Evidence map›Paper›PMID 24198374›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

Development and plasticity of outer retinal circuitry following genetic removal of horizontal cells.

Patrick W Keeley, Gabriel Luna, Robert N Fariss, Kimberly A Skyles, Nils R Madsen, Mary A Raven, Ross A Poché, Eric C Swindell, Milan Jamrich, Edwin C Oh and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

29 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  4. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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  5. Review
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  10. Foxn4 is a temporal identity factor conferring mid/late-early retinal competence and involved in retinal synaptogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  11. Novel REEP6 gene mutation associated with autosomal recessive retinitis pigmentosa.Documenta ophthalmologica. Advances in ophthalmology · 2020
    Article
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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

13 authors at 8 institutions in 4 countries.

Patrick W KeeleyNeuroscience Research Institute, Department of Molecular, Cellular and Developmental Biology, Center for Bio-Image Informatics, Department of Electrical and Computer Engineering, and Department of Psychological and Brain Sciences, University of California, Santa Barbara, California 93106, Department of Molecular Physiology and Biophysics and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, Department of Pediatrics, University of Texas Medical School, Houston, Texas 77030, Department of Medicine, Division of Neurology, Center for Human Disease Modeling, Duke University Medical Center, Durham, North Carolina 27710, and Biological Imaging Core and Neurobiology-Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892.
Gabriel Luna
Robert N Fariss
Kimberly A Skyles
Nils R Madsen
Mary A Raven
Ross A Poché
Eric C Swindell
Milan Jamrich
Edwin C Oh
Anand Swaroop
Steven K Fisher
Benjamin E Reese
Bioscience Research · USBaylor College of Medicine · USDuke University · USInstitute of Molecular Biology and Biophysics · RUNational Institutes of Health · USTexas Medical Center · USThe University of Texas at Austin · USUniversity of California, Santa Barbara · US

Funding

Regulation of retinal developmentZIAEY000450 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2009 to 2025
$71.0M
Imaging Core UnitZICEY000459 · NEI · NATIONAL EYE INSTITUTE · PI FARISS, ROBERT · 2009 to 2025
$13.1M
Development of Retinal Bipolar CellsR01EY019968 · NEI · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI REESE, BENJAMIN E · 2010 to 2023
$4.9M
Two-Photon Microscopy for Biomedical ResearchS10RR022585 · NCRR · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI REESE, BENJAMIN E · 2007 to 2007
$500k
Spectral Laser Scanning Biological MicroscopeS10OD010610 · OD · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI RAVEN, MARY A · 2012 to 2012
$429k
Intramural NIH HHSNCRR NIH HHS S10 RR-022585NCRR NIH HHS S10 RR022585NEI NIH HHS R01 EY-019968NEI NIH HHS R01 EY019968NIH HHS S10 OD-010610NIH HHS S10 OD010610
6 · The paper itself

Abstract

The present study examined the consequences of eliminating horizontal cells from the outer retina during embryogenesis upon the organization and assembly of the outer plexiform layer (OPL). Retinal horizontal cells exhibit a migration defect in Lim1-conditional knock-out (Lim1-CKO) mice and become mispositioned in the inner retina before birth, redirecting their dendrites into the inner plexiform layer. The resultant (mature) OPL, developing in the absence of horizontal cells, shows a retraction of rod spherules into the outer nuclear layer and a sprouting of rod bipolar cell dendrites to reach ectopic ribbon-protein puncta. Cone pedicles and the dendrites of type 7 cone bipolar cells retain their characteristic stratification and colocalization within the collapsed OPL, although both are atrophic and the spatial distribution of the pedicles is disrupted. Developmental analysis of Lim1-CKO retina reveals that components of the rod and cone pathways initially co-assemble within their normal strata in the OPL, indicating that horizontal cells are not required for the correct targeting of photoreceptor terminals or bipolar cell dendrites. As the rod spherules begin to retract during the second postnatal week, rod bipolar cells initially show no signs of ectopic growth, sprouting only subsequently and continuing to do so well after the eighth postnatal week. These results demonstrate the critical yet distinctive roles for horizontal cells on the rod and cone pathways and highlight a unique and as-yet-unrecognized maintenance function of an inhibitory interneuron that is not required for the initial targeting and co-stratification of other components in the circuit.

Indexed as

AnimalsFemaleMiceMice, TransgenicNeuronal PlasticityRetinal Horizontal CellsRetinal NeuronsSynapsesVisual Pathways

Identifiers

PMID24198374
PMCPMC3818557
OpenAlexW2091989935

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.