Evidence map›Paper›PMID 17003499›Full record

ArticleThe American journal of pathology2006

Recruitment of a prostaglandin E receptor subtype, EP3-expressing bone marrow cells is crucial in wound-induced angiogenesis.

Emi Kamoshita, Yasuhiro Ikeda, Mamoru Fujita, Hideki Amano, Atsuhiko Oikawa, Tastunori Suzuki, Yasuhumi Ogawa, Shohei Yamashina, Sadahiro Azuma, Shuh Narumiya and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
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  11. Gastroduodenal mucosal defense.Current gastroenterology reports · 2008
    Review
  12. Prostaglandin E(2) receptors in bone formation.International orthopaedics · 2007
    Review
  13. 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

12 authors at 5 institutions in 2 countries.

Emi KamoshitaDepartment of Pharmacology, Kitasato University School of Medicine, Kanagawa 228-8555, Japan.
Yasuhiro Ikeda
Mamoru Fujita
Hideki Amano
Atsuhiko Oikawa
Tastunori Suzuki
Yasuhumi Ogawa
Shohei Yamashina
Sadahiro Azuma
Shuh Narumiya
Nobuya Unno
Masataka Majima
Beijing Obstetrics and Gynecology Hospital · CNKitasato University · JPInstitute of Animal Sciences · CNKitasato University Medical Center · JPKyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

E-type prostaglandins have been reported to be proangiogenic in vivo. Thus, we examined prostaglandin receptor signaling relevant to wound-induced angiogenesis. Full-thickness skin wounds were created on the backs of mice, and angiogenesis in wound granulation tissues was estimated. Wound closure and re-epithelization in EP3 receptor knockout mice (EP3-/-) were significantly delayed compared with their wild-type (WT) mice, whereas those in EP1-/-, EP2-/-, and EP4-/- were not delayed. Wound-induced angiogenesis estimated with CD31 immunohistochemistry in EP3-/- mice was significantly inhibited compared with that in WT mice. Immunoreactive vascular endothelial growth factor (VEGF) in wound granulation tissues in EP3-/- mice was markedly less than that in WT mice. Wound closure in WT mice was delayed significantly by VEGF neutralizing antibody compared with control IgG. Wound-induced angiogenesis and wound closure were significantly suppressed in EP3-/- bone marrow transplantation mice compared with those in WT bone marrow transplantation mice. These were accompanied with the reductions in accumulation of VEGF-expressing cells in wound granulation tissues and in mobilization of VEGF receptor 1-expressing leukocytes in peripheral circulation. These results indicate that the recruitment of EP3-expressing cells to wound granulation tissues is critical for surgical wound healing and angiogenesis via up-regulation of VEGF.

Indexed as

Neovascularization, PhysiologicWound HealingAnimalsAntibodiesBone Marrow CellsBone Marrow TransplantationDermatologic Surgical ProceduresEndothelial Growth FactorsMiceMice, KnockoutPlatelet Endothelial Cell Adhesion Molecule-1Receptors, Prostaglandin EReceptors, Prostaglandin E, EP3 SubtypeSignal TransductionSkinAntibodiesEndothelial Growth FactorsPlatelet Endothelial Cell Adhesion Molecule-1Ptger3 protein, mouseReceptors, Prostaglandin EReceptors, Prostaglandin E, EP3 Subtype

Identifiers

PMID17003499
PMCPMC1780188
OpenAlexW2109776354

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.