Evidence map›Paper›PMID 30484883›Full record

ArticleGlia2019

miR-30a-5p inhibition promotes interaction of Fas

Salome Murinello, Yoshihiko Usui, Susumu Sakimoto, Maki Kitano, Edith Aguilar, H Maura Friedlander, Amelia Schricker, Carli Wittgrove, Yoshihiro Wakabayashi, Michael I Dorrell and 2 more

Open access · greenAbstract read
In one paragraph

Article in Glia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  5. Mechanisms of action of retinal microglia in diabetic retinopathy (Review).International journal of molecular medicine · 2025
    Review
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  19. Review
  20. The innate immune system in diabetic retinopathy.Progress in retinal and eye research · 2021
    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

12 authors at 2 institutions in 2 countries.

Salome MurinelloDepartment of Molecular Medicine, The Scripps Research Institute, California.
Yoshihiko UsuiDepartment of Ophthalmology, Tokyo Medical University, Tokyo, Japan.
Susumu SakimotoDepartment of Molecular Medicine, The Scripps Research Institute, California.
Maki KitanoDepartment of Molecular Medicine, The Scripps Research Institute, California.
Edith AguilarDepartment of Molecular Medicine, The Scripps Research Institute, California.
H Maura FriedlanderDepartment of Molecular Medicine, The Scripps Research Institute, California.
Amelia SchrickerDepartment of Molecular Medicine, The Scripps Research Institute, California.
Carli WittgroveDepartment of Molecular Medicine, The Scripps Research Institute, California.
Yoshihiro WakabayashiDepartment of Ophthalmology, Tokyo Medical University, Tokyo, Japan.
Michael I DorrellDepartment of Molecular Medicine, The Scripps Research Institute, California.
Peter D WestenskowDepartment of Molecular Medicine, The Scripps Research Institute, California.
Martin FriedlanderDepartment of Molecular Medicine, The Scripps Research Institute, California.ORCID 0000-0003-4238-9651
Scripps Research Institute · USTokyo Medical University · JP

Funding

Adult Stem Cells for Therapy of Visual DisordersR24EY017540 · NEI · SCRIPPS RESEARCH INSTITUTE, THE · PI FRIEDLANDER, MARTIN · 2007 to 2011
$17.5M
INTEGRINS AND OCULAR ANGIOGENESISR01EY011254 · NEI · SCRIPPS RESEARCH INSTITUTE, THE · PI FRIEDLANDER, MARTIN · 1996 to 2016
$11.5M
MicroRNAs for therapy of visual disordersR24EY022025 · NEI · SCRIPPS RESEARCH INSTITUTE, THE · PI FRIEDLANDER, MARTIN · 2012 to 2016
$10.2M
NEI NIH HHS R01 EY011254NEI NIH HHS R24 EY017540NEI NIH HHS R24 EY022025NIH HHS EY022025NIH HHS EY11254NIH HHS R24
6 · The paper itself

Abstract

Ischemia-induced angiogenesis contributes to various neuronal and retinal diseases, and often results in neurodegeneration and visual impairment. Current treatments involve the use of anti-VEGF agents but are not successful in all cases. In this study we determined that miR-30a-5p is another important mediator of retinal angiogenesis. Using a rodent model of ischemic retinopathy, we show that inhibiting miR-30a-5p reduces neovascularization and promotes tissue repair, through modulation of microglial and endothelial cell cross-talk. miR-30a-5p inhibition results in increased expression of the death receptor Fas and CCL2, to decrease endothelial cell survival and promote microglial migration and phagocytic function in focal regions of ischemic injury. Our data suggest that miR-30a-5p inhibition accelerates tissue repair by enhancing FasL-Fas crosstalk between microglia and endothelial cells, to promote endothelial cell apoptosis and removal of dead endothelial cells. Finally, we found that miR-30a levels were increased in the vitreous of patients with proliferative diabetic retinopathy. Our study identifies a role for miR-30a in the pathogenesis of neovascular retinal disease by modulating microglial and endothelial cell function, and suggests it may be a therapeutic target to treat ischemia-mediated conditions.

Indexed as

AnimalsAnimals, NewbornApoptosisCell Line, TransformedCell ProliferationChemokine CCL2Disease Models, AnimalEndothelial Cellsfas ReceptorGene Expression RegulationHumansLectinsMiceMice, Inbred C57BLMice, TransgenicMicrogliaCcl2 protein, mouseChemokine CCL2Fas protein, mousefas ReceptorLectinsMicroRNAsMIRN30a microRNA, mouseRNA, MessengerangiogenesisCCL2ischemiamicrogliamiR-30a-5p

Identifiers

PMID30484883
PMCPMC6349526
OpenAlexW2902057094

What OpenQuestion holds

Textmetadata
LicenceTDM
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.