Evidence map›Paper›PMID 26284544›Full record

ArticleInvestigative ophthalmology & visual science2015

Visual Cone Arrestin 4 Contributes to Visual Function and Cone Health.

Janise D Deming, Joseph S Pak, Bruce M Brown, Moon K Kim, Moe H Aung, Yun Sung Eom, Jung-A Shin, Eun-Jin Lee, Machelle T Pardue, Cheryl Mae Craft

Open access · hybridAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.5field-weighted citation impact, top 18% 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, 38 citations in OpenAlex.

  1. Zoological research · 2026
    Article
  2. Article
  3. Advances in the study of ARR3 in myopia.Frontiers in cell and developmental biology · 2025
    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

10 authors at 4 institutions in 2 countries.

Janise D DemingMary D. Allen Laboratory for Vision Research, USC Eye Institute, Department of Ophthalmology, Keck School of Medicine of the University of Southern California, Los Angeles, California, United States.
Joseph S PakMary D. Allen Laboratory for Vision Research, USC Eye Institute, Department of Ophthalmology, Keck School of Medicine of the University of Southern California, Los Angeles, California, United States.
Bruce M BrownMary D. Allen Laboratory for Vision Research, USC Eye Institute, Department of Ophthalmology, Keck School of Medicine of the University of Southern California, Los Angeles, California, United States.
Moon K KimRehabilitation Research & Development Center of Excellence, Atlanta VA Medical Center, Decatur, Georgia, United States.
Moe H AungNeuroscience/Ophthalmology, Emory University, Atlanta, Georgia, United States.
Yun Sung EomMary D. Allen Laboratory for Vision Research, USC Eye Institute, Department of Ophthalmology, Keck School of Medicine of the University of Southern California, Los Angeles, California, United States 4Dornsife College of Letters, Arts and Sciences, Univers.
Jung-A ShinMary D. Allen Laboratory for Vision Research, USC Eye Institute, Department of Ophthalmology, Keck School of Medicine of the University of Southern California, Los Angeles, California, United States 5Department of Anatomy, School of Medicine, Ewha Womans.
Eun-Jin LeeMary D. Allen Laboratory for Vision Research, USC Eye Institute, Department of Ophthalmology, Keck School of Medicine of the University of Southern California, Los Angeles, California, United States 6Department of Biomedical Engineering, University of Sou.
Machelle T PardueRehabilitation Research & Development Center of Excellence, Atlanta VA Medical Center, Decatur, Georgia, United States 3Neuroscience/Ophthalmology, Emory University, Atlanta, Georgia, United States.
Cheryl Mae CraftMary D. Allen Laboratory for Vision Research, USC Eye Institute, Department of Ophthalmology, Keck School of Medicine of the University of Southern California, Los Angeles, California, United States 7Department of Cell & Neurobiology, Keck School of Medic.
University of Southern California · USSouthern California Eye Institute · USAtlanta VA Medical Center · USEmory University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008169 · NIGMS · EMORY UNIVERSITY · PI GROSS, ROBERT E · 1987 to 2021
$20.3M
VISION RESEARCHP30EY003040 · NEI · DOHENY EYE INSTITUTE · PI SUN, DEMING · 1985 to 2013
$7.0M
Retinal Mechanisms of Refractive DevelopmentR01EY016435 · NEI · GEORGIA INSTITUTE OF TECHNOLOGY · PI Machelle T. Pardue · 2009 to 2026
$5.4M
Mechanisms of Cone Pigment DeactivationR01EY015851 · NEI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CRAFT, CHERYL MAE · 2005 to 2009
$1.8M
NEI NIH HHS EY03040NEI NIH HHS P30 EY003040NEI NIH HHS R01 EY015851NEI NIH HHS R01-EY015851NEI NIH HHS R01 EY016435NEI NIH HHS R01-EY016435NIGMS NIH HHS T32 GM008169
6 · The paper itself

Abstract

purposeVisual arrestins (ARR) play a critical role in shutoff of rod and cone phototransduction. When electrophysiological responses are measured for a single mouse cone photoreceptor, ARR1 expression can substitute for ARR4 in cone pigment desensitization; however, each arrestin may also contribute its own, unique role to modulate other cellular functions.

methodsA combination of ERG, optokinetic tracking, immunohistochemistry, and immunoblot analysis was used to investigate the retinal phenotypes of Arr4 null mice (Arr4-/-) compared with age-matched control, wild-type mice.

resultsWhen 2-month-old Arr4-/- mice were compared with wild-type mice, they had diminished visual acuity and contrast sensitivity, yet enhanced ERG flicker response and higher photopic ERG b-wave amplitudes. In contrast, in older Arr4-/- mice, all ERG amplitudes were significantly reduced in magnitude compared with age-matched controls. Furthermore, in older Arr4-/- mice, the total cone numbers decreased and cone opsin protein immunoreactive expression levels were significantly reduced, while overall photoreceptor outer nuclear layer thickness was unchanged.

conclusionsOur study demonstrates that Arr4-/- mice display distinct phenotypic differences when compared to controls, suggesting that ARR4 modulates essential functions in high acuity vision and downstream cellular signaling pathways that are not fulfilled or substituted by the coexpression of ARR1, despite its high expression levels in all mouse cones. Without normal ARR4 expression levels, cones slowly degenerate with increasing age, making this a new model to study age-related cone dystrophy.

Indexed as

Gene Expression RegulationAnimalsArrestinCell CountDisease Models, AnimalDNAElectroretinographyImmunoblottingImmunohistochemistryLight Signal TransductionMiceMice, Inbred C57BLMice, KnockoutMicroscopy, ConfocalPhenotypeRetinal Cone Photoreceptor CellsArrestinDNA

Identifiers

PMID26284544
PMCPMC4544185
OpenAlexW1580572370

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.