Regulation of reduced-folate transporter-1 in retinal pigment epithelial cells by folate

Purpose: Reduced-folate transporter-1 (RFT-1), a typical transport protein with 12 membrane-spanning domains, transports reduced-folates, such as N-5-methyltetrahydrofolate (MTF), the predominant circulating form of folate. RFT-1 is localized to the RPE apical membrane and transports folate from RPE to photoreceptor cells. We asked whether RFT-1 activity in RPE is altered under high folate conditions. Materials and methods: ARPE-19 cells were cultured 24,48, or 72 h in medium containing either 0.5 nM, 5.0 nM, or 2.26 muM MTF, and the activity of RFT-1 was assessed by determining the uptake of N-5-MTF. Semi quantitative reverse transcription-polymerase chain reaction and Western blot analysis were used to study RFT-1 gene and protein expression. Results: Cells treated for 72 h with 2.26 muM MTF showed a significant (40%) decrease in MTF uptake compared to cells exposed to 0.5 nM or 5 nM MTE The effect of high concentrations of folate on RFT-1 activity was specific. Kinetic analysis showed that folate-mcluced attenuation of RFT-1 activity was associated with a decrease in the maximal velocity of the transporter, but no change in the substrate affinity. Steady-state levels of RFT-1 mRNA and protein decreased significantly in the presence of excess folate. Conclusions: Excess folate levels downregulate RFT-1 in RPE. This study represents the first molecular analysis of the regulation of RFT-1 by folate in RPE and reveals attenuation of the activity and expression of a folate transport protein under conditions of high levels of folate.