Evidence map›Paper›PMID 25118265›Full record

ArticleInvestigative ophthalmology & visual science2014

Loss of outer retinal neurons and circuitry alterations in the DBA/2J mouse.

Laura Fernández-Sánchez, Luis Pérez de Sevilla Müller, Nicholas C Brecha, Nicolás Cuenca

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

  1. Article
  2. Article
  3. The Variety of Mechanosensitive Ion Channels in Retinal Neurons.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Autophagy · 2023
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. A Robust Microbead Occlusion Model of Glaucoma for the Common Marmoset.Translational vision science & technology · 2022
    Article
  13. Article
  14. Article
  15. Activation of Apoptosis in a βB1-CTGF Transgenic Mouse Model.International journal of molecular sciences · 2021
    Article
  16. BrdU Positive Cells Induced in a Genetic Mouse Model of Glaucoma.Journal of ophthalmology & visual sciences · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. Article
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

4 authors.

Laura Fernández-SánchezDepartment of Physiology, Genetics, and Microbiology, University of Alicante, San Vicente del Raspeig, Spain.
Luis Pérez de Sevilla MüllerDepartment of Neurobiology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, United States.
Nicholas C BrechaDepartment of Neurobiology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, United States.
Nicolás CuencaDepartment of Physiology, Genetics, and Microbiology, University of Alicante, San Vicente del Raspeig, Spain.

Funding

Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
NEUROCHEMICAL PATHWAYS IN THE INNER RETINAR01EY004067 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BRECHA, NICHOLAS C. · 1985 to 2019
$9.0M
Neurochemical Pathways in the Inner RetinaR56EY004067 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BRECHA, NICHOLAS C. · 2009 to 2009
$462k
Regulation of Calcium Signaling in Retinal Ganglion Cells after Nerve InjuryI01BX000764 · VA · VA GREATER LOS ANGELES HEALTHCARE SYSTEM · PI BRECHA, NICHOLAS C. · 2011 to 2020
–
BLRD VA I01 BX000764NEI NIH HHS EY04067NEI NIH HHS R01 EY004067NEI NIH HHS R56 EY004067NIDDK NIH HHS P30 DK041301NIDDK NIH HHS P30 DK41301
6 · The paper itself

Abstract

purposeThe DBA/2J mouse line develops essential iris atrophy, pigment dispersion, and glaucomatous age-related changes, including an increase of IOP, optic nerve atrophy, and retinal ganglion cell (RGC) death. The aim of this study was to evaluate possible morphological changes in the outer retina of the DBA/2J mouse concomitant with disease progression and aging, based on the reduction of both the a- and b-waves and photopic flicker ERGs in this mouse line.

methodsVertically sectioned DBA/2J mice retinas were evaluated at 3, 8, and 16 months of age using photoreceptor, horizontal, and bipolar cell markers. Sixteen-month-old C57BL/6 mice retinas were used as controls.

resultsThe DBA/2J mice had outer retinal degeneration at all ages, with the most severe degeneration in the oldest retinas. At 3 months of age, the number of photoreceptor cells and the thickness of the OPL were reduced. In addition, there was a loss of horizontal and ON-bipolar cell processes. At 8 months of age, RGC degeneration occurred in patches, and in the outer retina overlying these patches, cone morphology was impaired with a reduction in size as well as loss of outer segments and growth of horizontal and bipolar cell processes into the outer nuclear layer. At 16 months of age, connectivity between photoreceptors and horizontal and bipolar cell processes overlying these patches was lost.

conclusionsRetinal degeneration in DBA/2J mice includes photoreceptor death, loss of bipolar and horizontal cell processes, and loss of synaptic contacts in an aging-dependent manner.

Indexed as

AnimalsApoptosisDisease Models, AnimalElectroretinographyFemaleGlaucomaIntraocular PressureIrisLightMiceMice, Inbred C57BLMice, Inbred DBAMice, Mutant StrainsPhotoreceptor Cells, VertebrateRetinaRetinal Bipolar Cellsbipolar cellglaucomahorizontal cellphotoreceptorretinal degenerationsynaptic triad

Identifiers

PMID25118265
PMCPMC4176418

What OpenQuestion holds

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Registered trials

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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.