Evidence map›Paper›PMID 19941335›Full record

ArticleGlia2010

A novel type of glial cell in the retina is stimulated by insulin-like growth factor 1 and may exacerbate damage to neurons and Müller glia.

Andy J Fischer, Melissa A Scott, Christopher Zelinka, Patrick Sherwood

Abstract read
In one paragraph

Article in Glia, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing 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

46 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Early-stage diabetic retinopathy: gut-metabolic triggers, immune-neurodegeneration, and interventions.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2025
    Review
  3. Article
  4. Article
  5. Retinal glia in myopia: current understanding and future directions.Frontiers in cell and developmental biology · 2024
    Review
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  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Observational
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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

4 authors at 1 institution in 1 country.

Andy J FischerDepartment of Neuroscience, The Ohio State University, College of Medicine, Columbus, OH 43210-1239, USA. fischer.412@osu.edu
Melissa A Scott
Christopher Zelinka
Patrick Sherwood
The Ohio State University · US

Funding

Muller glia and neuronal regeneration in the retinaR01EY016043 · NEI · OHIO STATE UNIVERSITY · PI FISCHER, ANDY J · 2006 to 2009
$1.2M
NEI NIH HHS EY016043NEI NIH HHS R01 EY016043
6 · The paper itself

Abstract

Recent studies have demonstrated that insulin can have profound affects on the survival of neurons within the retina. The purpose of this study was to determine how insulin-like growth factor 1 (IGF1) influences retinal cells; in particular, the glial cells. We identify a novel type of glial cell in the avian retina and provide evidence that these cells can respond to acute damage and IGF1. In normal retinas, we found a distinct cell-type, scattered across the ganglion cell and inner plexiform layers that express Sox2, Sox9, Nkx2.2, vimentin, and transitin, the avian homologue of mammalian nestin. These glial cells have a unique immunohistochemical profile, morphology, and distribution that are distinct among other known types of retinal glia, including microglia, oligodendrocytes, astrocytes, and Muller glia. We termed these cells nonastrocytic inner retinal glia-like (NIRG) cells. We found that the NIRG cells may express the IGF1 receptor and respond to IGF1 by proliferating, migrating distally into the retina, and upregulating transitin. In addition, IGF1 stimulated microglia to become reactive and upregulate lysosomal membrane glycoprotein and CD45. With microglia and NIRG cells stimulated by IGF1 there were elevated levels of cell death and numerous focal detachments across the retina in response to excitotoxic damage. Cell death was prominent within the areas of detachment coinciding with a stark loss of Müller glia and accumulation of NIRG cells. We conclude that NIRG cells are a novel type of retinal glia that is sensitive to IGF1 and whose activity may impact the survival of neurons and Müller glia.

Indexed as

AnimalsAnimals, NewbornCell CountCell ProliferationChickensDrug SynergismExcitatory Amino Acid AgonistsGlial Fibrillary Acidic ProteinHomeobox Protein Nkx-2.2Homeodomain ProteinsInjections, IntraocularIn Situ Nick-End LabelingInsulin-Like Growth Factor ILeukocyte Common AntigensNeurogliaNeuronsExcitatory Amino Acid AgonistsGlial Fibrillary Acidic ProteinHomeobox Protein Nkx-2.2Homeodomain ProteinsInsulin-Like Growth Factor ILeukocyte Common Antigensnkx2.2b protein, zebrafishN-MethylaspartatePlant LectinsReceptor, IGF Type 1Receptor, IGF Type 2Ricinus communis agglutinin-1SOX Transcription FactorsTranscription FactorsVimentinZebrafish Proteins

Identifiers

PMID19941335
PMCPMC2830337
OpenAlexW1987865684

What Socratic 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 Socratic graph.