Evidence map›Paper›PMID 27611191›Full record

ArticlePloS one2016

Exogenous Modulation of Retinoic Acid Signaling Affects Adult RGC Survival in the Frog Visual System after Optic Nerve Injury.

Mildred V Duprey-Díaz, Jonathan M Blagburn, Rosa E Blanco

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. 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
0.8field-weighted citation impact, top 29% 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, 17 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. MAPK/ERK Pathway as a Central Regulator in Vertebrate Organ Regeneration.International journal of molecular sciences · 2022
    Review
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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 2 institutions in 1 country.

Mildred V Duprey-DíazDepartment of Anatomy and Neurobiology, School of Medicine, University of Puerto Rico, San Juan, PR, United States of America.
Jonathan M BlagburnInstitute of Neurobiology, University of Puerto Rico Medical Sciences Campus, San Juan, PR, United States of America.
Rosa E BlancoDepartment of Anatomy and Neurobiology, School of Medicine, University of Puerto Rico, San Juan, PR, United States of America.
University of Puerto Rico, Medical Sciences Campus · PRUniversity of Puerto Rico System · PR

Funding

RISE Option III: MBRS RISE at the UPR Medical Sciences CampusR25GM061838 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI CADILLA, CARMEN LYDIA · 2000 to 2021
$25.5M
The Role of Sensory Input to Mammalian Locomotion After the Loss of supraspinal.P20GM103642 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI LASALDE-DOMINICCI, JOSE ANTONIO · 2013 to 2023
$20.6M
TRANSLATIONAL PROTEOMICS CENTERG12MD007600 · NIMHD · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI FERNANDEZ-REPOLLET, EMMA · 2012 to 2016
$11.0M
Engrailed targets and the control of synaptic circuits in DrosophilaSC1NS081726 · NINDS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI BLAGBURN, JONATHAN M · 2012 to 2015
$1.5M
Effects of Retinoic Acid Signaling on Retinal Ganglion Cell Survival and RegenerationSC3GM116692 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI BLANCO, ROSA E. · 2016 to 2019
$450k
NIGMS NIH HHS P20 GM103642NIGMS NIH HHS R25 GM061838NIGMS NIH HHS SC3 GM116692NIMHD NIH HHS G12 MD007600NINDS NIH HHS SC1 NS081726
6 · The paper itself

Abstract

After lesions to the mammalian optic nerve, the great majority of retinal ganglion cells (RGCs) die before their axons have even had a chance to regenerate. Frog RGCs, on the other hand, suffer only an approximately 50% cell loss, and we have previously investigated the mechanisms by which the application of growth factors can increase their survival rate. Retinoic acid (RA) is a vitamin A-derived lipophilic molecule that plays major roles during development of the nervous system. The RA signaling pathway is also present in parts of the adult nervous system, and components of it are upregulated after injury in peripheral nerves but not in the CNS. Here we investigate whether RA signaling affects long-term RGC survival at 6 weeks after axotomy. Intraocular injection of all-trans retinoic acid (ATRA), the retinoic acid receptor (RAR) type-α agonist AM80, the RARβ agonist CD2314, or the RARγ agonist CD1530, returned axotomized RGC numbers to almost normal levels. On the other hand, inhibition of RA synthesis with disulfiram, or of RAR receptors with the pan-RAR antagonist Ro-41-5253, or the RARβ antagonist LE135E, greatly reduced the survival of the axotomized neurons. Axotomy elicited a strong activation of the MAPK, STAT3 and AKT pathways; this activation was prevented by disulfiram or by RAR antagonists. Finally, addition of exogenous ATRA stimulated the activation of the first two of these pathways. Future experiments will investigate whether these strong survival-promoting effects of RA are mediated via the upregulation of neurotrophins.

Indexed as

AnimalsAnuraBenzoatesChromansNaphtholsNerve RegenerationOptic NerveOptic Nerve InjuriesReceptors, Retinoic AcidRetinal Ganglion CellsTetrahydronaphthalenesTretinoin4-(6-hydroxy-7-tricyclo(3.3.1.13,7)dec-1-yl-2-naphthalenyl)benzoic acidBenzoatesChromansNaphtholsReceptors, Retinoic AcidRo 41-5253tamibaroteneTetrahydronaphthalenesTretinoin

Identifiers

PMID27611191
PMCPMC5017682
OpenAlexW2507409852

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.