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INVITED REVIEW
Department of Cell Biology, Institute of Anatomy, University of Aarhus, Aarhus, Denmark
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ABSTRACT |
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 TOP ABSTRACT FOLATEVITAMIN B12FOLATE, VITAMIN B12, AND...CONCLUSIONS AND FUTURE...GRANTSREFERENCES |
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megalin; cubilin; folate-binding protein; proximal tubule; endocytosis
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FOLATE |
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TOPABSTRACTFOLATEVITAMIN B12FOLATE, VITAMIN B12, AND...CONCLUSIONS AND FUTURE...GRANTSREFERENCES |
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0.1 nM, suggesting that serum FBP is fully saturated. The amount of folate associated with serum proteins has been estimated to be 20% in rats within a wide serum folate concentration range (127). In humans, the fraction of protein-bound folate has been estimated to be from 20 (156) to 65%, being constant within a wide concentration range. |
VITAMIN B12 |
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TOPABSTRACTFOLATEVITAMIN B12FOLATE, VITAMIN B12, AND...CONCLUSIONS AND FUTURE...GRANTSREFERENCES |
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2–3 mg, with 1–1.5 mg in the liver, classically considered the major organ for B12 accumulation (1, 45). Mammals are unable to synthesize vitamin B12 and thus rely on dietary intake; however, they are able to convert the different forms of vitamin B12 into the active forms, methylcobalamin and 5-deoxyadenosylcobalamin. Vitamin B12 is synthesized by microorganisms, particularly in the gastrointestinal tract of herbivorous animals, and absorbed. Thus the major food sources of the vitamin are liver, meat, fish, dairy products, eggs, and shellfish.
After ingestion, vitamin B12 is released from dietary protein by the acidic environment and peptic digestion in the stomach, followed by binding to haptocorrin (HC), a 65-kDa glycoprotein secreted in saliva and gastric juice and favored by the acidic environment. In the duodenum, pancreatic secretion raises intraluminal pH and facilitates degradation of HC by pancreatic proteases, causing vitamin B12 to bind to intrinsic factor (IF; molecular mass 50 kDa) secreted by the parietal cells of the gastric mucosa and by the pancreas (125). The IF-B12 complex is absorbed in the ileum by binding to the intestinal IF-B12 receptor, the cubilin-amnionless (AMN) complex (40, 126). The binding to the receptor depends on B12 binding to IF (11). Following absorption, B12 is released from IF within the enterocyte (113). In serum, B12 is bound to transcobalamin (TC), a 45-kDa nonglycosylated serum protein, and HC. Normal B12 concentration in human serum is estimated to be 0.3 nM (102) compared with 1.1 nM in normally fed laboratory rats (7). The concentration of TC in normal human serum is 1 nM, of which 10% is saturated, depending on vitamin intake (15), whereas the concentration of HC is 0.4 nM (93), of which 75% is saturated (101). Thus normally no free B12 is present in the circulation. Although TC binds only 25% of the circulating vitamin, it is responsible for the delivery of B12 to most tissues. Indeed, whereas inherited TC deficiency is associated with severe megaloblastic anemia, patients with HC deficiency may be asymptomatic with normal levels of MMA despite low total serum B12 (110). This is also reflected in the half-life of the two carrier proteins, being <2 h for TC compared with several days for HC. HC binds to the asialoglycoprotein receptor, and in adults it is probably only taken up in significant amounts in the liver (24). The function of HC in adults is not fully understood, although a role in the clearance of cobalamin analogs from the circulation has been suggested (39). Vitamin B12 is a highly conserved vitamin, and the daily losses in humans is estimated to be 0.1–0.2% of total body content (1). The highest losses occur through feces, and B12 is secreted in bile, although to a large extent reabsorbed when supported by sufficient secretion of IF and a functional ileal-absorptive apparatus (48).
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FOLATE, VITAMIN B12, AND THE KIDNEY |
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TOPABSTRACTFOLATEVITAMIN B12FOLATE, VITAMIN B12, AND...CONCLUSIONS AND FUTURE...GRANTSREFERENCES |
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Glomerular Filtration of Vitamins and Carrier Proteins
The molecular mass of folate (440 Da) suggests that free folate is freely filtered in the glomeruli. Due to the association of folate with serum proteins, the filtration of folate in humans is estimated to be 50–65% of that of inulin (46), suggesting a filtered load of free folate of 1 mg/24 h in humans (127). A small fraction of folate is bound to serum FBP. The molecular mass of 35 kDa suggests that this protein to a large extent is filtered, and FBP has been detected in human urine at a concentration of 0.5–4 nM (50). Most protein-bound folate in serum is loosely associated with albumin (132). The fraction of filtered albumin is traditionally considered to be low; however, recent evidence has suggested that a much larger amount is filtered in the normal kidney (117), although this is yet to be established.
The glomerular filtration of vitamin B12 similarly is dependent on serum protein binding and thus on the concentration of B12 in serum. In humans, no urinary excretion of B12 was detected at concentrations <1.1 ng/ml (
800 pM), whereas at concentrations >12 ng/ml (8 nM) B12 is excreted at a rate similar to the glomerular filtration rate (147). Thus unbound B12 is freely filtered and may in fact serve as a marker to estimate glomerular filtration rate (99). At normal serum B12 concentration, the filtered load of the vitamin in humans has been estimated to be 1.5 µg (79). The molecular mass of TC suggests that the TC-B12 complex is filtered, supported by the demonstration of small amounts of B12-binding proteins, including TC, in human urine (13, 79, 143). Most circulating HC, originating from myeloid cells, is heavily glycosylated (39), probably limiting filtration of this protein, and the origin of urinary HC remains to be established.
Renal Tubular Reabsorption of Filtered Vitamin and Carrier Proteins
The major pathway for the uptake of filtered macromolecules in the proximal tubules is by receptor-mediated endocytosis. This involves the specific binding of a ligand to a receptor in the apical plasma membrane. The receptor-ligand complex is internalized by invagination of the plasma membrane caused by adaptor molecule-mediated formation of a cytoplasmic clathrin coat (122). Internalization is followed by dissociation of the invaginations from the plasma membrane, forming vesicles. While the coat detaches, vesicles may fuse with other newly formed vesicles, or with an existing pool of larger vesicles, followed by acidification of the intravesicular lumen and the dissociation of the ligand from the receptor. The ligand may be further transported into lysosomes for degradation, or possibly storage, or into the cytosol for further processing/transport. The receptor is recycled back to the luminal membranes through a recycling compartment; however, it may also be transported to lysosomes for degradation. In addition to the formation of a clathrin coat, other mechanisms of internalization have been established, including noncoated endocytosis and internalization by caveolae involving the protein caveolin (63). It has been proposed that glycosylphosphatidylinositol (GPI)-anchored proteins may by internalized by caveolae rather than by clathrin-coated pits (3).
Several different receptors mediating endocytosis of filtered ligands have been identified in the kidney proximal tubule cell (reviewed in Ref. 28). The receptors, megalin and cubilin, and the folate receptor (FR) have been implicated in the uptake of folate, vitamin B12, and their carrier proteins. The structure, renal expression, regulation, and mutual interaction of these receptors will be reviewed, followed by a discussion of their possible role in the renal handling of B12 and folate.
Megalin.
Megalin is a multifunctional, endocytic receptor binding a number of structurally and functionally different ligands (Table 1). Ligands for megalin that may be filtered in the glomeruli include vitamin D-binding protein (DBP), retinol-binding protein (RBP), TC-B12, FBP, parathyroid hormone, insulin, epidermal growth factor (EGF), prolactin, albumin, hemoglobin, myoglobin, 
2- and 
1-microglobulin, apolipoprotein H, lysozyme, cytochrome c, and -amylase.
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40% of all Ca2+-binding activity in the renal cortex (30). The ligand-binding type A repeats are negatively charged Ca2+-binding protein domains, and Ca2+ is important for most ligand binding to megalin. An important role of megalin in Ca2+ metabolism has also been proposed (27, 57, 151). Site-directed mutations of basic amino acid residues in aprotinin, a 6-kDa proteinase inhibitor and a ligand for megalin, decrease the affinity for the receptor, suggesting that binding is charge dependent and favored by cationic sites on the ligands (91). However, many ligands are anionic proteins, indicating that the distribution of charge rather than the overall isoelectric point is important for binding.
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Much of our knowledge on the functions of megalin is based on data recovered from the study of megalin-deficient mice. These mice, produced by gene targeting, exhibit severe forebrain abnormalities as well as lung defects (150). Most of them die perinatally; however, some survive to adulthood, constituting a model for the study of megalin function. Additional evidence has been recovered from mice with targeted kidney-specific knockout of the megalin gene (77). Megalin-deficient proximal tubule cells are characterized by a loss of endocytic invaginations, vesicles, and the membrane-recycling compartment, dense apical tubules (DAT) (31). So far, no significant changes in transport of water, electrolytes, glucose, or amino acids have been described in megalin-deficient mice; however, an increased amount of a number of low-molecular-weight serum proteins has been identified in urine. Analyses of megalin knockout mice and patients with low-molecular-weight tubular proteinuria, including Dent's disease, have shown several analogies (78, 105).
Little is known about the regulation of megalin gene expression in vivo; however, receptor-associated protein (RAP), a 45-kDa protein modulating posttranslation protein processing (22, 23, 149, 152) and shown to bind megalin (30) as well as other members of the LDL-receptor family, is required for normal expression and subcellular distribution of megalin in kidney proximal tubules (12). RAP inhibits binding of almost all ligands to megalin, constituting an important tool for the study of megalin function. A HNEL endoplasmic reticulum (ER) retention signal has been identified in RAP (22) targeting it mainly to the ER, where it recycles between the ER and the cis-Golgi (22). RAP serves as a chaperone protecting newly synthesized LRP from the early binding of ligands, which are also synthesized by the cells (Fig. 5) (22, 23, 149, 152). Such premature binding of ligands within the ER may cause receptor aggregation and retention. In addition, RAP may be involved in folding of the receptors (Fig. 5) (23). RAP deficiency is associated with a reduction in megalin expression to 25% of normal and a change in subcellular distribution, causing a reduction in brush-border expression and an accumulation of megalin in intracellular compartments including the ER and the paramembranous ER (12). This strongly suggests that RAP serves a similar chaperone function for megalin. RAP-deficient mice are viable and fertile with no overt abnormalities in renal function (149). In contrast to megalin-deficient proximal tubule cells, no changes in the ultrastructural appearance of the endocytic apparatus were observed in RAP-deficient mouse kidneys (12). Detailed analysis including two-dimensional gel electrophoresis showed increased urinary excretion of specific proteins, including DBP and -amylase (12). Thus RAP-deficient mice, having a 75% reduction in megalin expression, exhibit low-molecular-weight proteinuria and have been used to study megalin function in vivo.
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STRUCTURE.
Cubilin was originally identified as the target of teratogenic antibodies in rats (Fig. 2). It is a 460-kDa protein with little structural homology to other known endocytic receptors (Fig. 3) (72, 92). Cubilin has no transmembrane domain, and it can be released from renal cortical membranes by nonenzymatic and nonsolubilizing procedures (92). It is composed of a NH2-terminal 110-amino acid region necessary for membrane anchoring of the receptor (74) followed by eight EGF-like repeats and 27 complement subcomponents C1r/C1s, Uegf, and bone morphogenic protein-1 (CUB) domains. The structure of the CUB domains has been studied in spermadhesin. They are organized as barrel-like structures containing two, five-stranded -sheets connected by surface-exposed -turns (115), which may be arranged so that the less-conserved surface of the -turns is externally exposed for ligand binding. The many CUB domains in cubilin support the ability of the receptor to bind a variety of ligands. Binding sites for selected ligands have been partially localized. A binding site for IF-B12 has been located within CUB domains 5–8, whereas the binding site for RAP has been located within CUB domains 13–14 (74). Other studies have suggested additional IF-B12 as well as albumin binding sites in a 113-residue NH2 terminus, (155). Although IF-B12 inhibits binding of albumin to cubilin, the binding sites for the two proteins do not appear to be identical within this domain (155). Finally, megalin appears to bind to the NH2-terminal region including CUB domains 1 and 2 (154). The NH2-terminal region contains a furin-cleavage site, a potential cysteine palmitoylation site, and a putative amphipathic helix structure similar to the lipid-binding regions of apolipoproteins (74).
RENAL EXPRESSION.
Cubilin is highly expressed in the renal proximal tubule (Fig. 4) (119). As with megalin, immunoreactive cubilin can also be identified in lysosomes (126). Although the extrarenal expression of cubilin seems more restricted than megalin, the two receptors are coexpressed in a number of epithelia, including the ileum and the rodent yolk sac (27).
Normal expression of cubilin is dependent on AMN, a 45-kDa transmembrane protein (Fig. 3) identified as an important factor for the normal development of the middle portion of the primitive streak in mice (65). Previously, a 40- to 45-kDa protein of unknown nature was shown to coelute with cubilin when purified from kidney by IF-affnity chromatography (11). Later studies suggested this protein to be AMN (40). Cubilin and AMN colocalize in kidney proximal tubule. Cotransfection of cubilin fragments and AMN into Chinese hamster ovarian (CHO) and Madin-Darby canine kidney cells shows that AMN interacts with the EGF-type repeats of cubilin and is essential for normal translocation of the cubilin-AMN complex from the ER to the plasma membrane and for the subsequent endocytosis (34, 40). Furthermore, dogs with a mutation in the AMN gene (52, 53) as well as AMN-deficient mouse epithelial cells reveal defective apical insertion of cubilin (6, 41, 136). Mutations in either the cubilin or the AMN gene have been identified in Imerslund-Gräsbeck disease (2, 138), a rare inherited vitamin B12 deficiency syndrome characterized by defective intestinal absorption of IF-B12 (21, 144) and an apparent geographical concentration in Scandinavia and the Middle East (139). Cubilin gene mutations were identified in Finnish and Arab families (2, 139). In two Finnish families, this involved either a one-amino acid substitution in CUB domain 8 affecting the binding of IF-B12 or a point mutation expected to activate a cryptic intronic splice site causing an in-frame insertion with several stop codons, predicting a truncation of the receptor in CUB domain 6 (2, 73). Whereas the patient with the latter mutation has overt proteinuria, patients with amino acid substitution reveal varying degrees of proteinuria ranging from little or no, to clear-cut (144). Affected members of three Norwegian families, shown to have a nucleotide deletion causing the introduction of an early stop codon in the AMN gene (138), were all previously characterized and had proteinuria at the time of diagnosis. Other mutations have been identified in the AMN gene; however, the renal phenotype of these patients is not clear (139). Based on the variety of mutations shown to cause Imerslund-Gräsbeck syndrome, it may by hypothesized that the difference in renal phenotype, in particular the degree and type of proteinuria, reflects the degree of inactivation of cubilin function, in particular whether the mutation affects the multiligand properties or only the IF-B12-binding site.
Like megalin, cubilin binds RAP (11); however, the function of RAP binding to cubilin remains unclear. Unpublished observations in our laboratory showed that the expression of cubilin was reduced in RAP-deficient mice, somewhat similar to the changes in megalin expression, showing decreased overall expression to 25% of controls. In addition, increased amounts of proteins (up to 140 kDa) reactive with anti-cubilin antibodies were observed in the urine of RAP-deficient mice. Whether this was due to a direct role of RAP in the expression of cubilin, or reflects the reduced expression of megalin, remains to be established.
FRs. FRs are membrane-anchored proteins binding folate with high affinity. They were originally identified as a soluble FBP in milk (Fig. 2) (44), and later their presence was established in both serum and tissues (4, 54). The term folate receptor has been introduced to indicate its function in cellular folate uptake (4).
STRUCTURE.
FRs are glycosylated 40-kDa proteins binding folate with high affinity (Kd 1 nM) (4, 54, 67). At least four FR isoforms have been identified and characterized in humans. FR and FR are membrane-associated, GPI-linked proteins (Fig. 3) (75, 141) expressing different affinities for different stereospecific folate analogs (145). They may be enzymatically released from the membranes (38, 75, 82). FR
is specific for hematopoietic cells and present in serum (130). The fourth human FR gene (FR
) predicts a 27.7-kDa protein with a unique expression pattern in both adult and embryonic tissues (133). Whereas at neutral pH FRs bind most naturally occurring folates, dissociation is rapid at low pH. Binding of folate to the FR induces conformational changes, increasing stability and decreasing hydrophobicity of milk FBP (64).
RENAL EXPRESSION.
FRs are heavily expressed in kidney proximal tubule brush-border membranes (Fig. 4) (9, 58, 59, 66, 129) and have been identified in the mouse glomerulus (14) and in human urine (50). Immunocytochemical studies have localized the FR to the proximal tubule brush border, endocytic invaginations, including coated pits, endocytic vesicles, and DAT (9, 58). Identification of mRNA suggests that the adult human kidney expresses both FR and FR (116). In addition to the kidney, FR is present in other, predominantly epithelial, cells, whereas FR is expressed at low to moderate levels in several different tissues (4, 54, 75, 116).
Targeted gene knockout of folbp1 and folbp2 (the mouse equivalents to FR and FR) has confirmed a role of the FR in folate metabolism (107) and renal folate transport (10). Deletion of folbp1 is lethal and associated with changes in serum folate and embryonic defects that can be rescued by supplementing the dams with folate (107, 134).
The expression of FRs is regulated by extracellular folate concentration. In vitro studies suggest that FRs are upregulated when cells are grown under low-folate conditions (55, 68), whereas in the kidney FRs are downregulated in mice and rats fed a low-folate diet (35, 43).
Interaction among megalin, cubilin, and FBP. A metabolic interaction between folate and B12 is well established. Recent studies have indicated additional interaction between proteins involved in the uptake of these vitamins, showing binding of both cubilin and FBP to megalin. A high-affinity, Ca2+-dependent, and partially RAP-inhibitable binding between megalin and cubilin has been demonstrated in vitro (92). Megalin deficiency is associated with reduced brush-border expression of cubilin (6), and in megalin-deficient mice the cubilin ligand transferrin is accumulated at the proximal tubule luminal membranes, revealing defective uptake (71). Also, the uptake of another cubilin ligand, HDL, is inhibited in vitro by anti-megalin antibodies as well as by megalin anti-sense oligonucleotides (49). This indicates that megalin may mediate the cointernalization and possibly recycling of cubilin. In addition, megalin and cubilin share a number of ligands, including DBP, immunoglobulin light chains, albumin, and RAP (Table 1). Thus in epithelia coexpressing megalin and cubilin, including kidney proximal tubule, megalin and cubilin appear to act in concert, mediating endocytosis of the same ligands. Megalin also binds milk FBP (14), providing a mechanism for the uptake of FBP-bound folate. Soluble milk FBP structurally resembles GPI-linked FRs (60, 81) coexpressed with megalin in the luminal plasma membranes of kidney proximal tubule and other epithelia, i.e., the choroid plexus and yolk sac (28). No direct interaction between megalin and GPI-linked FRs in the plasma membrane has been demonstrated; however, it has previously been shown that the related LRP mediates internalization of the GPI-anchored urokinase receptor (33), indicating that a similar interaction between megalin and FR is possible. This may lead to the hypothesis that megalin is involved in intracellular translocation of FRs, possibly regulating luminal expression of membrane FR by internalization and degradation.
Proximal Tubule Uptake of Folate and Vitamin B12
Proximal tubule uptakes of both folate and vitamin B12 were recognized early and shown to be saturable processes (46). At physiological serum concentrations, the estimated amounts of vitamins filtered in the glomeruli exceed the recommended daily intake, whereas the urinary excretion of both intact folate and vitamin B12 is minimal. Thus proximal tubule receptor-mediated uptake efficiently prevents urinary losses. Recent studies have provided significant information on the molecular mechanisms responsible for this, involving the endocytic receptors presented above.
Vitamin B12.
Megalin is essential for the proximal tubule reabsorption of filtered TC-B12 (13), mediating endocytosis of TC-B12 (90, 104). Megalin and TC colocalize within the endocytic apparatus of rabbit kidney proximal tubule cells (142). TC-B12 binds to megalin with an estimated affinity (Kd) of 183 nM when analyzed by surface plasmon resonance (SPR) analysis, also showing a possible second binding site (Kd 1.4 µM). Binding to immobilized megalin in microtiter trays revealed a half-maximum binding of 12.5 nM, indicating that the affinity may be higher than estimated by SPR analysis. The importance of megalin for the tubular reabsorption and renal accumulation of TC-B12 was established using megalin knockout mice (13). These revealed increased urinary excretion of B12 and a 28-fold increase in renal B12 clearance, along with a 4-fold decrease in the B12 content of megalin-deficient mice kidneys. Immunocytochemistry in wild-type mice showed that most of the reabsorbed vitamin was located in the very early part of the proximal tubule, indicating efficient reabsorption (13).
An additional 62-kDa TC-B12 receptor has been identified in the kidney and other tissues, including placenta, liver, and intestine (16–18). This receptor is a glycosylated 45-kDa single polypeptide with a yet unknown primary structure. It is normally present as a 124-kDa dimer in both apical and basolateral membranes of kidney proximal tubule, however, with a 90% distribution to the basolateral membranes when estimated by membrane fractionation (17, 18). The expression appears to be regulated by corticoids (17). Its role in TC-B12 uptake is supported by the low tissue B12 and apparent vitamin B12 deficiency developing in rabbits following injection with an antiserum against this receptor (16) and by the decrease in renal uptake of orally administered labeled B12 in adrenalectomized rats (17). It was recently suggested that this ubiquitous TC-B12 receptor binds to megalin and that this binding is associated with increased binding of TC-B12 to the purified receptors (153). It was also shown that the immunization of rabbits with megalin was associated with decreased expression of the TC-B12 receptor in purified apical kidney membranes, leading to the suggestion that megalin is involved in the apical targeting of this receptor. This proposed functional and structural interaction between megalin and the 62-kDa TC-B12 receptor awaits further clarification. Evidence suggests that the major mechanism for renal accumulation of vitamin B12 is by tubular reabsorption of filtered TC-B12. Thus the 10–90% distribution of the 62-kDa TC-B12 receptor in apical vs. basolateral renal membranes is puzzling; however, it may suggest an alternative role for the 62-kDa receptor in the kidney, e.g., in basolateral uptake or secretion. The distribution of labeled B12 injected during vitamin depletion as well as during vitamin load fits a model of cellular TC-B12 uptake involving two distinct receptors: a possibly regulated ubiquitous TC-B12 receptor mediating saturable cellular uptake, and a luminal renal tubule receptor mediating constitutive high-capacity reabsorption of filtered TC-B12 (7, 90).
Although both megalin and cubilin mediate endocytic uptake of vitamin B12, and both are heavily expressed in proximal tubule epithelial cells, a role for cubilin in kidney B12 uptake has not been established. Cubilin purified from kidney binds IF-bound B12, and uptake of IF-B12 in the kidney is inhibited by anti-cubilin antibodies (11). Minute amounts of IF can be detected in human serum and may be filtered, as IF has been identified in urine (111, 143). However, due to the very small amounts of B12 filtered in complex with IF, the significance of cubilin for renal uptake of B12 is dubious.
Folate.
A role of the FR in renal tubular folate uptake was hypothesized when FRs were identified in the kidney proximal tubule (66, 129) and further supported by kinetic studies showing that the urinary clearance of folate derivatives was inversely related to their affinity for the FR (127). The importance of the FR was established by the analysis of renal folate handling in mice with targeted gene knockout of folbp1 and folbp2 (10). Mice defective in folbp1 (equivalent to human FR) reveal a significant increase in renal folate clearance at both low-folate and normal-folate intakes, showing impaired tubular uptake of filtered folate (10). It was calculated that the amount of folate excreted in the urine of folbp1 null mice is 100 times higher than in wild-type mice, indicating that the tubular reabsorptive capacity related specifically to folbp1 in the low-folate situation is 4 nmol/24 h in mice. With an estimated 20,000 nephrons in the mouse, this corresponds to a transport rate of 0.15 fmolmin–1nephron–1. Folbp2 (equivalent to human FR)-deficient mice revealed lower serum folate levels compared with wild-type but no significant changes in urinary folate clearance (10). Thus, although mRNA corresponding to both the human equivalents of folbp1 and folbp2 has been demonstrated in the human kidney (116), the role of folbp2 in renal folate reabsorption remains unclear.
The rate of transtubular folate transport has been estimated using several other approaches. Perfusion of isolated rabbit proximal tubules revealed a reabsorptive capacity of 4.0 fmol·min–1·nephron–1, which should be compared with an estimated rabbit single-nephron filtration of folate 3 fmol/min (8). Micropuncture of single rat proximal tubules for 1 min with [3H]folic acid demonstrated tubular uptake at a rate of 0.65 fmol/mm tubule or 4.5 fmol/proximal tubule (128), close to the observed rate in isolated perfused rabbit tubules (8). In contrast, in vitro studies using cultured human proximal tubule cells suggested a specific apical-to-basolateral folate transport rate of only 0.12 fmol·min–1·cm–2 (89), considerably lower than that observed with perfused rabbit proximal tubules, indicating either lower activity of cells in vitro, possible effects of flow rate in microperfusion studies, or species differences, conceivably reflecting differences in serum folate levels. Studies using cultured human proximal tubule cells have suggested bidirectional transport (95), but tubular secretion of folate in vivo has not been established.
Uptake of folate by the FR is suggested to involve internalization of the FR-folate complex (129). Studies in monkey kidney MA104 cells and other cell lines indicated that binding is followed by invagination of the FR into caveolae rather than the clathrin-coated pit pathway (3). As the folate-FR complex clusters into caveolae, this is followed by acidification (76) and dissociation of the ligand (3). The FR is recycled to the plasma membrane by reopening of the caveolae. Later in vitro studies have challenged this hypothesis by showing that GPI-linked receptors concentrate in caveolae by cross-linking with antibodies, but not with folate (87, 106), that FRs can be endocytosed following stimulation (106), and that in KB cells derived from a carcinoma of the human nasopharynx most internalized FR bypasses caveolae (114). Experiments in CHO cells have suggested that FRs are internalized into a distinct GPI-anchored, protein-enriched compartment independent of clathrin (118). Thus FRs may be internalized by several different endocytic pathways depending on cell type and on the stimulus evoking internalization. Micropuncture of kidney proximal tubules showed endocytosis of folate-gold particles into coated pits and vesicles (8), and the FR has been localized to the compartments of the classic endocytic and recycling pathway (9, 14, 58). Also, caveolae are almost never observed in kidney proximal tubule cells (20), making it unclear whether this mechanism operates in these cells. Micropuncture with anti-FR antibodies (9), as well as kinetic studies (128), suggests rapid recycling of FRs to the plasma membrane for regeneration of folate-binding sites.
Several other mechanisms have been implicated in renal tubular folate transport, including dual-component transport systems (96) or even nonspecific pathways (97). Folate uptake has been studied in vitro using a number of different cell systems (4, 54, 67). In certain cell types, including KB cells and MA104 cells, folate uptake apparently depends on FRs. Other cell lines, i.e., mouse L1210 leukemia cells, utilize a high-capacity folate uptake system mediated by the reduced folate carrier (RFC). Thus folate uptake may be mediated by a receptor-mediated mechanism depending on the FR and/or carrier-mediated mechanisms, of which the RFC has been most extensively characterized (86). The RFC has been located to basolateral membranes in kidney tubules (146), suggesting that the RFC may be involved in basolateral folate uptake or in the cellular exit of reabsorbed folate. RFC represents a high-capacity, low-affinity transport system for folate with a Ki for 5-MTHF on the order of 2 µM. Targeted gene knockout of RFC is embryonically lethal; however, a limited number of mice can be rescued by folate supplementation of the dams. These mice revealed defects in erythro- and lymphopoiesis along with abnormalities in renal and seminiferous tubule development (157). Additional organic anion transporters, which may also transport folate, have been identified in the kidney (86). Thus a carrier-mediated mechanism may be responsible for the transport of folate out of endosomes, as well as for the exit of folate from the tubule cells.
In addition to the FR, megalin may also be involved in the tubular uptake of folate. SPR analysis, autoradiography, and uptake studies suggested that megalin mediates binding and internalization of soluble FBP (14). Folate bound to serum FBP is filtered as a complex. It may be estimated that <1% of filtered FBP is excreted (14), suggesting efficient tubular reabsorption by megalin-mediated endocytosis similar to other vitamin carrier proteins (27, 31). Approximately 108 nmol or 48 µg of FBP-bound folate may be recovered daily by megalin-mediated uptake, which could be important in individuals with low-folate intake. Thus FBP is involved in folate uptake both as a GPI-linked, membrane-associated receptor for filtered free folate and as a filtered, soluble, folate carrier protein binding to megalin.
A potential role for cubilin in the recovery of filtered folate is suggested by the important role of this receptor for the reabsorption of filtered albumin (6). Albumin binds to cubilin with an estimated Kd of 0.6 µm (6). Because albumin is a carrier of folate, along with other vitamins, cubilin may be involved in the uptake of folate, depending on the amount of filtered albumin. The significance of this remains to be established both in the normal kidney and under pathological conditions characterized by increased filtration of albumin.
Postendocytic Processing in the Kidney
Following internalization into renal proximal tubule cells, vitamins may be metabolized, stored, or released (Fig. 6). A recent study has shown endocytosis and lysosomal accumulation of a fluorescent folate probe using in vivo two-photon microscopy (121). Following intravenous injection of labeled folate into rats, there is a transient increase in the accumulation of label within the kidney at levels exceeding the liver; however, 24 h after injection, the amount of labeled folate within the kidney is significantly reduced by redistribution into other tissues (131), indicating that the kidney does not accumulate large amounts of folate. The endocytosed free folate is transported to the cytoplasm, possibly by a carrier protein (109). The reabsorbed folate may, in part, undergo metabolic transformation into other folate forms but is catabolized only to a very small extent (88, 96). Alternatively, folate may be transported across the tubular cells in a vesicular compartment, as suggested based on the finding of fluorescent-labeled folate in basolateral vesicles of the proximal tubule (121). However, no morphological evidence of such transport was observed following proximal tubule micropuncture with folate-gold particles (8) or radiolabeled folic acid (58).
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Alternatively, B12 may be transported along with TC across the tubular cell. Megalin-mediated transcellular transport of intact protein has been suggested for thyroglobulin (85) and for RBP (84). So far, this has not been confirmed in vivo, and the accumulation of free vitamin B12 along with rapid degradation of internalized TC in cultured proximal tubule cells strongly suggest that only the vitamin is transported through the cells. The mechanism, by which reabsorbed B12 is released from the tubular cells following reabsorption, is largely unknown. Both TC and HC, and possibly IF, are synthesized in proximal tubule cells in vitro (19, 104, 112). TC mRNA was identified in adult porcine and human kidney, whereas HC mRNA could not be identified in the adult porcine kidney (104). Whether B12 and carrier proteins are combined within in the cell before secretion or are secreted separately remains to be established.
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CONCLUSIONS AND FUTURE PERSPECTIVES |
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TOPABSTRACTFOLATEVITAMIN B12FOLATE, VITAMIN B12, AND...CONCLUSIONS AND FUTURE...GRANTSREFERENCES |
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The mechanism by which vitamins are further transported, processed, and released by the proximal tubule cells is largely unresolved (Fig. 6), although it may involve specific carriers associated with intracellular vesicular and basolateral membranes, as well as proximal tubule synthesis and secretion of carrier proteins. Further studies, including the use of inherited and genetically engineered models of defective vitamin transport as well as transfection studies with fluorescent-labeled carrier proteins, should provide clues to resolve these mechanisms and their possibly regulation. The cytoplasmic tail of megalin contains potential signaling motifs as well as domains interacting with cytosolic proteins (27, 42, 80, 94, 98, 158). Future studies may reveal signaling pathways, as has been implicated for other members of the LDLR family (56), possibly also involved in regulation of vitamin transport.
Most of the evidence establishing the mechanisms for renal tubular uptake of folate and B12 is based on experiments in animals, particularly in rodents. Studies in humans, including patients with renal disease and proteinuria as well as patients with inherited, specific receptor defects, should assess the importance of these mechanisms to vitamin homeostasis in humans.
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TOPABSTRACTFOLATEVITAMIN B12FOLATE, VITAMIN B12, AND...CONCLUSIONS AND FUTURE...GRANTSREFERENCES |
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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1 The present review will apply the term "folate" when referring to all different forms of the vitamin that may be converted into the active form. 
2 The term "vitamin B12" is chemically restricted to cyanocobalamin; however, the present review will refer to all potential biologically active cobalamins as vitamin B12 or B12. These include the coenzyme forms methylcobalamin and 5-deoxyadenosylcobalamin, as well as hydroxycobalamin and cyanocobalamin, all found in serum with methylcobalamin as the dominant form (45).
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TOPABSTRACTFOLATEVITAMIN B12FOLATE, VITAMIN B12, AND...CONCLUSIONS AND FUTURE...GRANTSREFERENCES |
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