Evidence map›Paper›PMID 23936334›Full record

ArticlePloS one2013

Serum TRPM1 autoantibodies from melanoma associated retinopathy patients enter retinal on-bipolar cells and attenuate the electroretinogram in mice.

Wei-Hong Xiong, Robert M Duvoisin, Grazyna Adamus, Brett G Jeffrey, Celia Gellman, Catherine W Morgans

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. American journal of ophthalmology case reports · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  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

6 authors at 2 institutions in 1 country.

Wei-Hong XiongCasey Eye Institute, Oregon Health & Science University, Portland, Oregon, USA.
Robert M Duvoisin
Grazyna Adamus
Brett G Jeffrey
Celia Gellman
Catherine W Morgans
Oregon Health & Science University · USNational Institutes of Health · US

Funding

Proteomics CoreP30EY010572 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Kate E Keller · 1995 to 2026
$19.4M
Effects of autoantibodies on synaptic transmission in the retinaR01EY022369 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI MORGANS, CATHERINE W · 2013 to 2016
$1.9M
Signaling mechanisms of retinal bipolar cellsR01EY018625 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI MORGANS, CATHERINE W · 2009 to 2012
$1.5M
NEI NIH HHS NIH5P30EY010572NEI NIH HHS NIHR01EY018625NEI NIH HHS NIHR01EY022369NEI NIH HHS P30 EY010572NEI NIH HHS R01 EY018625NEI NIH HHS R01 EY022369
6 · The paper itself

Abstract

Melanoma-associated retinopathy (MAR) is a paraneoplastic syndrome associated with cutaneous malignant melanoma and the presence of autoantibodies that label neurons in the inner retina. The visual symptoms and electroretinogram (ERG) phenotype characteristic of MAR resemble the congenital visual disease caused by mutations in TRPM1, a cation channel expressed by both melanocytes and retinal bipolar cells. Four serum samples from MAR patients were identified as TRPM1 immunoreactive by 1. Labeling of ON-bipolar cells in TRPM1+/+ but not TRPM1-/- mouse retina, 2. Labeling of TRPM1-transfected CHO cells; and 3. Attenuation of the ERG b-wave following intravitreal injection of TRPM1-positive MAR IgG into wild-type mouse eyes, and the appearance of the IgG in the retinal bipolar cells at the conclusion of the experiment. Furthermore, the epitope targeted by the MAR autoantibodies was localized within the amino-terminal cytoplasmic domain of TRPM1. Incubation of live retinal neurons with TRPM1-positive MAR serum resulted in the selective accumulation of IgG in ON-bipolar cells from TRPM1+/+ mice, but not TRPM1-/- mice, suggesting that the visual deficits in MAR are caused by the uptake of TRPM1 autoantibodies into ON-bipolar cells, where they bind to an intracellular epitope of the channel and reduce the ON-bipolar cell response to light.

Indexed as

AnimalsAutoantibodiesCell SurvivalCytoplasmElectroretinographyEpitopesHumansImmunoglobulin GMiceMice, Inbred C57BLParaneoplastic Syndromes, OcularProtein Structure, TertiaryProtein TransportRetinal Bipolar CellsTRPM Cation ChannelsAutoantibodiesEpitopesImmunoglobulin GTRPM1 protein, humanTRPM Cation Channels

Identifiers

PMID23936334
PMCPMC3731326
OpenAlexW1965658868

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.