Evidence map›Paper›PMID 25446359›Full record

ReviewNeuroscience2015

The injury resistant ability of melanopsin-expressing intrinsically photosensitive retinal ganglion cells.

Q Cui, C Ren, P J Sollars, G E Pickard, K-F So

Open access · hybridAbstract readReview
In one paragraph

Review in Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

60 citing papers in PubMed, 112 citations in OpenAlex.

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  10. Frontiers in cell and developmental biology · 2025
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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

5 authors at 4 institutions in 3 countries.

Q CuiGuangdong-HongKong-Macau Institute of CNS Regeneration, Jinan University, Guangdong, PR China; Guangdong Medical Key Laboratory of Brain Function and Diseases, Jinan University, Guangzhou, PR China; GHM Collaboration and Innovation Center for Tissue Regeneration and Repair, Jinan University, Guangzhou, PR China.
C RenGuangdong-HongKong-Macau Institute of CNS Regeneration, Jinan University, Guangdong, PR China; Guangdong Medical Key Laboratory of Brain Function and Diseases, Jinan University, Guangzhou, PR China; GHM Collaboration and Innovation Center for Tissue Regeneration and Repair, Jinan University, Guangzhou, PR China.
P J SollarsSchool of Veterinary Medicine and Biomedical Sciences, University of Nebraska, Lincoln, NE 68583, USA.
G E PickardSchool of Veterinary Medicine and Biomedical Sciences, University of Nebraska, Lincoln, NE 68583, USA; Department of Ophthalmology and Visual Sciences, University of Nebraska Medical Center, Omaha, NE 68198, USA.
K-F SoGuangdong-HongKong-Macau Institute of CNS Regeneration, Jinan University, Guangdong, PR China; Guangdong Medical Key Laboratory of Brain Function and Diseases, Jinan University, Guangzhou, PR China; GHM Collaboration and Innovation Center for Tissue Regeneration and Repair, Jinan University, Guangzhou, PR China; Department of Ophthalmology, University of Hong Kong, Hong Kong. Electronic address: hrmaskf@hku.hk.
Jinan University · CNUniversity of Hong Kong · HKUniversity of Nebraska–Lincoln · USUniversity of Nebraska Medical Center · US

Funding

Homeostatic regulation of peripheral oscillators via autonomic circuitryR01NS077003 · NINDS · UNIVERSITY OF NEBRASKA LINCOLN · PI PICKARD, GARY EDWARD, SOLLARS, PATRICIA · 2012 to 2016
$1.8M
NINDS NIH HHS R01 NS077003NINDS NIH HHS R01NS077003
6 · The paper itself

Abstract

Neurons in the mammalian retina expressing the photopigment melanopsin have been identified as a class of intrinsically photosensitive retinal ganglion cells (ipRGCs). This discovery more than a decade ago has opened up an exciting new field of retinal research, and following the initial identification of photosensitive ganglion cells, several subtypes have been described. A number of studies have shown that ipRGCs subserve photoentrainment of circadian rhythms. They also influence other non-image forming functions of the visual system, such as the pupillary light reflex, sleep, cognition, mood, light aversion and development of the retina. These novel photosensitive neurons also influence form vision by contributing to contrast detection. Furthermore, studies have shown that ipRGCs are more injury-resistant following optic nerve injury, in animal models of glaucoma, and in patients with mitochondrial optic neuropathies, i.e., Leber's hereditary optic neuropathy and dominant optic atrophy. There is also an indication that these cells may be resistant to glutamate-induced excitotoxicity. Herein we provide an overview of ipRGCs and discuss the injury-resistant character of these neurons under certain pathological and experimental conditions.

Indexed as

AnimalsGlaucomaMelanopsinN-MethylaspartateOptic Nerve InjuriesRetinal Ganglion CellsRod OpsinsVisual PathwaysMelanopsinN-MethylaspartateRod Opsinsinjuryintrinsically photosensitive retinal ganglion cellmelanopsinsurvival

Identifiers

PMID25446359
PMCPMC4637166
OpenAlexW2095889022

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.