Evidence map›Paper›PMID 41507222›Full record

ArticleScientific reports2026

Neuropsin-expressing cells in the retina affect melanopsin expression and response to light in mice.

Hugo Calligaro, Brian Khov, Keun-Young Kim, Hiep Le, Mark Ellisman, Satchidananda Panda

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Hugo CalligaroSalk Institute for Biological Studies, La Jolla, CA, 92037, USA.
Brian KhovSalk Institute for Biological Studies, La Jolla, CA, 92037, USA.
Keun-Young KimDepartment of Neurosciences, University of California at San Diego School of Medicine, La Jolla, CA, 92161, USA.
Hiep LeSalk Institute for Biological Studies, La Jolla, CA, 92037, USA.
Mark EllismanDepartment of Neurosciences, University of California at San Diego School of Medicine, La Jolla, CA, 92161, USA.
Satchidananda PandaSalk Institute for Biological Studies, La Jolla, CA, 92037, USA. panda@salk.edu.

Funding

National Center for Microscopy and Imaging Research: A BRAIN Technology Integration and Dissemination ResourceU24NS120055 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELLISMAN, MARK H · 2021 to 2025
$5.4M
Support of and Extensions to the Cell Image LibraryR01GM082949 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELLISMAN, MARK H · 2007 to 2019
$4.1M
The National Center for Microscopy and Imaging Research, a Community-wide Scientific ResourceR24GM137200 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELLISMAN, MARK H · 2020 to 2022
$3.0M
FEI TITAN HALO 300kV INTERMEDIATE VOLTAGE ELECTRON MICROSCOPES10OD021784 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELLISMAN, MARK H · 2017 to 2017
$1.9M
National Science Foundation NSF2014862-UTA20-000890NIGMS NIH HHS R01 GM082949NIGMS NIH HHS R24 GM137200NIH HHS S10 OD021784NIH HHS U24 NS120055, R24GM137200, 1S10OD021784NINDS NIH HHS U24 NS120055
6 · The paper itself

Abstract

Neuropsin (OPN5) is an opsin involved in several non-image forming functions in the retina, such as the photoentrainment of the retinal circadian clock. These roles were previously attributed to melanopsin (OPN4) which prompted the hypothesis that OPN4 and OPN5 functionally interact. However, the specific cells expressing OPN5 and their interactions with the broader photoreception system remain unclear. This study aims to characterize OPN5-expressing cells and assess how their absence influences the photoresponses of OPN4-expressing cells. Through the use of genetically encoded reporters, confocal microscopy and serial blockface electron microscopy, we identified and reconstructed OPN5-cells and their processes. OPN5 expression was found in a small number of various retinal ganglion cell (RGC) subtypes, without overlap with OPN4-expressing cells, and presented distinct dendritic arborization patterns. In parallel, we measured the retinal electrical response to light in mice lacking either OPN4 or OPN5 to determine the contribution of each opsin and the consequences of their absence. Mice deficient in OPN5 exhibited reduced maximal discharge rates upon stimulation of light, though response duration remained unchanged. No specific electrical response to UV light was detected in OPN5-expressing cells suggesting that the response of OPN5 cells to light is translated in non-electrical pathway.

Indexed as

LightRetinaRetinal Ganglion CellsRod OpsinsAnimalsMelanopsinMembrane ProteinsMiceOpsinsMelanopsinMembrane ProteinsOPN5 protein, mouseOpsinsRod Opsins

Identifiers

PMID41507222
PMCPMC12783770

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Registered trials

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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.