima
Ali Hafezi-Moghadam
Brigham and Women's Hospital · USMassachusetts Eye and Ear Infirmary · USUeno Gakuen University · JP

Funding

Mechanisms of Selectin Shedding in Leukocyte RecruitmentK08AI050775 · NIAID · MASSACHUSETTS EYE AND EAR INFIRMARY · PI HAFEZI-MOGHADAM, ALI · 2002 to 2004
$377k
NIAID NIH HHS K08 AI050775
6 · The paper itself

Abstract

Vascular adhesion protein-1 (VAP-1) contributes to inflammatory and angiogenic diseases, including cancer and age-related macular degeneration. It is expressed in blood vessels and contributes to inflammatory leukocyte recruitment. The cytokines IL-1β and vascular endothelial growth factor A (VEGF-A) modulate angiogenesis, lymphangiogenesis, and leukocyte infiltration. The lymphatic endothelium expresses intercellular adhesion molecule-1 and vascular adhesion molecule-1, which facilitate leukocyte transmigration into the lymphatic vessels. However, whether lymphatics express VAP-1 and whether they contribute to cytokine-dependent lymph- and angiogenesis are unknown. We investigated the role of VAP-1 in IL-1β- and VEGF-A-induced lymph- and angiogenesis using the established corneal micropocket assay. IL-1β increased VAP-1 expression in the inflamed cornea. Our in vivo molecular imaging revealed significantly higher VAP-1 expression in neovasculature than in the preexisting vessels. VAP-1 was expressed in blood but not lymphatic vessels in vivo. IL-1β-induced M2 macrophage infiltration and lymph- and angiogenesis were blocked by VAP-1 inhibition. In contrast, VEGF-A-induced lymph- and angiogenesis were unaffected by VAP-1 inhibition. Our results indicate a key role for VAP-1 in lymph- and angiogenesis-related macrophage recruitment. VAP-1 might become a new target for treatment of inflammatory lymph- and angiogenic diseases, including cancer.

Indexed as

LymphangiogenesisNeovascularization, PathologicAmine Oxidase (Copper-Containing)AnimalsCell Adhesion MoleculesCells, CulturedCorneaCytokinesHumansInterleukin-1betaMacrophagesMaleMiceMice, Inbred BALB CMicroscopy, FluorescenceVascular Endothelial Growth Factor AAmine Oxidase (Copper-Containing)Cell Adhesion MoleculesCytokinesInterleukin-1betasemicarbazide-sensitive amine oxidase-vascular adhesion protein-1, mouseVascular Endothelial Growth Factor A

Identifiers

PMID21435467
PMCPMC3078434
OpenAlexW2151803892

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.