Evidence map›Paper›PMID 22238088›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

Preservation of cone photoreceptors after a rapid yet transient degeneration and remodeling in cone-only Nrl-/- mouse retina.

Jerome E Roger, Keerthi Ranganath, Lian Zhao, Radu I Cojocaru, Matthew Brooks, Norimoto Gotoh, Shobi Veleri, Avinash Hiriyanna, Rivka A Rachel, Maria Mercedes Campos and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

41 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Gene therapy rescues cone function inMolecular therapy. Advances · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. NRLStem cells (Dayton, Ohio) · 2021
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. 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

13 authors at 1 institution in 1 country.

Jerome E RogerNeurobiology-Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Keerthi Ranganath
Lian Zhao
Radu I Cojocaru
Matthew Brooks
Norimoto Gotoh
Shobi Veleri
Avinash Hiriyanna
Rivka A Rachel
Maria Mercedes Campos
Robert N Fariss
Wai T Wong
Anand Swaroop
National Institutes of Health · US

Funding

Regulation of retinal developmentZIAEY000450 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2009 to 2025
$71.0M
Retinal aging and inherited neurodegenerative diseasesZIAEY000473 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2009 to 2014
$16.2M
Imaging Core UnitZICEY000459 · NEI · NATIONAL EYE INSTITUTE · PI FARISS, ROBERT · 2009 to 2025
$13.1M
Neuronal differentiation in the retinaZIAEY000451 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2009 to 2011
$8.0M
Dynamic Imaging of Retinal MicrogliaZIAEY000463 · NEI · NATIONAL EYE INSTITUTE · PI WONG, WAI · 2009 to 2020
$7.3M
Microglial Inhibition as a Therapeutic Strategy for Subretinal HemorrhageZIAEY000505 · NEI · NATIONAL EYE INSTITUTE · PI WONG, WAI · 2011 to 2019
$1.9M
Intramural NIH HHS ZIA EY000450Intramural NIH HHS ZIA EY000451Intramural NIH HHS ZIA EY000473
6 · The paper itself

Abstract

Cone photoreceptors are the primary initiator of visual transduction in the human retina. Dysfunction or death of rod photoreceptors precedes cone loss in many retinal and macular degenerative diseases, suggesting a rod-dependent trophic support for cone survival. Rod differentiation and homeostasis are dependent on the basic motif leucine zipper transcription factor neural retina leucine zipper (NRL). The loss of Nrl (Nrl(-/-)) in mice results in a retina with predominantly S-opsin-containing cones that exhibit molecular and functional characteristics of wild-type cones. Here, we report that Nrl(-/-) retina undergoes a rapid but transient period of degeneration in early adulthood, with cone apoptosis, retinal detachment, alterations in retinal vessel structure, and activation and translocation of retinal microglia. However, cone degeneration stabilizes by 4 months of age, resulting in a thinner but intact outer nuclear layer with residual cones expressing S- and M-opsins and a preserved photopic electroretinogram. At this stage, microglia translocate back to the inner retina and reacquire a quiescent morphology. Gene profiling analysis during the period of transient degeneration reveals misregulation of genes related to stress response and inflammation, implying their involvement in cone death. The Nrl(-/-) mouse illustrates the long-term viability of cones in the absence of rods and retinal pigment epithelium defects in a rodless retina. We propose that Nrl(-/-) retina may serve as a model for elucidating mechanisms of cone homeostasis and degeneration that would be relevant to understanding diseases of the cone-dominant human macula.

Indexed as

AnimalsApoptosisBasic-Leucine Zipper Transcription FactorsDisease Models, AnimalEye ProteinsFemaleMaleMiceMice, Inbred C57BLMice, KnockoutRetinaRetinal Cone Photoreceptor CellsRetinal DegenerationRetinal DetachmentBasic-Leucine Zipper Transcription FactorsEye ProteinsNrl protein, mouse

Identifiers

PMID22238088
PMCPMC3567450
OpenAlexW1998915457

What OpenQuestion holds

Textmetadata
LicenceTDM
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.