| First Author | Radhakrishnan R | Year | 2025 |
| Journal | FASEB Bioadv | Volume | 7 |
| Issue | 8 | Pages | e70044 |
| PubMed ID | 40909872 | Mgi Jnum | J:386300 |
| Mgi Id | MGI:8346460 | Doi | 10.1096/fba.2025-00173 |
| Citation | Radhakrishnan R, et al. (2025) Rescue of the Stargardt Disease Phenotype in Abca4 Knockout Mice Through Dietary Modulation of the Vitamin A Receptor RBPR2. FASEB Bioadv 7(8):e70044 |
| abstractText | Mutations in the ABCA4 gene in Stargardt disease (STGD1) cause enhanced accumulation of cytotoxic lipofuscin, manifesting in RPE atrophy and photoreceptor dysfunction. One component of lipofuscin is the all-trans-retinal derivative, pyridinium bisretinoid A2E. Since ocular A2E biosynthesis relies on all-trans-retinal, which is obtained from circulating all-trans-retinol bound to retinol binding protein 4 (RBP4-ROL), we hypothesized that modulating vitamin A receptors, such as RBPR2, which regulate serum RBP4-ROL homeostasis, should in principle attenuate A2E production. In silico analysis revealed multiple retinoic acid response element (RARE) binding sites on the murine Rbpr2 gene promoter, which was confirmed in vitro by EMSA and ChIP assays. In vitro luciferase assays showed that Rbpr2 promoter activity was induced by exogenous beta-carotene (BC) metabolites. Dietary BC supplementation of Abca4 (-/-) mice, a mouse model for STGD1, increased hepatic all-trans-retinoic acid and 9-cis-retinoic acid production, which induced Rbpr2 mRNA expression. This mechanism decreased serum RBP4 protein levels, fundus lipofuscin autofluorescence, and ocular A2E accumulation, altogether improving photoreceptor and RPE function. Conversely, such a rescue was not observed in either Abca4 (-/-) mice fed a diet devoid of BC or in double knockout Rbpr2 (-/-); Abca4 (-/-) mice. Thus, there was a significant inverse correlation between dietary BC supplementation and Rbpr2 gene presence in Abca4 (-/-) mice, to that of lipofuscin accumulation in Abca4 (-/-) mice on diets devoid of BC or in Rbpr2 (-/-); Abca4 (-/-) mice. Our results provide impetus to include dietary obtained BC for STGD1 patients with ABCA4 gene mutations and identify a novel role for the vitamin A receptor RBPR2 in this process. |
