Evidence map›Paper›PMID 36977418›Full record

ArticleCurrent biology : CB2023

Cones and cone pathways remain functional in advanced retinal degeneration.

Erika M Ellis, Antonio E Paniagua, Miranda L Scalabrino, Mishek Thapa, Jay Rathinavelu, Yuekan Jiao, David S Williams, Greg D Field, Gordon L Fain, Alapakkam P Sampath

Open access · greenAbstract read
In one paragraph

Article in Current biology : CB, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.8field-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

24 citing papers in PubMed, 31 citations in OpenAlex.

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  5. Cell therapy for age-related macular degeneration.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
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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

10 authors at 2 institutions in 1 country.

Erika M EllisDepartment of Ophthalmology and Jules Stein Eye Institute, University of California, Los Angeles, Los Angeles, CA 90095-7000, USA.
Antonio E PaniaguaDepartment of Ophthalmology and Jules Stein Eye Institute, University of California, Los Angeles, Los Angeles, CA 90095-7000, USA.
Miranda L ScalabrinoDepartment of Ophthalmology and Jules Stein Eye Institute, University of California, Los Angeles, Los Angeles, CA 90095-7000, USA; Department of Neurobiology, Duke University School of Medicine, Durham, NC 27710, USA.
Mishek ThapaDepartment of Ophthalmology and Jules Stein Eye Institute, University of California, Los Angeles, Los Angeles, CA 90095-7000, USA; Department of Neurobiology, Duke University School of Medicine, Durham, NC 27710, USA.
Jay RathinaveluDepartment of Neurobiology, Duke University School of Medicine, Durham, NC 27710, USA.
Yuekan JiaoDepartment of Ophthalmology and Jules Stein Eye Institute, University of California, Los Angeles, Los Angeles, CA 90095-7000, USA.
David S WilliamsDepartment of Ophthalmology and Jules Stein Eye Institute, University of California, Los Angeles, Los Angeles, CA 90095-7000, USA. Electronic address: dswilliams@g.ucla.edu.
Greg D FieldDepartment of Ophthalmology and Jules Stein Eye Institute, University of California, Los Angeles, Los Angeles, CA 90095-7000, USA; Department of Neurobiology, Duke University School of Medicine, Durham, NC 27710, USA. Electronic address: gfield@mednet.ucla.edu.
Gordon L FainDepartment of Ophthalmology and Jules Stein Eye Institute, University of California, Los Angeles, Los Angeles, CA 90095-7000, USA. Electronic address: gfain@ucla.edu.
Alapakkam P SampathDepartment of Ophthalmology and Jules Stein Eye Institute, University of California, Los Angeles, Los Angeles, CA 90095-7000, USA. Electronic address: asampath@jsei.ucla.edu.
University of California, Los Angeles · USDuke University · US

Funding

VISION RESEARCHP30EY005722 · NEI · DUKE UNIVERSITY · PI Vadim Y Arshavsky · 1985 to 2026
$19.3M
Vision Research Core at UCLAP30EY000331 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Xian-Jie Yang · 1985 to 2026
$16.8M
PHYSIOLOGY OF PHOTORECEPTORSR01EY001844 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GORDON Lee FAIN · 1985 to 2026
$9.9M
Analyses of retinal circuits after rod rescue in a mouse model of human blindnessR01EY027193 · NEI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHEN, JEANNIE, FIELD, GREGORY DARIN · 2016 to 2020
$2.7M
RPE cell biology, aging, and diseaseR01EY027442 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WILLIAMS, DAVID S · 2017 to 2021
$2.6M
Molecular Mechanisms of Photoreceptor AdaptationR01EY029817 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SAMPATH, ALAPAKKAM P · 2019 to 2023
$2.1M
Cellular Mechanisms of Photoreceptor Disk MorphogenesisR01EY033035 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WILLIAMS, DAVID S · 2022 to 2025
$1.8M
MOLECULAR GENETICS OF EARLY EYE DEVELOPMENTZ01EY000311 · NEI · NATIONAL EYE INSTITUTE · PI TOMAREV, STANISLAV I · 1996 to 2008
$941k
Intramural NIH HHS Z01 EY000311NEI NIH HHS P30 EY000331NEI NIH HHS P30 EY005722NEI NIH HHS R01 EY001844NEI NIH HHS R01 EY027193NEI NIH HHS R01 EY027442NEI NIH HHS R01 EY029817NEI NIH HHS R01 EY033035
6 · The paper itself

Abstract

Most defects causing retinal degeneration in retinitis pigmentosa (RP) are rod-specific mutations, but the subsequent degeneration of cones, which produces loss of daylight vision and high-acuity perception, is the most debilitating feature of the disease. To understand better why cones degenerate and how cone vision might be restored, we have made the first single-cell recordings of light responses from degenerating cones and retinal interneurons after most rods have died and cones have lost their outer-segment disk membranes and synaptic pedicles. We show that degenerating cones have functional cyclic-nucleotide-gated channels and can continue to give light responses, apparently produced by opsin localized either to small areas of organized membrane near the ciliary axoneme or distributed throughout the inner segment. Light responses of second-order horizontal and bipolar cells are less sensitive but otherwise resemble those of normal retina. Furthermore, retinal output as reflected in responses of ganglion cells is less sensitive but maintains spatiotemporal receptive fields at cone-mediated light levels. Together, these findings show that cones and their retinal pathways can remain functional even as degeneration is progressing, an encouraging result for future research aimed at enhancing the light sensitivity of residual cones to restore vision in patients with genetically inherited retinal degeneration.

Indexed as

Color VisionRetinal DegenerationRetinitis PigmentosaHumansRetinaRetinal Cone Photoreceptor Cellsdegenerationphotoreceptorrd10retinaretinal ganglion cellretinitis pigmentosa

Identifiers

PMID36977418
PMCPMC10133175
OpenAlexW4361002069

What OpenQuestion holds

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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.