Evidence map›Paper›PMID 26133989›Full record

ArticlePloS one2015

The Role of Vascular Endothelial Growth Factor Receptor-1 Signaling in the Recovery from Ischemia.

Hideki Amano, Shintaro Kato, Yoshiya Ito, Koji Eshima, Fumihiro Ogawa, Ryo Takahashi, Kazuki Sekiguchi, Hideaki Tamaki, Hiroyuki Sakagami, Masabumi Shibuya and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. VEGFR1-tyrosine kinase signaling in pulmonary fibrosis.Inflammation and regeneration · 2021
    Review
  8. Review
  9. Article
  10. Skeletal muscle: A review of molecular structure and function, in health and disease.Wiley interdisciplinary reviews. Systems biology and medicine · 2020
    Review
  11. Article
  12. Article
  13. Imaging VEGF Receptors and αMolecular imaging and biology · 2018
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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 2 institutions in 1 country.

Hideki AmanoDepartments of Pharmacology, Kitasato University School of Medicine, Kanagawa, Japan.
Shintaro KatoDepartments of Pharmacology, Kitasato University School of Medicine, Kanagawa, Japan.
Yoshiya ItoDepartments of Surgery, Kitasato University School of Medicine, Kanagawa, Japan.
Koji EshimaDepartments of Immunology, Kitasato University School of Medicine, Kanagawa, Japan.
Fumihiro OgawaDepartments of Pharmacology, Kitasato University School of Medicine, Kanagawa, Japan.
Ryo TakahashiDepartments of Pharmacology, Kitasato University School of Medicine, Kanagawa, Japan.
Kazuki SekiguchiDepartments of Pharmacology, Kitasato University School of Medicine, Kanagawa, Japan.
Hideaki TamakiDepartments of Anatomy, Kitasato University School of Medicine, Kanagawa, Japan.
Hiroyuki SakagamiDepartments of Anatomy, Kitasato University School of Medicine, Kanagawa, Japan.
Masabumi ShibuyaGakubunkan Institute of Physiology and Medicine, Jobu University, Gunma, Japan.
Masataka MajimaDepartments of Pharmacology, Kitasato University School of Medicine, Kanagawa, Japan.
Kitasato University · JPJobu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular endothelial growth factor (VEGF) is one of the most potent angiogenesis stimulators. VEGF binds to VEGF receptor 1 (VEGFR1), inducing angiogenesis through the receptor's tyrosine kinase domain (TK), but the mechanism is not well understood. We investigated the role of VEGFR1 tyrosine kinase signaling in angiogenesis using the ischemic hind limb model. Relative to control mice, blood flow recovery was significantly impaired in mice treated with VEGFA-neutralizing antibody. VEGFR1 tyrosine kinase knockout mice (TK-/-) had delayed blood flow recovery from ischemia and impaired angiogenesis, and this phenotype was unaffected by treatment with a VEGFR2 inhibitor. Compared to wild type mice (WT), TK-/- mice had no change in the plasma level of VEGF, but the plasma levels of stromal-derived cell factor 1 (SDF-1) and stem cell factor, as well as the bone marrow (BM) level of pro-matrix metalloproteinase-9 (pro-MMP-9), were significantly reduced. The recruitment of cells expressing VEGFR1 and C-X-C chemokine receptor type 4 (CXCR4) into peripheral blood and ischemic muscles was also suppressed. Furthermore, WT transplanted with TK-/- BM significantly impaired blood flow recovery more than WT transplanted with WT BM. These results suggest that VEGFR1-TK signaling facilitates angiogenesis by recruiting CXCR4+VEGFR1+ cells from BM.

Indexed as

Neovascularization, PhysiologicAnimalsAntibodies, NeutralizingBlood Flow VelocityBone MarrowBone Marrow TransplantationChemokine CXCL12Gene Expression RegulationHindlimbIschemiaMaleMatrix Metalloproteinase 9MiceMice, Inbred C57BLMice, KnockoutReceptors, CXCR4Antibodies, NeutralizingChemokine CXCL12Cxcl12 protein, mouseCXCR4 protein, mouseMatrix Metalloproteinase 9Receptors, CXCR4Stem Cell FactorVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouseVascular Endothelial Growth Factor Receptor-1Vascular Endothelial Growth Factor Receptor-2

Identifiers

PMID26133989
PMCPMC4489890
OpenAlexW1846755436

What OpenQuestion holds

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LicenceCC BY
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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.