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Inhibition of the Na⁺/Dicarboxylate Cotransporter by Anthranilic Acid Derivatives

Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, Texas

Received February 20, 2007; accepted August 22, 2007

	Abstract

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The Na⁺/dicarboxylate cotransporter NaDC1 absorbs citric acid cycle intermediates from the lumen of the small intestine and kidney proximal tubule. No effective inhibitor has been identified yet, although previous studies showed that the nonsteroidal anti-inflammatory drug, flufenamate, inhibits the human (h) NaDC1 with an IC₅₀ value of 2 mM. In the present study, we have tested compounds related in structure to flufenamate, all anthranilic acid derivatives, as potential inhibitors of hNaDC1. We found that N-(p-amylcinnamoyl) anthranilic acid (ACA) and 2-(p-amylcinnamoyl) amino-4-chloro benzoic acid (ONO-RS-082) are the most potent inhibitors with IC₅₀ values lower than 15 µM, followed by N-(9-fluorenylmethoxycarbonyl)-anthranilic acid (Fmoc-anthranilic acid) with an IC₅₀ value of 80 µM. The effects of ACA on NaDC1 are not mediated through a change in transporter protein abundance on the plasma membrane and seem to be independent of its effect on phospholipase A₂ activity. ACA acts as a slow inhibitor of NaDC1, with slow onset and slow reversibility. Both uptake activity and efflux are inhibited by ACA. Other Na⁺/dicarboxylate transporters from the SLC13 family, including hNaDC3 and rbNaDC1, were also inhibited by ACA, ONO-RS-082, and Fmoc-anthranilic acid, whereas the Na⁺/citrate transporter (hNaCT) is much less sensitive to these compounds. The endogenous sodium-dependent succinate transport in Caco-2 cells is also inhibited by ACA. In conclusion, ACA and ONO-RS-082 represent promising lead compounds for the development of specific inhibitors of the Na⁺/dicarboxylate cotransporters.

To date, no high-affinity inhibitors have been identified for any member of the SLC13 family. Our previous studies identified the nonsteroidal anti-inflammatory drug flufenamate as an inhibitor of hNaDC1. The IC₅₀ value was 2 mM using succinate as a substrate and 0.5 mM using methylsuccinate (Pajor and Sun, 1996; Smith et al., 2003). A high-affinity inhibitor would be very useful for in vitro studies of NaDC1 to quantitate the transporter in the membrane and to characterize mutant transporters with alterations in substrate translocation but not binding. An effective and selective inhibitor could help to identify physiological roles of NaDC1. Furthermore, an inhibitor may lead to a potential drug if inhibition of NaDC1 activity in humans is linked to aging or metabolism.

In the present study, we tested anthranilic acid derivatives related in structure to flufenamate as potential inhibitors of hNaDC1. We found that N-(p-amylcinnamoyl) anthranilic acid (ACA) and 2-(p-amylcinnamoyl) amino-4-chloro benzoic acid (ONO-RS-082) are the most potent inhibitors with IC₅₀ values lower than 15 µM, followed by N-(9-fluorenylmethoxycarbonyl)-anthranilic acid (Fmoc-anthranilic acid) with an IC₅₀ value of 80 µM. The effects of ACA on hNaDC1 are not mediated through a change in transporter protein abundance on the plasma membrane and seem to be independent of its effect on phospholipase A₂ (PLA₂) activity. ACA acts as a slow inhibitor of NaDC1, with slow onset and slow reversibility. Both transport uptake and efflux are inhibited by ACA. Other Na⁺/dicarboxylate transporters from the SLC13 family, including hNaDC3 and rbNaDC1, were also inhibited by ACA, ONO-RS-082, and Fmoc-anthranilic acid, whereas the Na⁺/citrate transporter hNaCT is much less sensitive to these compounds. The endogenous sodium-dependent succinate transport activity in the human colon carcinoma cell line, Caco-2, is also sensitive to inhibition by ACA. In conclusion, ACA and ONO-RS-082 are promising lead compounds for the development of specific inhibitors of the Na⁺/dicarboxylate cotransporters.

	Materials and Methods

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Chemicals. The structures of the compounds used in this study are shown in Fig. 1, and the names are listed in Table 1. ACA, ONO-RS-082, and Tranilast were purchased from BIOMOL Research Laboratories (Plymouth Meeting, PA), and all other chemicals were from Sigma-Aldrich (St. Louis, MO).

View larger version (10K): [in this window] [in a new window]   Fig. 1. Structures of the compounds used in this study. The names of the compounds are listed in Table 1.

Cell Culture. The CUBS cell line consisting of HRPE cells (derived from human retinal pigment epithelium) stably transfected with the human NaDC1 cDNA (Smith et al., 2003) was a generous gift from Dr. Chari Smith (GlaxoSmithKline, Research Triangle Park, NC). Control cells were nontransfected HRPE cells. Cells were cultured in modified Eagle's medium containing Earle's salts, GlutaMAX I, and 25 mM HEPES (Invitrogen, Carlsbad, CA) supplemented with 10% heat-inactivated fetal calf serum (Hyclone, Logan, UT), 100 U/ml penicillin, 100 µg/ml streptomycin, and 700 µg/ml G-418 (Geneticin; Invitrogen) at 37°C in 5% CO₂. For uptake experiments, cells were plated on white-sided 24-well plastic Visiplates (PerkinElmer Life and Analytical Sciences, Waltham, MA) at a density of 2.5 x 10⁵ cells/well (24-well plate) in the same medium with 2.5 mM butyrate added. Control HRPE cells were plated at the same density but without G418 or butyrate in the medium. Uptake assays were done in confluent monolayers approximately 36 h after plating.

For transient transfections with hNaDC3 and hNaCT, HRPE cells were plated at 1.2 x 10⁵ cells/well, and each well of cells was transfected with 1.8 µl of FuGENE 6 (Roche, Indianapolis, IN) and 0.6 µg of plasmid DNA (9:3 ratio) (Pajor and Randolph, 2005). Transport assays were done 48 h after transfections.

Succinate Uptake Assay. Transport assays at room temperature were as described previously (Pajor and Randolph, 2005). The sodium buffer contained 120 mM NaCl, 5 mM KCl, 1.2 mM MgCl₂, 1.2 mM CaCl₂, 5 mM D-glucose, and 25 mM HEPES, with pH adjusted to 7.4 with 1 M Tris. Choline buffer contained 120 mM choline chloride in place of NaCl. For the assays, each well was washed twice with 1 ml of sodium buffer and then preincubated with inhibitor in sodium buffer for 15 min, followed by two washes with 1 ml each of sodium buffer. Inhibitors were prepared fresh each day as dimethyl sulfoxide stocks, with a final volume of dimethyl sulfoxide of less than 1%. Cells were preincubated with inhibitors 15 min (unless otherwise specified in the figure legends). Transport solution (0.25 ml/well) consisting of [¹⁴C]succinate (10 or 100 µM final concentration) in sodium buffer, with or without added inhibitor, was then added to the cells. After 30 min, the uptake measurements were stopped, and radioactivity was removed with four 1-ml washes of choline buffer. After the last wash was removed, each well of cells was dissolved in 0.5 ml of scintillation cocktail, OptiPhase Supermix (PerkinElmer Life and Analytical Sciences). The plates were sealed with plastic plate covers and were counted directly in a Microbeta Trilux 1450 plate scintillation counter (PerkinElmer Life and Analytical Sciences). For experiments involving CUBS cells, background corrections were made based on uptake activities in control HRPE cells. For experiments involving transfected cells, uptake activities in vector-transfected cells were subtracted from activities in NaDC plasmid-transfected cells. There was no difference in the background counts obtained with vector-transfected or nontransfected cells (results not shown).

For the calculation of K_i values from Dixon plots, inhibition of transport activity was measured at multiple inhibitor and substrate concentrations. The data were analyzed by linear regression, and the x-axis value corresponding to the intersection of the lines was taken as –K_i (Segel, 1975). To determine IC₅₀ values (the inhibitor concentration resulting in 50% inhibition), the transport of 10 µM[¹⁴C]succinate was measured in the presence of increasing concentrations of inhibitor, and the resulting activity (v%, as a percentage of control) was analyzed by nonlinear regression using v% = IC₅₀/([I] + IC₅₀) x 100, where [I] represents the inhibitor concentration. Statistical analysis with one-way analysis of variance or Student's t test was done using the SigmaStat program (Systat Software, Inc., Point Richmond, CA). Each experimental point was the mean of four replicate wells, and each experiment was repeated at least two or three times (different plating or transfection experiments).

Efflux Assays. Efflux assays in CUBS cells (Smith et al., 2003) were done using the nonmetabolizable substrate, [³H]methylsuccinate (a gift of Dr. Chari Smith, GlaxoSmithKline). In preliminary experiments (data not shown), we found that the cells required at least 30 min of incubation with substrate for preloading, after which the intracellular radioactivity reached a plateau. Therefore, the cells were preloaded by incubating with 10 or 100 µM[³H]methylsuccinate in Na⁺ buffer for 30 min. The cells were then washed four times with choline buffer to remove extracellular radioactivity, followed by incubation in sodium buffer for 1 min to allow efflux of radiolabeled substrate. To stop the efflux, each well was washed four times with choline buffer, and 1% SDS was added to solubilize the cells. The samples were transferred to scintillation vials (because the plate counter does not measure ³H accurately), combined with scintillation cocktail, and counted on a Packard Tri-Carb 2100TR scintillation counter (PerkinElmer Life and Analytical Sciences).

Caco-2 Cells. The Caco-2 cell line (human colon adenocarcinoma) was obtained from the American Type Culture Collection (Manassas, VA). The cells were cultured in DMEM with 4.5 g/l glucose (Invitrogen) supplemented with 10% heat-inactivated fetal calf serum (Hyclone), 100 U/ml penicillin G, 100 µg/ml streptomycin, 1% (v/v) sodium pyruvate, and 1% (v/v) nonessential amino acids (Sigma). Cells were seeded in 24-well collagen-coated plates, maintained with medium changes every other day, and then used for transport assays 21 days after reaching confluence. Sodium-dependent transport activity was the difference between transport measured in sodium and choline-containing buffers.

Cell Surface Biotinylation. Cell surface biotinylations of NaDC1 were done using a membrane-impermeant reagent, sulfosuccinimidyl-6-(biotinamido) hexanoate (Sulfo-NHS-LC-Biotin; Pierce, Rockford, IL), as described previously (Pajor and Randolph, 2005). Biotinylated proteins were separated by SDS-polyacrylamide gel electrophoresis in 7.5% acrylamide, and NaDC1 was identified using antibodies (1:1000 dilution).

	Results

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Initial Inhibitor Screen. The time course of [¹⁴C]succinate uptake into the CUBS cell line (stably transfected HRPE cells expressing hNaDC1) is linear through 45 min (Fig. 2). Therefore, 30-min uptake activities were used in subsequent experiments as estimates of initial rates. Succinate uptake activity in control nontransfected HRPE cells was very low (Fig. 2). The transport of succinate in choline buffer in the CUBS cell line was the same as in nontransfected HRPE cells (results not shown).

View larger version (11K): [in this window] [in a new window]   Fig. 2. Time course of [14C]succinate transport (10 µM) in the CUBS cell line (HRPE cells stably expressing hNaDC1) compared with control HRPE cells. Each point represents the mean ± range of two wells from a single representative experiment.

View larger version (19K): [in this window] [in a new window]   Fig. 3. Inhibition of 10 µM[14C]succinate transport by anthranilic acid derivatives in hNaDC1 expressed in CUBS cells. The numbers refer to different compounds as described in Table 1 and Fig. 1. The test inhibitor concentration was 100 µM. Thirty-minute uptake measurements were done, and the data are expressed as a percentage of control in the absence of inhibitor. The data points represent mean ± range or S.E.M., n = 2 to 3 experiments. *, significant difference from control, p < 0.05.

View larger version (13K): [in this window] [in a new window]   Fig. 4. Dixon plots of ACA inhibition of hNaDC1 in the CUBS cell line. Transport assays were done in 24-well plates at two different [14C]succinate concentrations (10 and 100 µM) and increasing amounts of ACA. The data points represent mean ± S.E.M., n = 4 wells, from a single representative experiment. The Ki value in this experiment is 12.5 µM.

View larger version (63K): [in this window] [in a new window]   Fig. 5. Western blot of cell surface biotinylated hNaDC1 in the CUBS cell line. Cells were incubated with sodium buffer with or without 25 µM ACA for 20 min. The cell surface proteins were labeled with the membrane-impermeant reagent Sulfo-NHS-LC-Biotin, as described under Materials and Methods. Western blots of biotinylated proteins were probed with anti-NaDC1 antibodies (1:1000 dilution) followed by horseradish peroxidase-linked anti-rabbit immunoglobulin (1:5000 dilution). The chemiluminescent size standards (Magic Mark) are shown in lane 1.

View larger version (11K): [in this window] [in a new window]   Fig. 6. Time course of inhibition by ACA. Transport of 10 µM[14C]succinate by hNaDC1 in the CUBS cell line was measured in the absence (control) or presence (+ACA) of 50 µM ACA. Data points represent means ± range of duplicate measurements; some error bars are smaller than the points.

View larger version (9K): [in this window] [in a new window]   Fig. 7. Time courses of ACA preincubation and postincubation with hNaDC1 in the CUBS cell line. A, onset, the cells were preincubated with or without 50 µM ACA in sodium buffer for up to 30 min, and then transport of [14C]succinate was assayed for 30 min. Data are expressed as a percentage of control at each time point (parallel incubation in the absence of ACA). B, reversibility, the cells were incubated with 30 µM ACA for 15 min, and the ACA was washed away, and the cells were then incubated in sodium buffer for up to 60 min. Control cells were incubated with sodium buffer only. Transport of 10 µM [14C]succinate was measured for 30 min. Data shown are means ± S.E.M., n = 4 wells.

Efflux Experiments. We next tested the efflux of the nonmetabolizable substrate [³H]methylsuccinate in the CUBS cell line. The cells were preloaded with radiolabeled substrate in sodium buffer for 30 min. The extracellular radioactivity was washed away, and the efflux was measured for 1 min in sodium buffer with or without 100 µM ACA. As shown in Fig. 8, approximately 40 to 50% of the [³H]methylsuccinate remained in the cells after 1 min compared with controls at time 0. The addition of 100 µM ACA resulted in an increased retention of [³H]methylsuccinate during the efflux period (Fig. 8), indicating that efflux and influx are inhibited by ACA.

View larger version (13K): [in this window] [in a new window]   Fig. 8. Effect of ACA on efflux. CUBS cells expressing hNaDC1 were preloaded by incubating with [3H]methylsuccinate (10 or 100 µM) for 30 min. The extracellular radioactivity was washed away, and the cells were then incubated with sodium buffer alone (control) or with 100 µM ACA (+ACA) for 1 min. The data shown are the means ± S.E.M., n = 4 experiments. *, significantly different from control group, p < 0.05.

Phospholipase A₂ Inhibitors. Because ACA is known to be a nonspecific inhibitor of PLA₂ (Konrad et al., 1992), we wanted to rule out the possibility that the effects of ACA on NaDC1 are mediated indirectly by inhibition of PLA₂. Two other inhibitors of PLA₂, structurally unrelated to ACA, were tested, but they did not inhibit succinate transport by hNaDC1 (Fig. 9). p-Bromophenacyl bromide (BPB) inhibits secreted PLA₂ by binding covalently to a histidine residue (Mayer and Marshall, 1993). A previous study showed that BPB at 5 or 10 µM inhibits PLA₂ activity in cultured cells without producing toxicity (Liu and Levy, 1997). AACOCF₃ (arachidonyl trifluoromethyl ketone) is a slow-onset inhibitor of the calcium-dependent cytosolic PLA₂ (Street et al., 1993). Both compounds were tested after 15 min of preincubation. The results suggest that the effects of ACA on hNaDC1 are distinct from its inhibition of PLA₂.

View larger version (12K): [in this window] [in a new window]   Fig. 9. Effect of phospholipase A2 inhibitors on [14C]succinate transport by hNaDC1 in CUBS cells. The inhibitors BPB and AACOCF3 were applied at 10 µM for a 15-min preincubation followed by coincubation with [14C]succinate during the 30-min uptake period. Control cells were incubated in sodium buffer without inhibitor. Data are means ± range of duplicate experiments.

View larger version (19K): [in this window] [in a new window]   Fig. 10. Sensitivity of the high-affinity Na+/dicarboxylate cotransporter, hNaDC3, the Na+/citrate cotransporter, hNaCT, and the low-affinity Na+/dicarboxylate cotransporter, rbNaDC1 to inhibition by anthranilic acid derivatives. Compound names are listed in Table 1, and structures are shown in Fig. 1. HRPE cells were transiently transfected with plasmids containing transporter cDNA, control cells were transfected with the pcDNA3.1 vector plasmid. Transport of 10 µM [14C]succinate (hNaDC3, rbNaDC1) or [14C]citrate (hNaCT) was measured for 30 min in the presence or absence of 100 µM inhibitor. Data shown are means ± range or S.E.M., n = 2 to 3 experiments, except for rbNaDC1 with compound 11 (n = 1).

Inhibition of Endogenous Transporter. The human colon carcinoma cell line, Caco-2, is often used as a model of the small intestine. This cell line expresses sodium-dependent transport of succinate that is predominantly mediated by NaDC1 with some contribution by NaCT (Weerachayaphorn and Pajor, 2005). As shown in Fig. 11, the endogenous succinate transport activity in Caco-2 cells was inhibited more than 50% by treatment with ACA. Therefore, ACA inhibits both transfected recombinant NaDC1 and the endogenous NaDC1 found in Caco-2 cells.

View larger version (9K): [in this window] [in a new window]   Fig. 11. Endogenous sodium-dependent succinate transport in Caco-2 cells treated with or without 50 µM ACA. Caco-2 cell monolayers were grown 21 days after reaching confluence. The cells were preincubated for 15 min with ACA or sodium buffer alone and then transport of 100 µM [14C]succinate was measured in sodium or choline buffer for 30 min. Data shown are means ± S.E.M., n = 3 experiments. *, significant difference from control, p < 0.05.

	Discussion

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Flufenamate was identified in previous studies as a low-affinity inhibitor of both low-affinity (NaDC1) and high-affinity (NaDC3) Na⁺/dicarboxylate cotransporters. There are species differences in sensitivity to flufenamate, with rbNaDC1 being most sensitive, having an IC₅₀ value of 250 µM (Pajor and Sun, 1996), followed by flounder NaDC3, with an IC₅₀ value of 1 mM (Burckhardt et al., 2004), and hNaDC1, with an IC₅₀ value of 2 mM (Pajor and Sun, 1996). All of the experiments were done using X. laevis oocytes as an expression system, and the cells were not preincubated with inhibitor. In the present study, the IC₅₀ value for flufenamate in rbNaDC1 was 100 µM, and the cells were preincubated with inhibitor before the assay, which may account for the apparent difference in affinity. Inhibition of the flounder NaDC3 by flufenamate seems to be mediated, at least in part, by an increased K⁺ conductance that is associated with the transporter, because it was not seen in control oocytes (Burckhardt et al., 2004). It is possible that flufenamate activates a channel activity of the fNaDC3 protein, and several members of the SLC13 family have both channel and transport activity (Oshiro and Pajor, 2005).

The onset of inhibition of hNaDC1 by ACA was not evident until after at least 2-min incubation time, consistent with the properties of a slow-binding inhibitor. This is the first report that ACA behaves as a slow-binding inhibitor. Slow-binding inhibitors are reversible, competitive inhibitors, but the rate of reaching equilibrium is slow relative to a classic inhibitor (Morrison, 1982). Slow inhibition may occur if the formation of the enzyme-inhibitor complex occurs more slowly than the production of reaction product (in the case of a transporter, the "product" of the reaction is the appearance of substrate on the inside of the cell). Alternatively, the enzyme and inhibitor complex forms quickly, but there is a slow isomerization step to an inactive complex. Slow inhibitors tend to be useful drugs because of their slow reversibility and the gradual accumulation of the inactive enzyme-inhibitor complex. Examples of drugs that are slow inhibitors include nonsteroidal anti-inflammatory drugs, such as indomethacin, that inhibit prostaglandin H synthase I by slow, reversible isomerization to a second enzyme-inhibitor complex (Callan et al., 1996). The arachidonic acid analog AACOCF₃ is a slow and tight-binding inhibitor of the cytosolic phospholipase A₂ (Street et al., 1993).

Our current working hypothesis for the effects of the inhibitors identified in the present study is that they act directly on hNaDC1 to inhibit transport. Other hypotheses could also explain the results, but they can be ruled out. For example, ACA could inhibit transport by affecting protein targeting. Both ACA (IC₅₀ = 8 µM) and ONO-RS-082 (IC₅₀ = 6 µM) have been shown to disrupt Golgi trafficking (de Figueiredo et al., 1999). However, the cell surface abundance of hNaDC1 was not affected by incubation with ACA. A second possible explanation is that ACA inhibits transport indirectly by affecting the membrane potential or Na⁺ chemical gradient, which would affect hNaDC1 because it is electrogenic (Yao and Pajor, 2000). ONO-RS-082 has been shown to inhibit the H⁺/K⁺-ATPase in stomach with an IC₅₀ value of 3.5 µM, and the same study also reported that ONO-RS-082 has a protonophore effect (Sugita et al., 2005). ACA is known to directly inhibit transient receptor potential cation channels with an IC₅₀ value of less than 4 µM (Kraft et al., 2006). However, changes in membrane potential or cation concentrations would not explain the time delay in the inhibition of hNaDC1 by ACA or the different sensitivities of NaDC1 homologs, all of which are electrogenic.

The hypothesis that ACA inhibition is mediated indirectly through its inhibition of PLA₂ is less likely than a direct effect of ACA on hNaDC1. There was no inhibition of hNaDC1 activity by two structurally unrelated PLA₂ inhibitors, BPB and AACOCF₃. A compound that has not been reported to have PLA₂ inhibitory activity, Fmoc-anthranilic acid (compound 4), also inhibited transport with an IC₅₀ value of approximately 80 µM. Although flufenamate has been shown to inhibit PLA₂ (Franson et al., 1980), only the rabbit and not the human NaDC1 was inhibited by flufenamate. Furthermore, meclofenamate (compound 11) is also a PLA₂ inhibitor with an IC₅₀ value of 1 µM at 1 mM Ca²⁺ (Franson et al., 1980), yet it had no effect on any of the transporters in this study.

In conclusion, we have identified several inhibitors of the Na⁺/dicarboxylate cotransporters with micromolar affinities that represent the highest-affinity inhibitors of the SLC13 family to date. The most potent inhibitors of hNaDC1 were ACA, ONO-RS-082, and Fmoc-anthranilic acid. There were some differences in sensitivity to inhibition by anthranilic acid derivatives among the NaDC1 homologs tested (hNaDC3, rbNaDC1, and hNaCT), although the selectivity of the compounds was relatively low. The endogenous sodium-dependent succinate transport activity in the human colon carcinoma cell line, Caco-2, is also sensitive to inhibition by ACA. The kinetics of ACA inhibition of hNaDC1 were consistent with slow inhibition, and both uptake and efflux were affected. Our data indicate that ACA inhibits the activity of hNaDC1 independently of PLA₂ inhibition. However, the lack of specificity of ACA and ONO-RS-082 with NaDC orthologs and the effects on other targets including PLA₂, transient receptor potential cation channels (Kraft et al., 2006), and the stomach H⁺/K⁺-ATPase (Sugita et al., 2005) would limit the use of these compounds as NaDC1 inhibitors. Therefore, the structures of the anthranilic acid derivatives will serve as a starting point in drug design targeting hNaDC1.

	Acknowledgements

 
We thank Dr. Chari D. Smith, of GlaxoSmithKline, for the generous donation of the CUBS cell line and [³H]methylsuccinate and for many helpful discussions. We also thank Jittima Weerachayaphorn for advice on Caco-2 cell cultures and transport assays.

	Footnotes

 
This work was supported by National Institutes of Health grant DK46269.

Article, publication date, and citation information can be found at http://molpharm.aspetjournals.org.

doi:10.1124/mol.107.035352.

ABBREVIATIONS: ACA, N-(p-amylcinnamoyl) anthranilic acid; AACOCF₃, arachidonyl trifluoromethyl ketone; BPB, p-bromophenacyl bromide; CUBS cell line, human embryonic retinal pigment epithelium cells stably transfected with hNaDC1; Fmoc-anthranilic acid, N-(9-fluorenylmethoxycarbonyl)-anthranilic acid; HRPE, embryonic human retinal pigment epithelium; NaDC1, Na⁺/dicarboxylate cotransporter 1; ONO-RS-082, 2-(p-amylcinnamoyl) amino-4-chloro benzoic acid; PLA₂, phospholipase A₂; rb, rabbit; Tranilast, N-(3', 4'-dimethoxycinnamoyl) anthranilic acid; Sulfo-NHS-LC-Biotin, sulfosuccinimidyl-6-(biotinamido) hexanoate.

Address correspondence to: Dr. Ana M. Pajor, Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555-0645. E-mail: ampajor{at}utmb.edu

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