Retinoic acid regulates foveal development in the human retina

The fovea is a region of the human retina specialized for high-acuity vision, with a high density of cones and no rod photoreceptors. Recent studies using retinal organoids indicate that retinoic acid (RA) may play a key role in foveal development: low RA levels in the fovea, maintained by CYP26A1, lead to early cell cycle exit for progenitors and a low rod-to-cone ratio. To test this model in fetal human development, we studied human fetal retina in 3D cultures in the presence of RA and RA inhibitors. We find that inhibition of RA reduces retinal progenitor proliferation and rod development, while a high concentration of RA promotes rod fate and represses cone opsin expression. Moreover, inhibition of RA signaling promotes expression of M/L-opsins over S-opsin, a feature of the fovea. Our results demonstrate that RA levels control several key features of foveal development in human fetal retina.

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Publication Details

Journal
Cell Reports
Published
2026-05-29
DOI
https://doi.org/10.1016/j.celrep.2026.117379
Primary Topic
Retinoids in leukemia and cellular processes
Type
article
Field-Weighted Citation Impact
0.00

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article

Retinoic acid regulates foveal development in the human retina

Joshua Hahn, Juliette Wohlschlegel, Lew Kaplan, Kayla L. Arakelian et al.
Cell Reports
Retinoids in leukemia and cellular processes
article

Retinoic acid regulates foveal development in the human retina

Joshua Hahn, Juliette Wohlschlegel, Lew Kaplan, Kayla L. Arakelian, Abigail L. Green, Guy Federle, Ian A. Glass, Aric Prieve, Lydia R. Lee, Thomas A. Reh
article en

Abstract

The fovea is a region of the human retina specialized for high-acuity vision, with a high density of cones and no rod photoreceptors. Recent studies using retinal organoids indicate that retinoic acid (RA) may play a key role in foveal development: low RA levels in the fovea, maintained by CYP26A1, lead to early cell cycle exit for progenitors and a low rod-to-cone ratio. To test this model in fetal human development, we studied human fetal retina in 3D cultures in the presence of RA and RA inhibitors. We find that inhibition of RA reduces retinal progenitor proliferation and rod development, while a high concentration of RA promotes rod fate and represses cone opsin expression. Moreover, inhibition of RA signaling promotes expression of M/L-opsins over S-opsin, a feature of the fovea. Our results demonstrate that RA levels control several key features of foveal development in human fetal retina.

Cell ReportsVol. 45(6)
California Institute for Regenerative Medicine (US), University of Washington (US), Institute for Stem Cell Biology and Regenerative Medicine (IN), Seattle Children's Hospital (US)
Foundation Fighting Blindness, BrightFocus Foundation
Zero hunger
Openalex Percentile: Top 9%
Retinoids in leukemia and cellular processes
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