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Uptake and esterification of vitamin A by RCS rat retinal pigment epithelial cells in primary culture.

Authors: Cia, D  Bonhomme, B  Azais-Braesco, V  Cluzel, J  Doly, M 
Citation: Cia D, etal., Vision Res. 2004 Feb;44(3):247-55.
Pubmed: (View Article at PubMed) PMID:14642897

We investigated the capacity of Royal College of Surgeons (RCS) rat retinal pigment epithelial (RPE) cells to take up all-trans-retinol (ROL) (vitamin A) and to metabolize it into retinyl esters (RE). Cultures of RPE cells were established from RCS and control newborn rats. All-trans-ROL was delivered to the apical surface of the RPE monolayer. Retinoids were analyzed by high-performance liquid chromatography. The cellular retinol-binding protein type I (CRBP-I) was assessed by Western blotting. Before supplementation with ROL, RE were lower in RCS rats. After ROL supplementation, esters increased and reached values that were similar in the two strains, but the increase, expressed relative to the initial value, was higher in RCS rats. The uptake of ROL and the level of CRBP-I were greater in RCS rats. Our results provide evidence of a functional retinol esterifying enzyme in cultured RCS RPE cells and suggest that CRBP-I could play a role in the uptake and esterification of ROL in the RPE cells.

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CRRD Object Information
CRRD ID: 6484737
Created: 2012-07-03
Species: All species
Last Modified: 2012-07-03
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.