Evidence map›Paper›PMID 30176221›Full record

ArticleExperimental eye research2018

Comparative proteomic analysis of normal and gliotic PVR retina and contribution of Müller glia to this profile.

Karen Eastlake, Wendy E Heywood, Phillip Banerjee, Emily Bliss, Kevin Mills, Peng T Khaw, David Charteris, G Astrid Limb

Open access · hybridAbstract read
In one paragraph

Article in Experimental eye research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  8. Cell-Based Therapies for Glaucoma.Translational vision science & technology · 2023
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  9. Mass spectrometry-based retina proteomics.Mass spectrometry reviews · 2023
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. The Proteome of Preretinal Tissue in Proliferative Vitreoretinopathy.Ophthalmic surgery, lasers & imaging retina · 2021
    Article
  15. Article
  16. Review
  17. 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

8 authors at 3 institutions in 1 country.

Karen EastlakeNIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK.
Wendy E HeywoodCentre for Translational Omics, UCL Great Ormond Street Institute of Child Health, London, UK.
Phillip BanerjeeNIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK.
Emily BlissCentre for Translational Omics, UCL Great Ormond Street Institute of Child Health, London, UK.
Kevin MillsCentre for Translational Omics, UCL Great Ormond Street Institute of Child Health, London, UK.
Peng T KhawNIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK.
David CharterisNIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK.
G Astrid LimbNIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK. Electronic address: g.limb@ucl.ac.uk.
Moorfields Eye Hospital · GBGreat Ormond Street Hospital · GBNational Institute for Health Research · GB

Funding

Medical Research Council MR/K008722/1Medical Research Council MR/P01660X/1
6 · The paper itself

Abstract

Müller glia are responsible for the neural retina regeneration observed in fish and amphibians throughout life. Despite the presence of these cells in the adult human retina, there is no evidence of regeneration occurring in humans following disease or injury. It may be possible that factors present in the degenerated retina could prevent human Müller glia from proliferating and neurally differentiating within the diseased retina. On this basis, investigations into the proteomic profile of these cells and the abundance of key proteins associated to Müller glia in the gliotic PVR retina, may assist in the identification of factors with the potential to control Müller proliferation and neural differentiation in vivo. Label free mass spectrometry identified 1527 proteins in Müller glial cell preparations, 1631 proteins in normal retina and 1074 in gliotic PVR retina. Compared to normal retina, 28 proteins were upregulated and 196 proteins downregulated by 2-fold or more in the gliotic PVR retina. As determined by comparative proteomic analyses, of the proteins highly upregulated in the gliotic PVR retina, the most highly abundant proteins in Müller cell lysates included vimentin, GFAP, polyubiquitin and HSP90a. The observations that proteins highly upregulated in the gliotic retina constitute major proteins expressed by Müller glia provide the basis for further studies into mechanisms that regulate their production. In addition investigations aimed at controlling the expression of these proteins may aid in the identification of factors that could potentially promote endogenous regeneration of the adult human retina after disease or injury.

Indexed as

AdultAgedAged, 80 and overBlotting, WesternCells, CulturedElectrophoresis, Gel, Two-DimensionalEye ProteinsFemaleGliosisHumansImmunohistochemistryMaleMiddle AgedNerve RegenerationNeurogliaProteomicsEye ProteinsMüller gliaProteomicsRetina degenerationRetinal gliosis

Identifiers

PMID30176221
PMCPMC6280037
OpenAlexW2889478730

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.