Evidence map›Paper›PMID 15689562›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2005

Insulin receptor substrate 2 is essential for maturation and survival of photoreceptor cells.

Xianjin Yi, Markus Schubert, Neal S Peachey, Kiyoshi Suzuma, Deborah J Burks, Jake A Kushner, Izumi Suzuma, Christopher Cahill, Carrie L Flint, Matthew A Dow and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

33 citing papers in PubMed, 76 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Observational
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Neurodegeneration and neuroprotection in diabetic retinopathy.International journal of molecular sciences · 2013
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
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 6 institutions in 2 countries.

Xianjin YiHoward Hughes Medical Institute, Children's Hospital Boston, Boston, Massachusetts 02115, USA.
Markus Schubert
Neal S Peachey
Kiyoshi Suzuma
Deborah J Burks
Jake A Kushner
Izumi Suzuma
Christopher Cahill
Carrie L Flint
Matthew A Dow
Rebecca L Leshan
George L King
Morris F White
Howard Hughes Medical Institute · USHarvard University Press · USJoslin Diabetes Center · USCleveland Eye Clinic · USHarvard University · USUniversity of Cologne · DE

Funding

STRUCTURE AND FUNCTION OF THE IRS SIGNALING SYSTEMR01DK043808 · NIDDK · JOSLIN DIABETES CENTER · PI WHITE, MORRIS F. · 1991 to 2004
$1.7M
NIDDK NIH HHS R01 DK043808NIDDK NIH HHS R01 DK43808
6 · The paper itself

Abstract

Insulin receptor substrates (Irs-proteins) integrate signals from the insulin and insulin-like growth factor-1 (IGF1) receptors with other processes to control cellular growth, function, and survival. Here, we show that Irs2 promoted the maturation and survival of photoreceptors in the murine retina immediately after birth. Irs2 was mainly localized to the outer plexiform layer as well as to photoreceptor inner segments. It was also seen in ganglion cells and inner plexiform layer but in smaller amounts. Compared with control littermates, Irs2 knock-out mice lose 10% of their photoreceptors 1 week after birth and up to 50% by 2 weeks of age as a result of increased apoptosis. The surviving photoreceptor cells developed short organized segments, which displayed proportionally diminished but otherwise normal electrical function. However, IGF1-stimulated Akt phosphorylation was barely detected, and cleaved/activated caspase-3 was significantly elevated in isolated retinas of Irs2-/- mice. When diabetes was prevented, which allowed the Irs2-/- mice to survive for 2 years, most photoreceptor cells were lost by 16 months of age. Because apoptosis is the final common pathway in photoreceptor degeneration, pharmacological strategies that increase Irs2 expression or function in photoreceptor cells could be a general treatment for blinding diseases such as retinitis pigmentosa.

Indexed as

Age FactorsAnimalsAnimals, NewbornApoptosisCell SurvivalDiabetic RetinopathyEye ProteinsGene DeletionHomeodomain ProteinsHyperglycemiaHyperinsulinismInsulin-Like Growth Factor IInsulin Receptor Substrate ProteinsInsulin ResistanceIntracellular Signaling Peptides and ProteinsMiceEye ProteinsHomeodomain ProteinsInsulin-Like Growth Factor IInsulin Receptor Substrate ProteinsIntracellular Signaling Peptides and ProteinsIrs2 protein, mousepancreatic and duodenal homeobox 1 proteinPhosphoproteinsProtein Serine-Threonine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-aktTrans-Activators

Identifiers

PMID15689562
PMCPMC6725974
OpenAlexW2127109381

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.