# Light and myopia: a focus on the expanding role of non-visual opsins

**Authors:** Kate Gettinger, Kazuo Tsubota, Kazuno Negishi, Toshihide Kurihara

PMC · DOI: 10.1186/s40662-025-00472-y · Eye and Vision · 2026-01-31

## TL;DR

This paper reviews how non-visual opsins may influence myopia and could lead to new treatment strategies.

## Contribution

The paper highlights the emerging role of non-visual opsins in myopia regulation and their potential for future treatments.

## Key findings

- Non-visual opsins OPN3, OPN4, and OPN5 are potentially involved in regulating myopia.
- Current understanding of non-visual opsins could inform new treatment strategies for myopia.

## Abstract

Myopia, or near-sightedness, is a growing global concern as its incidence rate continues to dramatically rise. It has been linked to significant ocular morbidity and reduced quality of life. Despite this, much is still largely unknown about the development of and the mechanisms driving the pathogenesis of myopia. As such, myopia prevention and myopia mitigation treatment strategies are occasionally ineffective, can be difficult to adhere to, and have diminishing returns over time. Recently, non-visual opsins (OPN3, OPN4, and OPN5) have emerged as potentially impacting myopia regulation. This narrative review aims to summarize the current understanding of the non-visual opsins and how they might influence myopia. In addition, this review explores how utilizing this knowledge can help develop promising future treatment strategies to reduce the incidence and severity of myopia.

## Linked entities

- **Genes:** OPN3 (opsin 3) [NCBI Gene 23596], OPN4 (opsin 4) [NCBI Gene 94233], OPN5 (opsin 5) [NCBI Gene 221391]
- **Diseases:** myopia (MONDO:0001384)

## Full-text entities

- **Genes:** Slc6a3 (solute carrier family 6 (neurotransmitter transporter, dopamine), member 3) [NCBI Gene 13162] {aka DAT, Dat1}, OPN5 (opsin 5) [NCBI Gene 428670] {aka GPR136, GRP136, Opn5m, PGR12, TMEM13, cOpn5m}, Opn1sw (opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)) [NCBI Gene 12057] {aka Bcp}, Opn3 (opsin 3) [NCBI Gene 13603] {aka ERO, Ecpn}, OPN4 (opsin 4) [NCBI Gene 423609] {aka MOP, OPN4-2, OPN4m, cOpn4L, melanopsin, opsin-4}, Gria4 (glutamate receptor, ionotropic, AMPA4 (alpha 4)) [NCBI Gene 14802] {aka GluA4, GluR-D, Glur-4, Glur4, Gluralpha4, spkw1}, Dusp4 (dual specificity phosphatase 4) [NCBI Gene 319520] {aka 2700078F24Rik, E130306H24Rik, MKP2}, OPN5 (opsin 5) [NCBI Gene 221391] {aka GPR136, GRP136, PGR12, TMEM13}, Opn4 (opsin 4 (melanopsin)) [NCBI Gene 30044] {aka 1110007J02Rik, Gm533}, Opn1mw (opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan)) [NCBI Gene 14539] {aka Gcp, ML-opsin, Opn1lw, Rsvp}, Egr1 (early growth response 1) [NCBI Gene 13653] {aka A530045N19Rik, ETR103, Egr-1, Krox-1, Krox-24, Krox24}, OPN4 (opsin 4) [NCBI Gene 94233] {aka MOP}, Vsx2 (visual system homeobox 2) [NCBI Gene 12677] {aka Chx10, Hox-10, Hox10, or}, Bmal1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 11865] {aka Arnt3, Arntl, BMAL1b, MOP3, bHLHe5, bmal1b'}, Kdr (kinase insert domain protein receptor) [NCBI Gene 16542] {aka 6130401C07, Flk-1, Flk1, Krd-1, Ly73, VEGFR-2}, Opn5 (opsin 5) [NCBI Gene 353344] {aka Gpr136, Neuropsin, PGR12, TMEM13}, Gja1 (gap junction protein, alpha 1) [NCBI Gene 14609] {aka Cnx43, Cx43, Cx43alpha1, Cxnk1, Gja-1, Npm1}, Gnat2 (G protein subunit alpha transducin 2) [NCBI Gene 14686] {aka Gnat-2, Gt-2, Hg1d, Tcalpha}, Drd1 (dopamine receptor D1) [NCBI Gene 13488] {aka C030036C15Rik, Drd-1, Drd1a, Gpcr15}, OPN3 (opsin 3) [NCBI Gene 23596] {aka ECPN, PPP1R116}, Rho (rhodopsin) [NCBI Gene 212541] {aka Noerg1, Opn2, Ops, RP4}, RHO (rhodopsin) [NCBI Gene 751791] {aka CSNBAD1, OPN2, RDP1, RP4, opsin-2}, Kcnh2 (potassium voltage-gated channel, subfamily H (eag-related), member 2) [NCBI Gene 16511] {aka ERG1, LQT, Lqt2, M-erg, Merg1, merg1a}, Ccn2 (cellular communication network factor 2) [NCBI Gene 14219] {aka Ctgf, Fisp12, Hcs24, fisp-12}, OPN1LW [NCBI Gene 20164]
- **Diseases:** visual blur (MESH:D014786), myopic macular degeneration (MESH:D008268), AL (MESH:D009101), myopic (MESH:D001251), choroidal thinning (MESH:D013851), asthma (MESH:D001249), refractive error (MESH:D012030), LIM (MESH:D007905), depression (MESH:D003866), Myopia (MESH:D009216), axial elongation (MESH:C537791), ischemia (MESH:D007511), glaucoma (MESH:D005901), hypoxia (MESH:D000860), retinopathy of prematurity (MESH:D012178), hyperopia (MESH:D006956), LLRL (MESH:D009800), skin lesions (MESH:D012871), form deprivation myopia (MESH:D012892), blindness (MESH:D001766), optic neuropathy (MESH:D009901)
- **Chemicals:** Dopamine (MESH:D004298), L-DOPA (MESH:D007980), LLRL (-), 3,4-dihydroxyphenylacetic acid (MESH:D015102), Crocetin (MESH:C487773), atropine (MESH:D001285), oxygen (MESH:D010100), AL (MESH:D000535), DTA (MESH:C042899)
- **Species:** Cavia porcellus (domestic guinea pig, species) [taxon 10141], Gardenia jasminoides (species) [taxon 114476], Xenopus laevis (African clawed frog, species) [taxon 8355], Gallus gallus (bantam, species) [taxon 9031], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Macaca mulatta (rhesus macaque, species) [taxon 9544], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986]
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU)

## Full text

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Source: https://tomesphere.com/paper/PMC12861076