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Peer-reviewedCC BY-NC-NDInvestigative ophthalmology & visual science

S-Opsin Contributes to Violet Light-Dependent Refractive Development and Is Associated With Corneal Structural Remodeling in Mice.

4 affiliations
  1. 1Department of Ophthalmology, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
  2. 2Department of Ophthalmology, Fujian Children's Hospital (Fujian Branch of Shanghai Children's Medical Center), College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
  3. 3Shanghai Eye Diseases Prevention & Treatment Center, School of Medicine, Tongji University, Shanghai, China.
  4. 4College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.

Abstract

Purpose

To determine whether S-opsin is involved in the refractive response to violet light (VL) in mice and whether loss of Opn1sw is accompanied by corneal structural and biomechanical changes.Methods

Wild-type (WT) and Opn1sw-/- mice were exposed to VL or white light (WL) from 4 to 8 weeks of age. Refractive error, axial length, corneal curvature, and the ratio of axial length to corneal radius (AL/CR) were measured. Retinal morphology and opsin expression were assessed by histological and molecular analyses, and retinal function was evaluated by electroretinography. Corneal biomechanics and extracellular matrix composition were evaluated by atomic force microscopy and molecular analyses.Results

VL induced a hyperopic shift in WT mice compared with WL (11.83 ± 1.13 D vs. 9.25 ± 0.82 D; P < 0.01) and reduced the AL/CR ratio (2.075 ± 0.030 vs. 2.140 ± 0.021; P < 0.01), without significant changes in AL or CR. At baseline, Opn1sw-/- mice were more myopic than WT littermates (7.00 ± 1.27 D vs. 11.08 ± 0.80 D; P < 0.0001), with a smaller CR (1.395 ± 0.044 mm vs. 1.454 ± 0.021 mm; P < 0.05) and a higher AL/CR ratio (2.240 ± 0.032 vs. 2.156 ± 0.021; P < 0.001). After light exposure, Opn1sw-/- mice failed to exhibit the VL-induced hyperopic response observed in WT mice. Opn1sw deficiency was also associated with reduced photopic electroretinogram (ERG) responses, modest outer nuclear layer thinning, reduced corneal stiffness, and decreased corneal COL4A1 expression.Conclusions

S-opsin contributes to the refractive response to VL in mice. Loss of Opn1sw is associated with altered corneal curvature, reduced corneal stiffness, and extracellular matrix remodeling in the absence of axial elongation.

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BibTeX
@article{huang2026sopsin,
  title = {{S-Opsin Contributes to Violet Light-Dependent Refractive Development and Is Associated With Corneal Structural Remodeling in Mice.}},
  author = {Jinfang Huang and Yining Shen and Rui Duan and Yuanyang Huang and Cheng Fang and Huiling Shen and Leilei Zou and Hong Liu},
  journal = {Investigative ophthalmology \& visual science},
  year = {2026},
  month = oct,
  doi = {10.1167/iovs.67.12.19},
  url = {https://europepmc.org/article/MED/42853008},
  note = {CC BY-NC-ND},
}
RIS
TY  - JOUR
TI  - S-Opsin Contributes to Violet Light-Dependent Refractive Development and Is Associated With Corneal Structural Remodeling in Mice.
AU  - Jinfang Huang
AU  - Yining Shen
AU  - Rui Duan
AU  - Yuanyang Huang
AU  - Cheng Fang
AU  - Huiling Shen
AU  - Leilei Zou
AU  - Hong Liu
PY  - 2026
DA  - 2026/10/01
JO  - Investigative ophthalmology & visual science
DO  - 10.1167/iovs.67.12.19
UR  - https://europepmc.org/article/MED/42853008
AB  - Purpose  To determine whether S-opsin is involved in the refractive response to violet light (VL) in mice and whether loss of Opn1sw is accompanied by corneal structural and biomechanical changes.Methods  Wild-type (WT) and Opn1sw-/- mice were exposed to VL or white light (WL) from 4 to 8 weeks of age. Refractive error, axial length, corneal curvature, and the ratio of axial length to corneal radius (AL/CR) were measured. Retinal morphology and opsin expression were assessed by histological and molecular analyses, and retinal function was evaluated by electroretinography. Corneal biomechanics and extracellular matrix composition were evaluated by atomic force microscopy and molecular analyses.Results  VL induced a hyperopic shift in WT mice compared with WL (11.83 ± 1.13 D vs. 9.25 ± 0.82 D; P < 0.01) and reduced the AL/CR ratio (2.075 ± 0.030 vs. 2.140 ± 0.021; P < 0.01), without significant changes in AL or CR. At baseline, Opn1sw-/- mice were more myopic than WT littermates (7.00 ± 1.27 D vs. 11.08 ± 0.80 D; P < 0.0001), with a smaller CR (1.395 ± 0.044 mm vs. 1.454 ± 0.021 mm; P < 0.05) and a higher AL/CR ratio (2.240 ± 0.032 vs. 2.156 ± 0.021; P < 0.001). After light exposure, Opn1sw-/- mice failed to exhibit the VL-induced hyperopic response observed in WT mice. Opn1sw deficiency was also associated with reduced photopic electroretinogram (ERG) responses, modest outer nuclear layer thinning, reduced corneal stiffness, and decreased corneal COL4A1 expression.Conclusions  S-opsin contributes to the refractive response to VL in mice. Loss of Opn1sw is associated with altered corneal curvature, reduced corneal stiffness, and extracellular matrix remodeling in the absence of axial elongation.
SN  - 0146-0404
SN  - 1552-5783
ER  -