Evidence map›Paper›PMID 29301231›Full record

ArticleInternational journal of molecular sciences2017

Apolipoprotein M Inhibits Angiogenic and Inflammatory Response by Sphingosine 1-Phosphate on Retinal Pigment Epithelium Cells.

Ryo Terao, Megumi Honjo, Makoto Aihara

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. 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
2.2field-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

13 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. HDL Composition, Heart Failure, and Its Comorbidities.Frontiers in cardiovascular medicine · 2022
    Review
  7. Article
  8. Lipid Signaling in Ocular Neovascularization.International journal of molecular sciences · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. Sphingolipids as Emerging Mediators in Retina Degeneration.Frontiers in cellular neuroscience · 2019
    Review
  13. Targeting Lipid Metabolism for the Treatment of Age-Related Macular Degeneration: Insights from Preclinical Mouse Models.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics
    Review
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

3 authors at 1 institution in 1 country.

Ryo TeraoDepartment of Ophthalmology, Graduate School of Medicine, Tokyo University, Tokyo 113-8654, Japan. qqaf787c9@gmail.com.
Megumi HonjoDepartment of Ophthalmology, Graduate School of Medicine, Tokyo University, Tokyo 113-8654, Japan. m_honjo@kuhp.kyoto-u.ac.jp.
Makoto AiharaDepartment of Ophthalmology, Graduate School of Medicine, Tokyo University, Tokyo 113-8654, Japan. aihara-tky@umin.net.
The University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingosine 1-phosphate (S1P) is a potent lipid mediator that modulates inflammatory responses and proangiogenic factors. It has been suggested that S1P upregulates choroidal neovascularization (CNV) and may be deeply involved in the pathogenesis of exudative age-related macular degeneration (AMD). Recent studies have suggested that apolipoprotein M (ApoM), a carrier protein for S1P, modulates the biological properties of S1P in the pathogenesis of atherosclerosis. However, the role of ApoM/S1P in AMD has not been explored. We investigated the effect of S1P on proangiogenic factors in human retinal pigment epithelium (RPE) cell lines in vitro. S1P promoted the expression of vascular endothelial growth factor in RPE cells. Hypoxia inducible factor-1α expression was also upregulated. These S1P-induced enhancements in growth factors and chemotactic cytokines in RPE cells were significantly inhibited by ApoM treatment. Additionally, in vivo experiments using a laser-induced CNV murine model demonstrated that intravitreal ApoM injection significantly reduced the progression of CNV formation. Although the detailed mechanisms remain to be elucidated, the present results provide a novel potential therapeutic target for AMD, and demonstrate a suppressive role for ApoM and S1P in the pathology of CNV progression.

Indexed as

AnimalsApolipoproteins MCell LineChoroidal NeovascularizationCytokinesHumansInflammationIntercellular Signaling Peptides and ProteinsLasersLysophospholipidsMacular DegenerationMiceRetinaRetinal Pigment EpitheliumSphingosineApolipoproteins MCytokinesIntercellular Signaling Peptides and ProteinsLysophospholipidsSphingosinesphingosine 1-phosphateage-related macular degenerationapolipoprotein Mchoroidal neovascularizationhigh-density lipoproteinhypoxia inducible factorinterleukin-8S1P-receptorssphingolipids and inflammationsphingosine 1-phosphatevascular endothelial growth factor

Identifiers

PMID29301231
PMCPMC5796061
OpenAlexW2786545950

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.