Evidence map›Paper›PMID 22797304›Full record

ArticleThe Journal of clinical investigation2012

Inflammatory priming predisposes mice to age-related retinal degeneration.

Debarshi Mustafi, Tadao Maeda, Hideo Kohno, Joseph H Nadeau, Krzysztof Palczewski

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Genetic context modulates aging and degeneration in the murine retina.bioRxiv : the preprint server for biology · 2024
    Article
  5. Article
  6. Arrestin Facilitates Rhodopsin DephosphorylationThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  7. Article
  8. Frontiers in bioengineering and biotechnology · 2021
    Article
  9. mTORC1 Activation inOxidative medicine and cellular longevity · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Human aging and disease: Lessons from age-related macular degeneration.Proceedings of the National Academy of Sciences of the United States of America · 2018
    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

5 authors at 2 institutions in 2 countries.

Debarshi MustafiDepartment of Pharmacology, Case Western Reserve University, Cleveland, OH, USA.
Tadao Maeda
Hideo Kohno
Joseph H Nadeau
Krzysztof Palczewski
Case Western Reserve University · USInstitute for Systems Biology · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007250 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 1985 to 2023
$33.4M
TISSUE CULTURE AND HYBRIDOMA MODULEP30EY011373 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI Irina A Pikuleva · 1997 to 2026
$17.7M
REGULATION OF RHODOPSIN KINASE AND GUANYLATE CYCLASER01EY008061 · NEI · UNIVERSITY OF WASHINGTON · PI PALCZEWSKI, KRZYSZTOF · 1994 to 2014
$9.5M
MOUSE GENETIC RESOURCES FOR MULTIGENIC DISEASE ANALYSIS: AIDSP40RR012305 · NCRR · CASE WESTERN RESERVE UNIVERSITY · PI BERGER, NATHAN A. · 1996 to 2011
$6.8M
VISUAL SCIENCES TRAINING PROGRAMT32EY007157 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI Johannes Friedrich von Lintig · 2000 to 2026
$5.5M
Structural dissection of the visual signaling network in cone cellsR01EY019478 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI ENGEL, ANDREAS HERMANN, PALCZEWSKI, KRZYSZTOF · 2009 to 2013
$1.9M
Genetics and Therapy of Age-related Retinal Dysfunction in A/J MiceK08EY019880 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI MAEDA, TADAO · 2010 to 2013
$324k
RHODOPSIN KINASE: REGULATION, FUNCTION AND STRUCTURER29EY008061 · NEI · UNIVERSITY OF WASHINGTON · PI PALCZEWSKI, KRZYSZTOF NMI · 1989 to 1993
–
NCRR NIH HHS P40 RR012305NCRR NIH HHS RR12305NEI NIH HHS EY008061NEI NIH HHS EY019478NEI NIH HHS K08 EY019880NEI NIH HHS K08EY019880NEI NIH HHS P30 EY011373NEI NIH HHS P30 EY11373NEI NIH HHS R01 EY008061NEI NIH HHS R01 EY019478NEI NIH HHS T32 EY007157NEI NIH HHS T32EY007157NIGMS NIH HHS T32 GM007250NIGMS NIH HHS T32GM007250
6 · The paper itself

Abstract

Disruption of cellular processes affected by multiple genes and accumulation of numerous insults throughout life dictate the progression of age-related disorders, but their complex etiology is poorly understood. Postmitotic neurons, such as photoreceptor cells in the retina and epithelial cells in the adjacent retinal pigmented epithelium, are especially susceptible to cellular senescence, which contributes to age-related retinal degeneration (ARD). The multigenic and complex etiology of ARD in humans is reflected by the relative paucity of effective compounds for its early prevention and treatment. To understand the genetic differences that drive ARD pathogenesis, we studied A/J mice, which develop ARD more pronounced than that in other inbred mouse models. Although our investigation of consomic strains failed to identify a chromosome associated with the observed retinal deterioration, pathway analysis of RNA-Seq data from young mice prior to retinal pathological changes revealed that increased vulnerability to ARD in A/J mice was due to initially high levels of inflammatory factors and low levels of homeostatic neuroprotective factors. The genetic signatures of an uncompensated preinflammatory state and ARD progression identified here aid in understanding the susceptible genetic loci that underlie pathogenic mechanisms of age-associated disorders, including several human blinding diseases.

Indexed as

AgingAnimalsDisease Models, AnimalDisease ProgressionEye ProteinsHumansInflammationMiceMice, Inbred AMice, Inbred BALB CMice, Inbred StrainsMicroscopy, Electron, TransmissionRetinal DegenerationRetinal Pigment EpitheliumSpecies SpecificityEye Proteins

Identifiers

PMID22797304
PMCPMC3408755
OpenAlexW2027340310

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.