Methods for transporting vitamin C transporter and related methods

Abstract

The invention provides methods for regulating the transport of vitamin C across membranes.

Description

BACKGROUND OF THE INVENTION

[0002] 1. Field of the Invention

[0003] The present invention relates to transcellular transport or cellular uptake of vitamin C (L-ascorbate), and in particular to compositions encoding transport proteins for vitamin C and methods for its preparation and use.

[0004] 2. Background Information

[0005] Vitamin C is an essential multi-functional micronutrient required in its reduced form (L-ascorbic acid) for many enzymatic reactions and as a scavenger of free radicals generated from numerous physiological and pathological processes. It has been known for more than 70 years that vitamin C is essential to the human body, and the disease scurvy, caused by an extreme deficiency of vitamin C, has been known for hundreds of years. But surprisingly, little has heretofore been discovered about how the body actually absorbs vitamin C, and how the vitamin is distributed to the many organs at appropriate concentrations to ensure crucial enzymatic reactions (e.g., collagen synthesis) and to protect tissues and organs from oxidative damage.

[0006] Several facilitative hexose transporters (of the GLUT family) are known to transport dehydroascorbic acid (but not L-ascorbic acid) in vitro. Although the oxidized form of the vitamin has the same oral bioactivity as L-ascorbic acid, the GLUT-type transporters are unlikely to account for significant absorption of the vitamin as long as glucose is present in the lumen. Whereas several human cell types have been shown to possess high capacity dehydroascorbic acid transport activity in vitro, these systems may have only limited physiological significance because vitamin C is present in human plasma essentially only in its reduced form, so the GLUT systems would not be expected to participate in the cellular uptake of the vitamin. The exception is in the “recycling” of the oxidized vitamin, e.g., in activated neutrophils or erythrocytes, under conditions in which the extracellular dehydroascorbic acid concentration may be locally high.

[0007] There are numerous suggestions in the literature regarding the involvement of vitamin C in a variety of human diseases. Studies indicate that vitamin C levels are reduced in the elderly, smokers, and cancer patients, and that defective serum antioxidant status contributes to the increased oxidative stress associated with many diseases. For example, oxidative stress in the central nervous system (CNS) may cause oxidation of lipoprotein, which can itself initiate the neuronal cell death leading to the manifestation of neurodegenerative diseases. Epidemiological research suggests that dietary vitamin C supplementation is effective in the prevention of various types of cancer, including bladder, breast, cervical, colorectal, esophageal, lung, pancreatic, prostate, salivary gland, stomach, leukemia, and non-Hodgkin's lymphoma. Vitamin C may also play a protective role in atherogenesis, since epidemiological studies indicate that plasma ascorbic acid levels are inversely related to mortality due to coronary heart disease.

DESCRIPTION OF THE INVENTION

[0008] Brief Summary of the Invention

[0009] One aspect of the invention comprises, as a composition of matter, a non-naturally occurring vitamin C-transporter protein. The transporter protein is found to exist in two forms, referred to herein as SVCT1 and SVCT2. Localization studies demonstrate that SVCT1 is largely confined to bulk-transporting epithelia such as intestine and kidney, where it serves whole-body homeostasis. SVCT2 appears to account for the widespread tissue-specific uptake of vitamin C, and is found in neural, endocrine, exocrine and endothelial tissues as well as in osteoblasts. In the eye, SVCT2 likely transports vitamin C into the aqueous humor, the cornea and the lens (where the vitamin is required at high concentration for protection against UV radiation and oxidative stress). On the other hand, excessive vitamin C accumulation may promote the growth of astrocytic brain tumors (gliomas).

[0010] The cloning of these transporters facilitates understanding of how they function to regulate an appropriate supply of the vitamin in various tissues and the role they play in protection against oxidative stress. This advance also facilitates identification of therapeutic opportunities involving vitamin C (e.g., for protection against viral infections (such as the common cold), cataract, and certain types of cancer and leukemias).

[0011] Preferably, the transporter is a polypeptide encoded by a nucleic acid sequence within SEQ ID NO: 1, 3, 5, or 6. In this context, the term “encoded” refers to an amino-acid sequence whose order is derived from the sequence of the nucleic acid or its complement. The nucleic acid sequences represented by SEQ ID NOS:1 and 2 are derived from human sources. The nucleic acid sequences represented by SEQ ID NOS: 5 and 6 are derived from rat.

[0012] Accordingly, one embodiment of this aspect of the invention is directed toward an isolated transporter having an amino-acid sequence substantially corresponding at least to the conserved regions of SEQ ID NO: 3, 4, 7 or 8. The term “substantially,” in this context, refers to a polypeptide that may comprise substitutions and modifications that do not alter the physiological activity of the protein to transport calcium across cellular membranes. The polypeptide represented by SEQ ID NO: 2 is derived from human sources. The peptide represented by SEQ ID NO: 4 is derived from rat. The protein does not retain functionality as a free species. Thus, by “isolated” is meant integral with a cellular membrane or other lipid bilayer, or stabilized by an appropriate detergent (e.g., TRITON X-100, a surfactant available from Rohm & Haas, Philadelphia, Pa.).

[0013] In a second aspect, the invention pertains to a non-naturally occurring nucleic acid sequence encoding a vitamin C-transporter protein. One embodiment of this aspect of the invention is directed toward a transporter having a nucleotide sequence substantially corresponding at least to the conserved regions of SEQ ID NO: 1, 2, 5, or 6. The term “substantially,” in this context, refers to a nucleic acid that may comprise substitutions and modifications that do not alter encoding of the amino-acid sequence, or which encodes a polypeptide having the same physiological activity in transporting vitamin C across cellular membranes. The term “corresponding” means homologous or complementary to a particular nucleic-acid sequence.

[0014] A third aspect of the invention comprises methods of using a membrane protein that functions to transport vitamin C across cellular membranes. One aspect of this embodiment of the invention comprises methods associated with a non-naturally occurring vitamin C-transporter protein. Once again, the transporter is preferably a polypeptide encoded by a nucleic acid sequence within SEQ ID NO: 1, 2, 5, or 6. Another aspect of this embodiment is directed toward uses of a transporter having an amino-acid sequence substantially corresponding at least to the conserved regions of SEQ ID NO: 3, 4, 7, or 8.

[0015] A fourth aspect of the present invention comprises a method of transporting vitamin C across a cellular membrane having a sodium-coupled protein transporter in accordance herewith. Vitamin C (as L-ascorbate or L-ascorbic acid) is applied to the cellular membrane under conditions that facilitate its transmembrane penetration (cellular uptake) via the transporter.

[0016] In a fifth aspect, the invention comprises a method of identifying chemicals capable of interacting with the transporter, whether the protein is integral with a cellular membrane or other lipid bilayer, or stabilized by an appropriate detergent. Such chemicals may include antibodies or other targeting molecules that bind to the protein for purposes of identification, or which affect (e.g., by modulation or inhibition) the transport properties of the protein; products of combinatorial chemistry libraries; and transportable species other than vitamin C.

[0017] In a sixth aspect, the invention comprises a method of blocking or inhibiting or activating the uptake of vitamin C by cells having a transporter protein in accordance herewith. In one embodiment, the method comprises the steps of causing an antibody or other targeting molecule to bind to the protein in a manner that inhibits or activates vitamin C transport. In another embodiment, a nucleic acid complementary to at least a portion of the nucleic acid encoding the transporter protein is introduced into the cells. The complementary nucleic acid blocks or activates functional expression of the vitamin C transporter protein. In still another embodiment, an inhibitor such as phloretin is applied to the transporter.

[0018] In a seventh aspect, a drug is linked to a transported species in a cleavable manner. This facilitates oral administration of the drug, which is absorbed, with the transported species, into intestinal enterocytes. The drug is then cleaved from the transported species either within the cell or through hepatic metabolism (following its exit into the bloodstream). SVCT1 and SVCT2 are each saturable, exhibiting high apparent affinity for L-ascorbic acid (K0.5=50-100 μM), and Na+-dependent. A coupling stoichiometry of 2 Na+:1 L-ascorbic acid for SVCT1 may be inferred based upon the following experimental observations: SVCT1-mediated L-ascorbic acid transport is both Na+-dependent and electrogenic, generating inward currents (i.e., net inward positive-charge movements), despite transport of L-ascorbic acid in its deprotonated (1−) form (given the effective pH range of the transporter). This stoichiometry is further supported by the observation that two Na+ ions are required to activate the transporter (from the Hill coefficient, based on voltage-clamp experiments).

[0019] SVCT1 is stereospecific and intensely favors L-ascorbic acid over D-isoascorbic acid, dehydroascorbic acid, L-ascorbic acid-2-phosphate and L-ascorbic acid-6-palmitate. SVCT1 transport activity is sensitive to changes in extracellular pH (optimum pH ≈7.5), which may affect the binding affinity for L-ascorbic acid.

[0020] Human and rat SVCT1 and SVCT2 were found to be discretely distributed. SVCT1 had a limited distribution, mainly confined to the bulk transporting epithelia such as kidney and small intestine, but was also present in a few endocrine tissues, including a 9-kb transcript in human thymus. SVCT2 displayed a much broader distribution in brain, retina and spleen, and in several endocrine and neuroendocrine tissues. The possibility that SVCT1 and SVCT2 are localized to different cell types or to different membranes (apical or basolateral) within polarized epithelial cells has not been established. Alternatively, the fact that these two transporters share very similar functional characteristics yet remain discretely distributed may suggest that they are differentially regulated.

BRIEF DESCRIPTION OF THE DRAWINGS

[0021] The foregoing discussion will be understood more readily from the following detailed description of the invention, when taken in conjunction with the accompanying drawings, in which:

[0022] FIG. 1 illustrates the aligned amino acid sequences of human SVCT1 (SEQ ID NO: 3), rat SVCT1 (SEQ ID NO: 7), mouse SVCT1 (SEQ ID NO: 9), human SVCT2 (SEQ ID NO: 4), rat SVCT2 (SEQ ID NO: 8), and pig SVCT2 (SEQ ID NO: 10), with conserved residues shaded and the twelve putative transmembrane domains underlined and numbered;

[0023] FIG. 2 is a Kyte-Doolittle hydrophobicity plot of rat SVCT1 and SVCT2, generated using a 21-amino-acid window;

[0024] FIG. 3 is a membrane-topology model of rat and human SVCT1 based on hydropathy profiles;

[0025] FIG. 4A depicts typical current recordings from a voltage-clamped (1-50 mV) control oocyte or oocytes expressing rat SVCT1 and SVCT2, all from a single batch of oocytes (the approximate baseline current in standard Na+ medium at pH 7.5 is indicated by dashed lines);

[0026] FIG. 4B depicts the current/voltage (I/V) relationship for rat SVCT1 at 500 μM (saturating) L-ascorbic acid (at 100 mM Na+);

[0027] FIG. 4C illustrates L-ascorbic acid saturation kinetics for rat SVCT1 at 100 mM Na+ and at −50 mV;

[0028] FIG. 4D illustrates Na+ saturation kinetics of the currents evoked by 2001M L-ascorbic acid for rat SVCT1 at −50 mV;

[0029] FIG. 4E depicts the effect of Na+ on the I/V relationship for rat SVCT1 (at 200 μM L-ascorbic acid);

[0030] FIG. 4F demonstrates the substrate selectivity of rat SVCT1;

[0031] FIG. 4G shows a comparison of currents due to Na+ leak (uniport) and Na+/L-ascorbic acid co-transport;

[0032] FIG. 4H illustrates phloretin (Pt) inhibition of the L-ascorbic acid-evoked current in rat SVCT1;

[0033] FIG. 4I illustrates a Dixon analysis of phloretin inhibition;

[0034] FIG. 4J shows the pH dependence of L-ascorbic acid-evoked currents in rat SVCT1;

[0035] FIG. 5 is an ideogram of human chromosome 5 showing the location of the gene encoding SVCT1;

[0036] FIG. 6 illustrates the genomic localization of the SLC23A2 and MATRIN3 genes;

[0037] FIG. 7 graphically illustrates the transport characteristics of SVCT1 expressed in oocytes based on [14C]ascorbate isotope flux studies;

[0038] FIG. 8A graphically illustrates the results of voltage-clamp experiments to determine transport properties, and shows typical current recordings from (1) a control oocyte and (2) an oocyte expressing human SVCT1 from the same batch;

[0039] FIG. 8B shows the pH dependence of L-ascorbic acid-evoked currents in human SVCT1;

[0040] FIG. 9 demonstrates the substrate selectivity of human SVCT1; and

[0041] FIG. 10 graphically illustrates L-ascorbic acid transport activity associated with human SVCT2 based on isotope flux studies.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0042] 1. SVCT1, SVCT2 and Their Nucleic Acids

[0043] With reference to SEQ ID NO: 1, a human-derived cDNA having a nucleotide sequence encoding SVCT1, a vitamin C-transport protein, contains 2306 nucleotides; an open reading frame of 1797 base pairs (bp) (i.e., nucleotides 48-1844) encodes the SVCT1 protein comprised of 598 amino acids, which is set forth as SEQ ID NO: 3. With reference to SEQ ID NO: 2, a human-derived cDNA having a nucleotide sequence encoding a SVCT2, a vitamin C-transport protein, contains 2010 nucleotides; an open reading frame of 1950 bp encodes a protein having 650 amino acids, which is set forth as SEQ ID NO: 4.

[0044] SEQ ID NOS: 5 and 6 are rat-derived cDNA having nucleotide sequences encoding SVCT1 and SVCT2, respectively. Rat SVCT1 contains 2472 nucleotides, and an open reading frame of 1812 bp encodes the rat SVCT1 protein comprised of 604 amino acids, which is set forth as SEQ ID NO: 7. Rat SVCT2 contains 4001 nucleotides, and an open reading frame of 1776 bp encodes the rat SVCT1 protein comprised of 592 amino acids, which is set forth as SEQ ID NO: 8. Rat SVCT2 has 65% amino-acid identity to SVCT1. As illustrated in FIG. 1, the amino-acid sequences for each isoform (SVCT1 or SVCT2) showed over 90% identity across different species (human, rat, mouse, pig) and ≈65% identity between the SVCT1 and SVCT2 isoforms from different species. HSVCT 1 comprises 598 amino acid residues and is almost identical to a sequences designated YSPL3. SVCT1 and SVCT2 also show 34% sequence identity to the mouse yolk-sac permease-like (mYSPL1) protein of unknown function and 20-30% identity to putative nucleobase transporters in bacteria, yeast, and plants.

[0045] Both human and rat SVCT1 and SVCT2 proteins have similar hydropathy profiles, all predicting 12 putative membrane-spanning domains as shown and numbered in FIG. 2. The SVCT1 sequence comprises consensus sites for protein kinases A and C, and N-linked glycosylation. Comparison of the translation products in the presence or absence of microsomes revealed a 15-kilodalton gel shift, suggesting that at least two of the consensus sites in SVCT1 are glycosylated in vivo.

[0046] 2. Isolation and Analysis of SVCT1 and SVCT2

[0047] To clone the genes encoding SVCT1 and SVCT2, an expression cloning strategy using Xenopus laevis oocytes as the expression system was employed. It is noted, however, that expression cloning can also be achieved using other mammalian cells, yeast cells, bacterial cells, insect cells, plant cells, or brush border membrane vesicles.

[0048] Rat SVCT1 and SVCT2 clones were obtained by isolating SVCT1 cDNA from rat kidney by expression cloning as described in Hediger et al., Methods Enzymol. 296:17-52 (1998). The SVCT2 cDNA was subsequently isolated by PCR-based homology screening of a rat brain cDNA library. A 2.5-kb rabbit cDNA with 96% identity to residues 96-505 of the rat SVCT2 was obtained by RT-PCR. Radiotracer and voltage-clamp experiments were performed (at 22° C.) in Xenopus oocytes two to seven days after injection with ˜25 ng of SVCT1 or SVCT2 cRNA synthesized in vitro. Radiotracer uptake was determined by incubating 6-10 oocytes for 30 or 60 min in standard 100 mM Na+ or Na+-free media with 10-600 μM L-[14C]ascorbic acid.

[0049] The experimental procedures employed, and the results obtained, were as follows.

[0050] 2.1 Rat SVCT1 and SVCT2

[0051] Cloning of SVCT cDNAs—SVCT1 cDNA was isolated from rat kidney by expression cloning with heterologous expression in Xenopus oocytes. Briefly, poly(A)+ RNA was extracted from kidney cortex of normal male Sprague-Dawley rats. This poly(A)+ RNA induced a 30-fold increase in Na+-dependent L-[14C]ascorbic acid uptake activity in oocytes compared with control (water-injected) oocytes. Poly(A)+ RNA was size-fractionated using preparative gel electrophoresis, and a positive poly(A)+ RNA fraction inducing maximal L-[14C]ascorbic acid uptake activity (1.5-fold enrichment over non-fractionated poly(A)+ RNA) was used to construct a directional cDNA library with the SuperScriptII cDNA synthesis system (supplied by GibcoBRL). cDNA pools (of ≈2.5×104 clones each) were screened. A positive pool that increased transport activity to a degree similar to kidney cortex poly(A)+ RNA was sequentially subdivided and analyzed until a single clone (SVCT1) was identified.

[0052] SVCT2 cDNA was isolated by PCR-based homology screening of a rat brain cDNA library. First-strand cDNA was prepared by reverse transcription from rat brain poly(A)+ RNA. Sense and antisense degenerate oligonucleotide primers were designed based upon the SVCT1 cDNA sequence (sense, ATH GAR TCN ATH GGN GAY TA (SEQ ID NO: 11), coding for amino acid residues 339-346 of SVCT1, and antisense, CC RM RAA DAT NGA RAA NCC (SEQ ID NO: 12), residues 468-475) and used for PCR amplification of the brain cDNA. PCR products of the expected size (≈400 bp) were subcloned into the pCRII vector (Invitrogen) and sequenced. A single clone with 80% identity to SVCT1 was labelled using [32P]-dCTP and used to screen a rat brain cDNA library constructed in the λgt10 vector. The library (≈4×105 clones) was screened under high-stringency conditions by washing with 0.1×SSC and 0.1% SDS at 65° C. for 1 h. A positive clone of a 6.5 kb cDNA was isolated and subcloned into pBluescript SK(−). The cDNA sequence was determined on both strands and analyzed using Genetics Computer Group tools. To improve expression in oocytes, an EcoRI site was introduced to the 5′-untranslated region (nucleotide 198) using PCR. Two 6.5-kb SVCT2 cDNA fragments obtained by EcoRI-EcoRI (1.5 kb) and EcoRI-SphI (0.5 kb) digestions, were ligated and subcloned into a blunt-ended dephosphorylated NotI site in the vector pTLN2.

[0053] A rabbit cDNA (rbSVCT2) of 1.2-kb in length and with 96% identity to residues 96 to 505 of the rat SVCT2 was obtained by reverse transcription-PCR from rabbit brain mRNA using a set of rat SVCT2 oligonucleotide primers (sense, nucleotides 660-682; antisense, nucleotides 1870-1892). Sequence alignments were performed using the PILEUP program from Genetics Computer Group (Madison, Wis.).

[0054] Functional characterization of SVCT1 and SVCT2 in Xenopus oocytes—Oocytes were isolated from Xenopus laevis (under 2-aminoethylbenzoate anaesthesia), treated with collagenase A and stored at 18° C. in modified Barths' medium. Oocytes were injected with 25 ng of SVCT1 or SVCT2 cRNA synthesized in vitro, or water only (control), and incubated 2-7 days before radiotracer or voltage-clamp experiments were performed. Standard Na+ uptake medium comprised 100 mM NaCl, 2 mM KCl, 1 mM CaCl2, 1 mM MgCl2, 10 mM HEPES (pH 7.5 with Tris base). For Na+-free or low-Na+ media, NaCl was replaced by equimolar choline chloride; likewise, Cl− was replaced by gluconate for Cl−-free medium. For pH-sensitivity experiments, Na+ media were buffered at pH 5.5-8.0 using 0-5 mM MES, 0-5 mM HEPES and 0-5 mM Tris base. L-Ascorbic acid-containing solutions were freshly-prepared (without dithiothreitol) and used immediately.

[0055] Radiotracer uptake was determined by incubating 6-10 oocytes for 30 or 60 min in standard Na+ or Na+-free media (at 22° C.) with 10-600 μM L-[1-14C]ascorbic acid (final specific activity 0.3 GBq/mmol). Oocytes were solubilized with 10% SDS and [14C]-content was measured by liquid scintillation counting. A two-microelectrode voltage-clamp was used to measure currents in control oocytes and oocytes injected with rat SVCT1 or rat SVCT2 cRNA. Microelectrodes (resistance 0.5-5 MQ) were filled with 3 M KCl. Oocytes were superfused at 22° C. in standard Na+ medium and clamped at a holding potential (Vh) of −50 mV. For continuous current monitoring at Vh=−50 mV, the current was low-pass filtered at 20 Hz (sampling at 1 Hz). Additionally, step-changes in membrane potential (Vm) were applied (from +50 mV to −150 mV in 20-mV increments), each for a duration of 100 ms, before and after the addition of substrate; current was low-pass filtered at 500 Hz and digitized at 5 kHz. Test solutions were always washed out with substrate-free medium (100 mM choline chloride) at pH 7.5 for several minutes. Steady-state data (obtained by averaging the points over the final 16.7 ms at each Vm step when step-changes were applied) were fitted to equation (1) below, for which/is the evoked current (i.e., the difference in steady-state current measured in the presence and absence of substrate), Imax the derived current maximum, S the concentration of substrate S (Na+ or L-ascorbic acid), 1$K_{0.5}^S$

[0056] the substrate concentration at which current was half-maximal, and nH the Hill coefficient for S. (For radiotracer experiments, I was replaced with velocity V and Imax replaced with the derived maximal velocity, Vmax.) 2$\begin{array}{cc}I=\frac{I_{\max }·S^{n_H}}{{\left(K_{0.5}^S\right)}^{n_H}+S^{n_H}}& \left(1\right)\end{array}$

[0057] Observed data indicate that SVCT1 and SVCT2 each mediate saturable, Na+-dependent L-ascorbic acid transport in an electrogenic manner. L-[14C]Ascorbic acid uptake (in 100 mM NaCl) followed Michaelis-Menten-type saturation kinetics with high apparent affinity for L-ascorbic acid. Uptakes were not affected by replacement of chloride with gluconate, indicating that neither isoform was Cl−-dependent.

[0058] In the presence of Na+, L-ascorbic acid evoked reversible inward currents of up to −100 nA in oocytes expressing SVCT1 and up to −10 nA in oocytes expressing SVCT2 (FIG. 4A). Evoked currents in control oocytes were −1 nA±0.5 nA (s.d.) at 500 μM L-ascorbic acid. Transporter-associated currents were investigated in detail for SVCT1 and, where possible, our findings were supported by data from radiotracer experiments for SVCT1 and SVCT2. In oocytes expressing SVCT1, the L-ascorbic acid-evoked currents (at saturating L-ascorbic acid) showed a curvilinear dependence on membrane potential (Vm) (FIG. 4B), saturating with hyperpolarization (−70 mV). The current/voltage relationship was roughly linear between −50 mV and +30 mV (tending toward a zero current asymptote at positive Vm) with no reversal of the currents observed up to +50 mV. At −50 mV, 3$K_{0.5}^{\mathrm{Asc}}$

[0059] (L-ascorbic acid concentration at which currents were half-maximal) was 30 μM (FIG. 4C) with nH 1. The Hill coefficient (nH) for Na+ was ≈2 (FIG. 4D). 4$K_{0.5}^{\mathrm{Na}}$

[0060] (at 200 μM L-ascorbic acid) was 40 mM at −50 mV; 5$K_{0.5}^{\mathrm{Na}}$

[0061] was not significantly different at hyperpolarized Vm, but rose at depolarized Vm. These data suggested that two Na+ bind to SVCT1 and that binding is voltage-sensitive. SVCT1-mediated L-ascorbic acid transport is driven by the electrochemical gradient for Na+ since, at any given Vm, the current evoked by 200 μL-ascorbic acid was greatest at higher Na+ concentrations (FIG. 4E). The evoked currents obtained at 100 mM Na+ saturated at less negative Vm, and with a larger maximal current than those obtained at 50 and 20 mM Na+. Following step-changes in voltage, SVCT1 exhibited presteady-state currents (decaying with time constants 10-40 ms). These presteady-state currents were sensitive to changes in extracellular Na+ concentration and (in analogy to other ion-coupled transporters) are due in part to binding/dissociation of the driving ion (in this case Na+) to the transporter. Switching from 0 to 100 mM Na+ in the absence of L-ascorbic acid resulted in a small inward current in control oocytes (FIGS. 4A, 4G) but a much larger current in oocytes expressing either SVCT1 or SVCT2. Addition of L-ascorbic acid in the presence of Na+ evoked still larger inward currents. These observations suggested that SVCT1 and SVCT2 can additionally exhibit a Na+ leak (uniport) current (similar to the leak pathways in other ion-coupled transporters) that is as much as half the magnitude of the current associated with Na+/L-ascorbic acid cotransport (FIG. 4G).

[0062] As shown in FIG. 4F, SVCT1 was highly selective for L-ascorbic acid, which evoked much larger currents than did D-isoascorbic acid (30% that for L-ascorbic acid) or dehydroascorbic acid (≈5%). (Dehydroascorbic acid failed to evoke a current in control oocytes.) D-Glucose, uracil, and intermediates of vitamin C metabolism (such as L-gulono-γ-lactone) were excluded. Several test compounds, including aspirin (acetylsalicylic acid), xanthine, sulfinpyrazone and phlorizin, each evoked tiny outward currents in oocytes expressing SVCT1 and resulted in modest inhibition of the SVCT1- or SVCT2-mediated L-[14C]ascorbic acid uptake—i.e., they exhibited characteristics of weak blockers. Phloretin evoked a sizable outward current in oocytes expressing SVCT1 (FIG. 3F). This effect is probably attributable to phloretin blocking the Na+ leak current. In addition, phloretin blocked the inward current evoked by L-ascorbic acid (FIG. 4H) and inhibited L-[14C]ascorbic acid uptake by SVCT1 or SVCT2. Dixon analysis of L-[14C]ascorbic acid uptake for SVCT1 (FIG. 41) revealed that phloretin was a non-competitive inhibitor with Ki≈65 μM. Meanwhile, phloretin inhibited the Na+ leak current with apparent Ki≈100 μM. The similarity of these values for the effects of phloretin on both the cotransport and uniport modes of the transport cycle suggests that phloretin interacts with SVCT1 at a single locus on the protein. The evoked currents in SVCT1 were sensitive to changes in extracellular pH (FIG. 4J). Those at pH 5.5 were 50% smaller than those at pH 7.5 but were partially restored by the addition of excess L-ascorbic acid (5 mM). A similar pattern of pH-sensitivity was observed for SVCT2 in radiotracer experiments. This pH-sensitivity is probably a result of reduced binding affinities for L-ascorbic acid rather than less available L-ascorbic acid in the deprotonated (1−) form, since >95% is in the deprotonated form at pH 5.5 (pka1=4.2). Although the small currents obtained for SVCT2 hampered its characterization, radiotracer experiments did not reveal any functional differences between the SVCT isoforms. The activities described for SVCT1 and SVCT2 expressed in oocytes were consistent with those described for several mammalian tissues (in vesicles, isolated tissues or cultured cell lines) with regard to the following characteristics: (i) high apparent affinity for L-ascorbic acid (K0.5Asc of 10-100 μM); (ii) a preference for L-ascorbic acid>D-isoascorbic acid>dehydroascorbic acid; and (iii) Na+ dependence.

[0063] Northern-blot analysis—Total RNA was isolated from rat tissues and cell culture of murine MC3T3-E1 osteoblasts followed by oligo(dT) selection. Poly(A)+ RNA (3 μg/well) was separated on a formaldehyde-agarose (7%/1%) gel and blotted onto a nitrocellulose filter. A 0.35-kb BglII digestion product from SVCT1 cDNA (nucleotides 425-773) and a 3.1-kb HindIII digestion product of SVCT2 cDNA (nucleotides 1-3101) were labelled with [32P]-dCTP. The filters were hybridized at 42° C. in 50% formamide, and washed in 5×SSC/0.1% SDS at 50° C. for 2×30 min, then in 0.1×SSC/0.1% SDS at 65° C. for 3×20 min.

[0064] Striking differences between SVCT1 and SVCT2 in terms of tissue distribution in rat were found. Northern-blot analysis using a probe for SVCT1 revealed intense bands at ≈2.5 kb and ≈4.0 kb in rat kidney, intestine, and liver, whereas probing for SVCT2 RNA resulted in a weaker signal at ≈6.5 kb for those tissues. Using in situ hybridization of rat tissues, SVCT1 was localized to the straight segment (S3) of the proximal tubule in the kidney, consistent with studies of rat kidney L-ascorbic acid transport in vitro. In the small intestine, SVCT1 and SVCT2 mRNAs were present in enterocytes. In liver, SVCT1 but not SVCT2 was detected in hepatocytes. Both isoforms were detected in epithelial cells of the bronchiole and epididymis.

[0065] SVCT2 was abundantly expressed in an array of neural, neuroendocrine, exocrine and endothelial tissues as well as in osteoblasts. In Northern-blot analysis of rat tissue, a strong SVCT2 signal was obtained for brain at ≈6.5 kb. The mRNA was localized to neurons throughout the CNS. The distribution closely matched the sites of rapid neuronal accumulation observed in mouse brain following intravenous L-[14C]ascorbic acid injection and is consistent with the view that neurons take up L-ascorbic acid (released by astroglia). SVCT2 was also detected in the meninges and choroid plexus, suggesting that SVCT2 may facilitate entry of L-ascorbic acid into the cerebrospinal fluid compartments. In the retina, SVCT2 labelling was observed exclusively in the inner nuclear layer (the site of bipolar, amacrine, and horizontal cell bodies).

[0066] L -Ascorbic acid is believed to be crucial in protecting components of the eye (e.g., the lens and cornea) from radiation-induced damage. Since the levels of L-ascorbic acid in the aqueous humor (anterior chamber) in diurnal mammals can be around 20-fold greater than in nocturnal mammals, investigations were undertaken to determine whether the distribution of SVCT isoforms in the eye differed between the rat (nocturnal) and the rabbit (diurnal-nocturnal). In the rat, neither SVCT1 nor SVCT2 was detected in the ciliary body (which secretes aqueous humor) or iris. However, in the albino rabbit, SVCT2 was abundantly expressed in the pigmented epithelium of the ciliary body, and moderately expressed in the deeper layers of the corneal epithelium. This SVCT2 distribution was consistent with the known sites of L-ascorbic acid concentration in the rabbit eye, and the characteristics of SVCT2 reflected those of a Na+-dependent, L-ascorbic acid transport activity expressed in bovine pigmented ciliary epithelial cells. In the rat, SVCT1 and SVCT2 were each detected in exocrine cells of the lacrimal gland; there, the supply of L-ascorbic acid to the tear fluid may provide sufficient anti-oxidant protection in nocturnal species.

[0067] SVCT2 was expressed in several components of the endocrine system, including the anterior pituitary, in which L-ascorbic acid is important in α-amidation of peptide hormones. Labelling was also observed in the intermediate lobe but not in the posterior lobe. SVCT2 was abundantly expressed throughout the pancreas and in adrenal cortex. In the adrenal gland, L-ascorbic acid is critical for the copper-associated dopamine-β-hydroxylase involved in noradrenalin synthesis. SVCT2 was detected in gastric glands, extending from the base to the isthmus. Autoradiographic studies in mouse demonstrated rapid accumulation of L-ascorbic acid into the gastric mucosa following intravenous injection. Taken together these observations implicate SVCT2 in the basolateral uptake of L-ascorbic acid, for secretion by the gastric gland, aiding dietary iron absorption. An intense SVCT2-related signal was obtained in Northern-blot analysis of poly(A)+ RNA from the murine osteoblast MC3T3-E1 cell line. SVCT2-mediated L-ascorbic acid transport into osteoblasts may account for the adequate supply of the vitamin to maintain Fe2+ required by hydroxylases involved in collagen synthesis. Among immune system organs, SVCT2 was detected by Northern-blot in the spleen and thymus. In testis, SVCT2 was expressed in interstitial cells and spermatocytes.

[0068] In situ hybridization-Digoxigenin-labelled antisense and sense run-off transcripts were synthesized using the Genius Kit (supplied by Boehringer-Mannheim). Rat SVCT1 cRNA probes were transcribed from a PCR fragment that contained about 1.2 kb of SCVT1 cDNA (nucleotides 161-1411) flanked by promoter sites for SP6 and T7 polymerase. Rat SVCT2 cRNA probes were transcribed from a plasmid vector pBluescript SK(B) which contained 3.1 kb of the SVCT2 sequence (nucleotide 1 to 3101). Transcripts were alkali-hydrolyzed to an average length of 200-400 nucleotides. In situ hybridization was performed on 10-μm cryosections of fresh-frozen tissue. Sections were immersed in slide mailers in hybridization solution of composition 50% formamide, 5×SSC, 2% blocking reagent, 0.02% SDS and 0.1% N-laurylsarcosine, and hybridized at 70° C. for 16 h with probe concentrations of ≈200 ng/ml. Sections were then washed 3 times in 2×SSC and for 2×30 min in 0.2×SSC at 70° C. The hybridized labelled probes were visualized using anti-digoxigenin Fab fragments and BCIP/NBT substrate. Sections were developed in substrate solution for 16 h, rinsed in 100 mM Tris, 100 mM NaCl, 1 mM EDTA (pH 9.5), and coverslipped. For in situ hybridization of rbSVCT2 in rabbit, sense and antisense rbSVCT2 cRNA probes were prepared by RT-PCR based on the same oligonucleotide sequence from rat SVCT2 additionally flanked by the SP6 and T7 RNA polymerase promoter sequences. In situ hybridization was performed on 10-μm cryosections from the eye of a New Zealand albino rabbit (as described above for rat).

[0069] Hybrid depletion-Antisense oligonucleotides were generated against nucleotides 18-42 of rat SVCT1, and against nucleotides 383-405 of rat SVCT2. These were annealed (at 0.25 μg/μl, in 50 mM NaCl at 42° C.) for 15 min with 0.5 μg/μl poly(A)+ RNA isolated from rat kidney cortex, small intestine or adrenal glands. Samples were then cooled on ice and injected into oocytes (≈25 ng/oocyte), before performing radiotracer assays as described above. The efficacy of the annealing process, and the suitability of the antisense oligonucleotides, was established using SVCT1 or SVCT2 cRNA. It was found that annealing with the appropriate antisense oligonucleotide abolished L-ascorbic acid transport activity, with no appreciable cross-inhibition between SVCT isoforms.

[0070] L -[14C]Ascorbic acid uptake was 3-fold higher in oocytes injected with intestinal RNA than in control oocytes. The induced activity was Na+-dependent (not shown) and abolished by hybridization with antisense oligonucleotide against SVCT1, suggesting that SVCT1 is the predominant L-ascorbic acid transport system in the small intestine. Similar results were obtained for kidney, and data for adrenal gland suggested that expression of SVCT2 and SVCT1 can together account for the increased uptake in RNA-injected oocytes. Therefore SVCT1 and SVCT2 appear to be the predominant L-ascorbic acid transport systems (at least for 6$K_{0.5}^{\mathrm{Asc}}$

[0071] of similar order) in the tissues tested.

[0072] 2.2. Human SVCT1 and SVCT2

[0073] Molecular cloning of human SVCT1 cDNA—RNA was isolated from human kidney by guanidinium isothiocyanate/CsCl centrifugation followed by poly(A)+ selection using oligo(dT)-cellulose columns. A λgt10 cDNA library was constructed from the human kidney poly(A)+ RNA using the SuperScript II cDNA synthesis kit (from Life Technologies). cDNA was synthesized using an oligo(dT) primer and ligated to EcoRI-NotI adaptors. cDNA fragments of 2-4 kilobases (kb) in length were isolated and ligated to EcoRI-cleaved λgt10 DNA. After packaging using the Gigapack II Gold cloning kit (from Stratagene), phage (4H 105 pfu) was plated and transferred to replicate filters. A human EST clone (accession number M811090) homologous with rat SVCT1 (AF080452) was labeled with [32P]-dCTP. The filters were then hybridized with the EST probe overnight at 42° C. in buffer containing 50% formamide, 5×SSC, 50 mM sodium phosphate (buffered to pH 6.8), 2× Denhardt's solution, and 100 mg/ml denatured salmon sperm DNA. The filters were washed under high stringency conditions (0.1×SSC and 0.1% SDS at 65° C. for 1 h). Positive clones were isolated and subcloned into pBluescript SK(−) vector. cDNA fragments were sequenced and analyzed using GCG tools (from Genetics Computer Group) to identify human clones related to SVCT1 previously cloned from rat and rabbit as described above.

[0074] Construction of the human SVCT2 cDNA—Oligonucleotide primers (5′ ATG ATG GGT ATT GGT MG AAT ACC 3′ (SEQ ID NO: 13) and 5′ AGC MG GAA CTA CAG ATA CAT GCC 3′ (SEQ ID NO: 14)) based on the YSPL2 sequence (listed in GenBank as human SVCT2, and with accession number AF058319) and a similar sequence (D87075) were used for RT-PCR amplification, using the Advantage cDNA PCR kit (from Clontech) and human kidney total RNA, to generate the human SVCT2 cDNA (2010 bp), the identity of which was confirmed by partial sequencing (≈500 bp) from the 5′ end.

[0075] Functional characterization in Xenopus oocytes—SVCT1 and SVCT2 cDNAs were subcloned into the pTLN2 vector (to improve functional expression in oocytes) and used for cRNA synthesis in vitro using the MEGAscript kit and T7 RNA polymerase (from Ambion). Oocytes were isolated from Xenopus laevis, treated with collagenase A and maintained at 18° C. in modified Barths' medium. Oocytes were injected with 15 ng SVCT1 or SVCT2 cRNA or water only. The radiotracer uptake and voltage-clamp experiments described below were conducted 2-5 days post-injection in standard medium of composition 100 mM NaCl, 2 mM KCl, 1 mM CaCl2, 1 mM MgCl2, and 10 mM HEPES (buffered to pH 7.5 with Tris base). For low-Na+ or Na+-free media, NaCl was replaced with choline chloride. For pH-dependence experiments, Na+ media were buffered to between pH 5.5 and pH 8.0 using 0-5 mM MES, 0-5 mM HEPES and 0-5 mM Tris base. L-Ascorbic acid-containing solutions were always freshly prepared and used immediately. Radiotracer uptake was determined by incubating 8-12 oocytes for 30 min (within the time-course of linear uptake) in standard Na+, low-Na+ or Na+-free media with 10-500 μM L-[1-14C]ascorbic acid (final specific activity ≈0.3 GBq/mmol). Oocytes were solubilized with 10% SDS and carbon-14 content measured by liquid scintillation counting. A two-microelectrode voltage-clamp was used to measure currents associated with SVCT1 expressed in oocytes. Oocytes were superfused at 22° C. in standard Na+ medium and clamped at −50 mV. Current was continuously monitored by sampling at 1 Hz. Test solutions were always washed out with substrate-free, Na+-free medium at pH 7.5 for several minutes. Once again, saturation kinetics data were fit to a modified Hill equation in which I and Imax were replaced by uptake V and maximal velocity Vmax for analysis of radiotracer uptake data.

[0076] Chromosome mapping of the SLC23A2 gene encoding human SVCT1—The SLC23A2 gene, which encodes human SVCT1, was mapped using fluorescence in situ hybridization. 1.0 μg of SVCT1 cDNA clone was labeled with digoxigenin-11-dUTP, co-precipitated with 50 μg of tRNA and resuspended in 1×TE at 100 μg/ml. Hybridization of metaphase chromosome preparations from peripheral blood lymphocytes (obtained from a healthy male volunteer) was performed with labeled SVCT1 probe (20 μg/ml) in Hybrisol VI. Digoxigenin-labeling was detected using the Oncor kit, and metaphase chromosomes were counterstained with 4,6-diamidino-2-phenylinode-dihydrochloride (DAPI). The map position of the SLC23A2 gene was determined by visual inspection of the fluorescent signal on the DAPI-stained metaphase chromosomes.

[0077] Fluorescence in situ hybridization with the 2306-bp cDNA probe permitted assignment of the SLC23A2 gene to chromosome 5 in band q31.2-31.3 (FIG. 5). Of 23 metaphases, labeling was detected on the long arm of chromosome 5 in 21 cells, of which 10 displayed labeling on both chromosomes 5. Analysis using the Stanford G3 Radiation Hybrid Panel revealed that SLC23A2 is closely linked to marker D5S500 (LOD score 10.82). A BLAST search based on the full-length SVCT1 sequence identified BAC clone 3049C21, and sequence analysis revealed that BAC3049C21 contains both the 3′ end of SLC23A2 and the 3′ end of MATRIN 3 (a gene encoding a cell matrix protein) in opposing orientation (FIG. 6).

[0078] Northern analysis—Human multiple-tissue Northern blots were probed with the 32P-labeled human EST (SVCT1) probe or with SVCT2 probe (a PCR product corresponding to the first 1 kbp of D87075). The filters were hybridized at 42° C. in 50% formamide, then twice-washed in 5×SSC/0.1% SDS at 50° C. for 30 min and three times in 0.1×SSC/0.1% SDS at 65° C. for 20 min.

[0079] Transport activity associated with SVCT1 expressed in oocytes—Uptake of 500 μM L-[14C]ascorbic acid was stimulated 200-fold and in oocytes expressing SVCT1 (15.5±1.2 pmol/min per oocyte) compared with water-injected control oocytes. With reference to FIG. 6, L-Ascorbic acid uptake followed Michaelis-Menten-type saturation kinetics, with half-maximal concentration (K0.5) of ≈90 μM and Hill coefficient (nH) for L-ascorbic acid close to 1. Uptake was effectively abolished when extracellular Na+ was replaced by choline, indicating that L-ascorbic acid uptake is Na+-dependent (FIG. 6, inset graph), with K0.5 for Na+ of 15-25 mM. It was found that Li+ was unable to substitute for Na+ in driving SVCT1-mediated transport.

[0080] In voltage-clamped oocytes expressing SVCT1, L-ascorbic acid evoked reversible inward currents of up to −150 nA in the presence of extracellular Na+(FIG. 8A), whereas 500 μM L-ascorbic acid evoked currents of only −1±0.5 nA (mean±s.d.) in control oocytes. Oocytes were voltage-clamped at −50 mV in the absence (blank boxes) or presence (hatched boxes) of Na+ at pH 7.5. The oocytes were superfused with 500 μL-ascorbic acid for the periods shown by the solid bar (or additionally 100 μM phloretin, gray box), before washing out with Na+-free, substrate-free medium.

[0081] The currents evoked by 500 μM L-ascorbic acid were pH-sensitive at −50 mV (FIG. 8B). The figure illustrates the pH dependence of the SVCT1-mediated currents (left axis) evoked by 500 μM (filled circle) or 5 mM (open circle) L-ascorbic acid at −50 mV in Na+ medium. The dashed line represents the approximate proportion of L-ascorbic acid present in its deprotonated form (right axis) in the medium, calculated from the Henderson-Hasselbalch equation using pKa1 for L-ascorbic acid of 4.17. Maximum current was obtained at pH 7.5, with a small reduction in current at pH 8.0, but a larger reduction in the current at lower pH. The >60% reduction in current observed at pH 5.5 (compared with pH 7.5) was entirely restored by increasing the L-ascorbic acid concentration to 5 mM. Since over 95% of the L-ascorbic acid (pKa14.2) is present in the deprotonated form at pH 5.5, the significant reduction in transport activity at low pH is not due to the reduction of the effective L-ascorbic acid (1−) species, but rather it is attributable to a reduction in the binding affinity of the transporter for L-ascorbic acid at low pH.

[0082] Substrate selectivity of human SVCT1—No other substrate was found to be as effective in evoking a currrent as was L-ascorbic acid in oocytes expressing SVCT1. FIG. 9 illustrates currents evoked by test substrates (each applied at 500 μM in oocytes clamped at −50 mV) normalized to the L-ascorbic acid-evoked currents in the same oocytes (−114±20 nA, mean±SEM from eight oocytes). The test substrates were dehydroascorbic acid (DHAA); D-isoascorbic acid (IAA); L-ascorbic acid (L-Asc); L-ascorbic acid-2-phosphate (L-Asc2P); L-gulono-γ-lactone (GGL); and D-glucose (D-Glc).

[0083] The K0.5 for L-ascorbic acid (based on evoked currents at −50 mV and at 100 mM Na+) was 54±10 μM (mean±propagated SEM from 5 oocytes). D-isoascorbic acid evoked a current about 15% that of L-ascorbic acid (each at 500 μM). Higher D-isoascorbic acid concentrations evoked currents similar to those for L-ascorbic acid (i.e., these two substrates exhibited similar Imax), but the K0.5 for D-isoascorbic acid (2.7±1.2 mM) was two orders of magnitude higher than that for L-ascorbic acid. Dehydroascorbic acid and L-ascorbic acid-2-phosphate were barely transported. As shown in the inset graph of FIG. 8, the substrate preference of SVCT1 was expressed as the Imax/K0.5 ratios for the first three of these transported compounds, illustrating an exquisite preference for L-ascorbic acid. L-Gulono-γ-lactone (an intermediary metabolite in the synthesis of L-ascorbic acid from D-glucose in animals that can synthesize endogenous L-ascorbic acid) and D-glucose were both excluded. In addition, L-[14C]ascorbic acid uptake was not significantly inhibited by a range of lactic acid, uric acid, succinic acid, oxalic acid, asprin, D-glucose, 2-deoxy-D-glucose, D-mannitol, D-ribose, L-ribose or D-fructose (data not shown). However, L-ascorbic acid-6-palmitate resulted in modest inhibition (20-30%), suggesting that it may be a substrate.

[0084] Phloretin was found to be a potent inhibitor of L-[14C]ascorbic acid uptake (≈80% inhibition, data not shown) and of the L-ascorbic acid-evoked current (FIG. 8A). Phloretin also blocked a Na+“leak” current that could occur in the absence of L-ascorbic acid or other substrate; this was found to be as much as 10% of the L-ascorbic acid-evoked current, proportionately smaller than the Na+ leak pathway found in the rat SVCT1.

[0085] Human SVCT1 is approximately 30% similar (at the amino-acid level) to the mouse yolk-sac permease-like protein mYspl1. mYspl1 was proposed to be a nucleobase transporter on the basis of weak sequence homology with prokaryotic nucleobase transporters (Guimarães et al., Development 121:3335-3346 (1995)). A range of nucleobases, nucleosides and nucleoties were therefore included in the search for additional substrates for SVCT1. Nonetheless, of the nucleobases (adenine, thymine, uracil), nucleosides (adenosine, 2-deoxyadenosine, uridine, guanosine, inosine), ribonucleotides (AMP, ADP, ATP, GTP, UTP) and deoxyribonucleotides (dATP, dGTP, dCTP, dTTP) we tested, none resulted in any significant inhibition of L-[14C]ascorbic acid uptake in oocytes expressing SVCT1.

[0086] Identification of transport activity for human SVCT2—When expressed in oocytes, SVCT2 resulted in a 15-fold stimulation of L-[14C]ascorbic acid uptake (1.2±0.1 pmol/min per oocyte) compared with control oocytes. Like SVCT1, SVCT2-mediated L-[14C]ascorbic acid transport was saturable, with K0.5 of 65 μM (FIG. 10), and 94% Na+-dependent (FIG. 10, inset graph). Among a range of potential inhibitors tested, only saturating L-ascorbic acid inhibited the uptake of 100 μM L-[14C]ascorbic acid. (The low SVCT2 expression levels in oocytes precluded detailed voltage-clamp analysis as performed for rat SVCT2.) Replacement of sodium ion by choline abolishes transport, confirming that SVCT2 is Na+-coupled.

[0087] Tissue distribution of human SVCT1 and SVCT2—The tissue distribution of SVCT1 and SVCT2 was determined by Northern blot analysis of human tissues under high stringency conditions. Probing for SVCT1, transcripts of about 3 kb were detected in kidney, liver, small intestine, colon, ovary and prostate, with a weaker signal in pancreas. A transcript in thymus of around 9 kb may result from alternative splicing or may correspond to a closely-related gene product distinct from SVCT2. A 7.5-kb transcript was detected in most tissues probed for SVCT2, including brain, spleen, prostate, testis, ovary, placenta, and peripheral blood leukocytes.

[0088] Based on a survey of the frequency and tissue sources of closely-related EST clones, it is possible to predicte additional tissues in which SVCT1 and SVCT2 may be expressed. These are shown in the following table:

	TABLE 1
	Human	Mouse
	SVCT1	SVCT2	SVCT1	SVCT2
Tissue
Brain		4A
Retina		15B
Pineal gland		1C
Adipose tissue (white)		1D
Skin (melanocyte)		4E
Lymph node				2F
Germinal center B cells	1G
T cell		1H	2I
Mammary gland				5J
Uterus (during pregnancy)		5K
Human tumors
Kidney	2L
Uterus	1M
Prostatic neoplasia	1N
Parathyroid tumor		5O
Anaplastic oligodendroglioma		2P
Glioblastoma		1Q
Gessler Wilms tumor		1R
Pooled germ cell tumors		2S
Ovary		1T
Corresponding EST database accession numbers are:
AAA322234, AA323329, AA323374, AA984438;
BH01519, H01625, R81499, R81742, T53720, T54313, W28570, W28623, AA000999, AA001558, AA012920, AA013005, AA013480, AA015699, AA021020;
CAA364385;
DAA302691;
EH99366, N23756, N32463, N32511;
FAA185385, AA210597;
GAA811090;
HA352785;
IAA097984, AI550622;
JAA472304, AA821651, AA9801311, AI465994, AI606903;
KAA028023, AA028024, AA085766, AA128373, AI095660;
LAI334656;
MAI367693;
NAA604857;
OAA782627, AA854872, AI040896, AI056144, AI078653;
PAI497603, AI582791;
QAI056441;
RAA665698;
SAA655944, AI206350;
TAA075501.

[0089] Identification of SVCT1-related EST clones was limited to B lymphocytes of the germinal center as well as certain tumor cell types. However, numerous SVCT2-related EST clones were detected in several other tissues, suggesting that SVCT2 may also be expressed in pineal gland, retina, adipose tissue, skin, activated T-lymphocytes and uterus. Murine SVCT2 may also be expressed in mammary gland and lymph nodes.

[0090] 3. Therapeutic Applications

[0091] Therapeutic applications involving modulation of the activity of vitamin C transporters include:

[0092] Cancer: It is well known that oxidative stress is a critical factor in cancer development. In some cancers, such as brain tumors, the cancer cells accumulate vitamin C as a free-radical scavenger to avoid damage by oxidative stress. Elevated levels of Vitamin C are also seen in lymphocytes of leukemia patients. Therefore, inhibition of the vitamin C transporters described herein may lead cancer therapies and preventative measures.

[0093] Brain tumors: In gliomas (i.e., astrocyte tumors, the most common brain tumors) oxidative stress is pronounced due to anaerobic glycolysis, and vitamin C accumulates to protect these cells. Vitamin C accumulation probably occurs through upregulation of SVCT2 in those cells. Therefore, inhibition of SVCT2 may lead to a therapeutic strategy to treat brain tumors and probably also other tumors.

[0094] Leukemia: Assignment of the gene encoding SVCT2 to the long arm of human chromosome 5, at band 5q31.2-31.3, within a region that is commonly deleted in malignant myeloid diseases raises the possibility that SVCT1 may play a role in tumor suppression. Indeed, in addition to its accepted role in antioxidation, there is growing interest in the potential use of L-ascorbic acid as an anticancer agent, a concept strengthened by the finding that this compound acid has a cytotoxic effect on leukemia cells in vitro.

[0095] Ischemia/stroke: In response to the anoxic state which occurs during ischemia, vitamin C is released from neurons to the extracellular space. As a consequence, when reoxygenation occurs following ischemia, free radicals will accumulate because the supply of intracellular vitamin C is no longer sufficient to scavenge the radicals. It is thought that people with enhanced brain vitamin C content enjoy improved protection against ischemia. Therefore, increased delivery of vitamin C by upregulation of the transporter proteins disclosed herein (i.e., increased transport across the choroid plexus and capillary endothelial cells, and/or increased absorption by the neurons) may represent an important therapeutic application.

[0096] During ischemia, there occurs a depletion of energy supply and a run-down of electrochemical ion gradients in neuronal cell membranes, which may result in reversed vitamin C transport (neuronal exit) by SVCT2. Depletion of vitamin C from neurons may exacerbate oxidative damage during the reoxygenation phase.

[0097] Eye: Increased accumulation of vitamin C by SVCT2 and SVCT1 in the cornea and tear fluid, respectively, protects the eye from damage due to ultraviolet radiation and oxidative stress. Studies indicate that both excessive and insufficient delivery of vitamin C to the eye lens may promote cataract formation. Therefore, depending on the situation, either inhibition or upregulation of SVCTs may be beneficial.

[0098] Vitamin C and dehydro-L-ascorbic acid (DHAA) cycling: Oxidation of vitamin C (e.g., as a result of scavenging of free radicals during oxidative stress), results in the formation of DHAA, which is toxic. Therefore, DHAA is kept at very low concentraion in normal human plasma. Certain cells such as astrocytes, lymphocytes, neutrophils and erythrocytes preferentially take up DHAA through facilitated glucose transporters of the GLUT-type. Once inside the cell, DHAA is reduced to vitamin C (either by direct chemical action of glutathione or by an enzymatic process that employs glutathinone and NADPH as reducing factors), and vitamin C is then released. In the brain, astrocytes regenerate vitamin C oxidized to DHAA due to neuronal activity, and return it back to neurons. In pathological situations, excessive oxidative stress may exceed the capacity of neurons and other cell types to regenerate oxidized vitamin C, which may lead to accumulation of toxic levels of DHAA.

[0099] Diabetes: SVCT2 is strongly expressed in the pancreas. Oxidative stress leads to accumulation of DHAA. Structurally, DHAA is similar to the diabetogenic agent alloxan, which destroys the pancreatic beta cells that produce insulin. Inhibition of SVCT2 specifically in the pancreas may limit DHM formation in the pancreas of diabetics and may help to protect the beta cells. Thus, therapeutic interventions of vitamin C transport and metabolism may lead to new treatment strategies for patients with diabetes.

[0100] Vitamin C in blood vessels and heart disease: Blood vessels require vitamin C in order to remain healthy. The vascular endothelium plays a key role in the local regulation of vascular tone by release of vasodilator substances such as nitric oxide (NO) and vasoconstrictor substances (i.e., thromboxane A2 and free radicals). NO plays an important role in basal and stimulated control of vascular tone in coronary arteries and coronary microcirculation, and regulation is altered by risk factors such as hypercholesterolemia, chronic smoking and hypertension. Endothelial dysfunction can cause myocardial ischemia and may be in part reversible by antioxidants such as vitamin C. Endothelial cells take up vitamin C in a sodium-dependent manner, possibly via SVCT2. Defective vitamin C metabolism in the vascular endothelium also leads to capillary fragility. Thus, therapeutic upregulation of SVCT2 in endothelial cells may be beneficial.

[0101] Therapeutic alteration of vitamin C homeostasis: Since plasma vitamin C is controlled at a fairly constant level (10-160 μM), whereas its concentration is at least 100 times higher in tissues (e.g., adrenal gland, thymus corpus luteum, retina, cornea) that depend on the vitamin, dietary vitamin C supplementation is probably not very effective in augmenting the cellular effects described above; this may explain the continuing controversy regarding the protective action of this vitamin in connection with the various noted pathologies. However, the ability to upregulate vitamin C transporters in specific tissues and cell types may allow a more effective increase in the supply of the vitamin to target tissues. Thus, this approach may lead to unique, highly promising and novel therapeutic applications.

[0102] Vitamin C levels inside the brain are under tight control and are compartmentalized. Vitamin C is delivered to the brain via SVCT2 in the choroid plexus and via the capillaries of the blood-brain barrier, which may also express SVCT2. Vitamin C enters neurons via SVCT2 which accumulate it at very high levels (up to 10 mM) for protection against reactive oxygen species produced during neuronal activity. Under normal conditions, asctrocytes accumulate vitamin C at much lower levels than neurons (˜1 mM in astrocytes). Total brain tissue vitamin C levels are under hormonal control (i.e., regulation by circulating estrogen). Possibly, estrogen may directly affect the expression of SVCT2. Vitamin C levels in the brain also exhibit marked circadian patterns and variations are closely related to motor behavior through activation of certain glutamatergic pathways. This suggests novel therapeutic approaches for the treatment of insomnia and alteration of alertness. Vitamin C also acts as a neuromodulator of glutamatergic and dopaminergic neurotransmission. It is furthermore a co-factor in the synthesis of noradrenaline and many neuropeptides.

[0103] Therapeutic inhibitors and activators: As described above, phloretin has been demonstrated to inhibit SVCT1 and SVCT2.

[0104] Drug transport: Transport of drugs across epithelial barriers can be accomplished by linking a drug to a species transported by SVCT1 or SVCT2, thereby facilitating transport of the drug into cells expressing the transporter. For example, since the transporter SVCT1 is expressed in intestinal enterocytes, this strategy can be employed to facilitate oral administration of the drug. The drug linked to the transported species is absorbed intact into enterocytes, whereupon native enzymes inside the enterocyte or, following basolateral exit, in the blood or liver, cleave the drug from the transported species. Drugs that have proven amenable to an analogous approach using the intestinal peptide transporter PepT1 are acyclovir, the anti-viral, anti-herpes agent, and L-α-methyl-DOPA.

[0105] More specifically, drugs (possibly including antiviral drugs such as acyclovir) may be linked to L-ascorbic acid via ester-linkage, e.g., to the C5 or C6 hydroxyl group. Studies have shown that monosaccharide-conjugated drugs (such as acetaminophen) can be transported via the sodium glucose transporter SGLT1 in small intestine if the drugs are attached through and ether linkage to the C-1 of glucose, and that SGLT1 has spare space in its translocation pocket which can accommodate drugs if attached in the correct configuration; see Awazu et al. Biochim. Biophys. Acta 1381:340-346 (1998).

[0106] An important pathway for the metabolism of xenobiotics and cleavage of ester-linked prodrugs is catalyzed by the carboxylesterases, a family of enzymes that is involved in hydrolysis of chemical compounds, generally leading to detoxification. Several esterases have been purified, cloned, and characterized. Two forms, hydrolase A and hydrolase B, are present in liver microsomes in a number of species, including humans. These are also detected in extra-hepatic tissues. A third esterase, hydrolase S, is found in liver microsomes and serum, and may be a serum carboxylesterase secreted from the liver. See Yan et al., J. Biol. Chem. 270(32):19128-34 (1995). Thus, cleavage of these prodrug ester linkages may primarily occur in liver and blood, and not in epithelial cells of the intestine (enterocytes).

[0107] However, prodrugs may also include peptide bonds or ether linkage instead of ester bonds between the drug and the transported species. Peptide bonds may be hydrolized by specific peptidases that exist inside enterocytes.

[0108] Female infertility: It has been known for some time that vitamin C is essential for female fertility. Recent data has shown that vitamin C accumulates in maturing oocytes to high levels, and that this accumulation is compromised with aging. It is thought that the vitamin serves as a key anti-oxidant in eggs and early embryos. In women, a large component of the age-dependent loss of fertility is due to egg-dependent anomalies. In in vitro animal models, reactive oxygen species can create eggs of abnormal quality, similar to that seen in some infertile women, and infertility in some women may be due to inadequate levels of the antioxidant ascorbic acid. Understanding how eggs take up ascorbic acid and maintain their levels will facilitate understand this clinically relevant topic. Recent in situ hybridization data demonstrates that SVCT2 mRNA is strongly expressed in the rat ovary, in particular in thecal cells, granulosa cells, luteal cells and oocytes. SVCT2 expressed in the plasma membrane of these cells may play an important role in providing oocyte with appropriate supply of vitamin C. Similar to the adrenal medulla, SVCT2 also appears to be present in steroid producing cells of the ovary, i.e., thecal and luteal cells, where the vitamin C may be required as a cofactor for enzymatic reactions.

[0109] In addition, SVCT1 mRNA was also detected in the ovary where it may have similar funcitons as SVCT2. However, its cellular distribution in the ovary has not yet been determined.

[0110] Although the present invention has been described with reference to specific details, it is not intended that such details should be regarded as limitations upon the scope of the invention, except as and to the extent that they are included in the accompanying claims.

Claims

9. A method of transporting vitamin C across a membrane, the method comprising the steps of: a. causing expression of a protein encoded by a nucleic acid comprising SEQ ID NO: 2, or substitutions or modifications thereof, wherein the substituted protein transports vitamin C across membranes; b. causing integration of the protein within a membrane; and c. contacting the membrane, under conditions favoring vitamin C transport, with vitamin C, thereby resulting in transmembrane transport of vitamin C.

31. The method of claim 9, wherein the membrane comprises a lipid bilayer.

32. The method of claim 9, wherein the protein is integrated by transforming a cell with the nucleic acid, thereby causing expression of the protein within the cell and integration of the protein in a membrane of the cell.

33. The method of claim 9, wherein the nucleic acid corresponds at least to conserved regions of the sequence of SEQ ID NO: 2.

34. The method of claim 32, wherein the cell is transformed by transfection with the nucleic acid.

35. The method of claim 32, wherein the cell is derived from kidney, uterus, liver, brain, ovary, skin, endocrine, exocrine, retina, pineal gland, adipose, mammary gland, lymph node, brain, or intestine tissue.

36. The method of claim 32, wherein the cell is a neuron, astrocyte, cancer cell, epithelial cell, enterocyte, colon cell, prostate cell, endothelial cell, neuroendocrine cell, corneal epithelial cell, pigmented ciliary epithelial cell, T cell, melanocyte, or osteoblast.