Evidence map›Paper›PMID 22895730›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

A retinal ganglion cell that can signal irradiance continuously for 10 hours.

Kwoon Y Wong

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

93 citing papers in PubMed, 166 citations in OpenAlex.

  1. Trial
  2. Review
  3. Divergence of Melanopsin's Intrinsic Properties and Downstream Actions.bioRxiv : the preprint server for biology · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. What can the eye see with melanopsin?Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Melanopsin enhances image persistence.Current biology : CB · 2023
    Article
  16. Article
  17. Article
  18. Article
  19. Tangled up in blue: Contribution of short-wavelength sensitive cones in human circadian photoentrainment.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  20. Review

33 more citing papers are in PubMed but not listed here.

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

1 author at 1 institution in 1 country.

Kwoon Y WongDepartment of Ophthalmology & Visual Sciences, University of Michigan, Ann Arbor, Michigan 48105, USA. kwoon@umich.edu
University of Michigan–Ann Arbor · US

Funding

VIVARIUM MODULEP30EY007003 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI David Antonetti · 1987 to 2026
$17.6M
Cross-talk between ganglion-cell photoreceptors and other neurons in the retinaR00EY018863 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WONG, KWOON Y. · 2010 to 2012
$700k
NEI NIH HHS P30 EY007003NEI NIH HHS R00 EY018863NEI NIH HHS R00 EY18863
6 · The paper itself

Abstract

A recently discovered type of mammalian retinal ganglion cell encodes environmental light intensity and mediates non-image-forming visual behaviors, such as the pupillary reflex and circadian photoentrainment. These intrinsically photosensitive retinal ganglion cells (ipRGCs) generate endogenous, melanopsin-based photoresponses as well as extrinsic, rod/cone-driven responses. Because the ipRGCs' light responses and the behaviors they control are both remarkably tonic, these cells have been hypothesized to be capable of irradiance detection lasting throughout the day. I tested this hypothesis by obtaining multielectrode-array recordings from ipRGCs in a novel rat eyecup preparation that enhances the regeneration of rod/cone photopigments. I found that 10 h constant light could continuously evoke action potentials in these ganglion cells under conditions that stimulated (1) only melanopsin, (2) mainly the rod input, and (3) both intrinsic and extrinsic responses. In response to a 10 h stimulus with gradual intensity changes to simulate sunrise and sunset, ipRGC firing rates slowly increased during the "sunrise" phase and slowly decreased during the "sunset" phase. Furthermore, I recorded from putative ipRGCs of melanopsin-knock-out mice and found that these cells retained the ability to respond in a sustained fashion to 20 min light steps, indicating that melanopsin is not required for such tonic responses. In conclusion, ipRGCs can signal light continuously for at least 10 h and can probably track gradual irradiance changes over the course of the day. These results further suggest that the photoreceptors and ON bipolar cells presynaptic to ipRGCs may be able to respond to light continuously for 10 h.

Indexed as

2-Amino-5-phosphonovalerateAction PotentialsAminobutyratesAnimalsExcitatory Amino Acid AgonistsExcitatory Amino Acid AntagonistsFemaleIn Vitro TechniquesLightLightingLight Signal TransductionMaleMelanopsinMiceMice, KnockoutPatch-Clamp Techniques2-amino-4-phosphonobutyric acid2-Amino-5-phosphonovalerateAminobutyratesExcitatory Amino Acid AgonistsExcitatory Amino Acid AntagonistsFG 9041MelanopsinQuinoxalinesRod Opsins

Identifiers

PMID22895730
PMCPMC3432977
OpenAlexW1968786793

What OpenQuestion 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 OpenQuestion graph.