Evidence map›Paper›PMID 23281397›Full record

ArticleThe Journal of clinical investigation2013

Deimination restores inner retinal visual function in murine demyelinating disease.

Mabel Enriquez-Algeciras, Di Ding, Fabrizio G Mastronardi, Robert E Marc, Vittorio Porciatti, Sanjoy K Bhattacharya

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Mabel Enriquez-AlgecirasBascom Palmer Eye Institute, University of Miami, Miami, Florida, USA.
Di Ding
Fabrizio G Mastronardi
Robert E Marc
Vittorio Porciatti
Sanjoy K Bhattacharya
University of Miami · USMiami Dermatology and Laser Institute · US

Funding

University of Utah, Core Vision Research GrantP30EY014800 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI PAUL STEVEN BERNSTEIN · 2005 to 2026
$14.6M
Shared Equipment ModuleP30EY014801 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Victor L Perez · 2004 to 2026
$12.2M
STRUCTURAL NEUROCHEMISTRY OF RETINAL CIRCUITSR01EY002576 · NEI · UNIVERSITY OF UTAH · PI MARC, ROBERT E · 1985 to 2016
$8.0M
Retinal RemodelingR01EY015128 · NEI · UNIVERSITY OF UTAH · PI JONES, BRYAN WILLIAM · 2004 to 2021
$7.0M
TRABECULAR MESHWORK PROTEINS IN GLAUCOMAR01EY016112 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BHATTACHARYA, SANJOY K · 2006 to 2016
$3.7M
RETINAL GANGLION CELL PLASTICITY IN GLAUCOMAR01EY019077 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PORCIATTI, VITTORIO · 2009 to 2015
$2.1M
CRCNS: Large-scale computational reconstruction of three-dimensional neuralR01EB005832 · NIBIB · UNIVERSITY OF UTAH · PI TASDIZEN, TOLGA · 2005 to 2008
$1.1M
NEI NIH HHS EY014800NEI NIH HHS EY015128NEI NIH HHS EY016112NEI NIH HHS EY019077NEI NIH HHS EY02576NEI NIH HHS P30 EY014800NEI NIH HHS P30 EY014801NEI NIH HHS R01 EY002576NEI NIH HHS R01 EY015128NEI NIH HHS R01 EY016112NEI NIH HHS R01 EY019077NIBIB NIH HHS EB005832NIBIB NIH HHS R01 EB005832
6 · The paper itself

Abstract

Progressive loss of visual function frequently accompanies demyelinating diseases such as multiple sclerosis (MS) and is hypothesized to be the result of damage to the axons and soma of neurons. Here, we show that dendritic impairment is also involved in these diseases. Deimination, a posttranslational modification, was reduced in the retinal ganglion cell layer of MS patients and in a transgenic mouse model of MS (ND4 mice). Reduced deimination accompanied a decrease in inner retinal function in ND4 mice, indicating loss of vision. Local restoration of deimination dramatically improved retinal function and elongation of neurites in isolated neurons. Further, neurite length was decreased by downregulation of deimination or siRNA knockdown of the export-binding protein REF, a primary target for deimination in these cells. REF localized to dendrites and bound selective mRNAs and translation machinery to promote protein synthesis. Thus, protein deimination and dendritic outgrowth play key roles in visual function and may be a general feature of demyelinating diseases.

Indexed as

AgedAmino Acid SequenceAnimalsDemyelinating DiseasesDisease Models, AnimalGene Knockdown TechniquesHumansMaleMiceMice, TransgenicMolecular Sequence DataMultiple SclerosisNuclear ProteinsProtein Processing, Post-TranslationalRetinaRetinal Ganglion CellsNuclear ProteinsRefbp2 protein, mouseRNA-Binding ProteinsTranscription Factors

Identifiers

PMID23281397
PMCPMC3561814
OpenAlexW2031480747

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.