Transport Of D-mannose Research Articles

Ontogeny of d-Mannose Transport and Metabolism in Rat Small Intestine

Oral mannose therapy is used to treat congenital disorders of glycosylation caused by a deficiency in phosphomannose isomerase. The segmental distribution and ontogenic regulation of D-mannose transport, phosphomannose isomerase, and phosphomannose mutase is investigated in the small intestine of fetuses, newborn, suckling, 1-month-old, and adult rats. The small intestine transports D-mannose by both Na(+)-dependent and Na(+)-independent transport mechanisms. The activities of both systems normalized to intestinal weight peak at birth and thereafter they decreased. In all the ages tested, the activity of the Na(+)-independent mechanism was higher than that of the Na(+)/mannose transport system. At birth, the Na(+)-independent D-mannose transport in the ileum was significantly higher than that in jejunum. Phosphomannose isomerase activity and mRNA levels increased at 1 month, and the values in the ileum were lower than in jejunum. Phosphomannose mutase activity in jejunum increased during the early stages of life, and it decreased at 1 month old, as does the amount of mannose incorporated into glycoproteins, whereas in the ileum, they were not affected by age. The phosphomannose isomerase/phosphomannose mutase activity ratio decreased at birth and during the suckling period, and increased at 1 month old. In conclusion, intestinal D-mannose transport activity and metabolism were affected by ontogeny and intestinal segment.

Metformin-stimulated Mannose Transport in Dermal Fibroblasts

The biguanide drug metformin stimulates AMP-activated protein kinase, a master regulator of cellular energy metabolism, and has antihyperglycemic activity due to attenuation of gluconeogenesis in hepatocytes and 2-fold stimulation of glucose transport by skeletal muscle. Here we identify a metformin-stimulated d-mannose transport (MSMT) activity in dermal fibroblasts. MSMT increased mannose uptake 1.8-fold and had greater affinity for mannose than basal mannose transport activity. It was attributed to robust stimulation of a transporter expressed weakly in untreated cells. MSMT was not explained by greater glucose transporter activity because metformin unexpectedly decreased transport of 2-deoxy-d-glucose and 3-O-methyl-d-glucose by fibroblasts. Effective inhibitors of MSMT retained specificity for the 3-, 4-, and 6-OH groups of the mannose ring but not the 2-OH group. Thus, MSMT could be strongly inhibited by glucose and 2-deoxy-d-glucose even though the latter was not a good transport substrate. MSMT was significant because in the presence of 2.5 microm mannose, metformin corrected experimentally induced deficiencies in the synthesis of glucose(3)mannose(9)GlcNAc(2)-P-P-dolichol and N-linked glycosylation. MSMT was also identified in congenital disorder of glycosylation types Ia and Ib fibroblasts, and metformin acted synergistically with 100 microm mannose to correct lipid-linked oligosaccharide synthesis and N-glycosylation in the Ia cells. In conclusion, metformin activates a novel fibroblast mannose-selective transport system. This suggests that AMP-activated protein kinase may be a regulator of mannose metabolism and implies a therapy for congenital disorders of glycosylation-Ia.

D-mannose transport and metabolism in isolated enterocytes.

D-mannose transport and metabolism has been studied in enterocytes isolated from chicken small intestine. In the presence of Na(+), the mannose taken up by the cells either remains free, is phosphorylated, is catabolized to H(2)O, or becomes part of membrane components. The mannose remaining free in the cytosol is released when the cells are transferred to an ice bath. The Na(+)-dependent D-mannose transport is electrogenic and inhibited by ouabain and dinitrophenol; its substrate specificity differs from SGLT-1 transporter. The Glut2 transporter inhibitors phloretin and cytochalasin B added following 30-min mannose uptake reduced the previously accumulated D-mannose, whereas these two agents increased the cell to external medium 3-O-methyl-glucose (3-OMG) concentration ratio. D-mannose efflux rate from preloaded D-[2-(3)H]-mannose enterocytes is Na(+)-independent. Phloretin did not affect D-mannose efflux rate, whereas it inhibited that of 3-OMG. Neither mannose uptake nor efflux rate were affected by fructose. It is concluded that part of the mannose taken up by the enterocytes is rapidly metabolized and that enterocytes have two D- mannose transport systems: one is concentrative and Na(+)-dependent and the other is Na(+)-independent and passive.

Rat kidney MAP17 induces cotransport of Na-mannose and Na-glucose in Xenopus laevis oocytes.

Renal reabsorption is the main mechanism that controls mannose homeostasis. This takes place through a specific Na-coupled uphill transport system, the molecular identity of which is unknown. We prepared and screened a size-selected rat kidney cortex cDNA library through the expression of mannose transport in Xenopus laevis oocytes. We have identified a membrane protein that induces high-affinity and specific Na-dependent transport of d-mannose and d-glucose in X. laevis oocytes, most likely through stimulation of the capacity of an endogenous transport system of the oocyte. Sequencing has revealed that the cDNA encodes the counterpart of the human membrane-associated protein MAP17, previously known by its overexpression in renal, colon, lung, and breast carcinomas. We show that MAP17 is a 12.2-kDa nonglycosylated membrane protein that locates to the brush-border plasma membrane and the Golgi apparatus of transfected cells and that it is expressed in the proximal tubules of the kidney cortex and in the spermatids of the seminiferous tubules. It spans twice the cell membrane, with both termini inside the cell, and seems to form homodimers through intracellular Cys55, a residue also involved in transport expression. MAP17 is responsible for mannose transport expression in oocytes by rat kidney cortex mRNA. The induced transport has the functional characteristics of a Na-glucose cotransporter (SGLT), because d-glucose and alpha-methyl-d-glucopyranoside are also accepted substrates that are inhibited by phloridzin. The corresponding transporter from the proximal tubule remains to be identified, but it is different from the known mammalian SGLT-1, -2, and -3.

Na +-dependent d-mannose transport at the apical membrane of rat small intestine and kidney cortex

The presence of a Na +/ d-mannose cotransport activity in brush-border membrane vesicles (BBMV), isolated from either rat small intestine or rat kidney cortex, is examined. In the presence of an electrochemical Na + gradient, but not in its absence, d-mannose was transiently accumulated by the BBMV. d-Mannose uptake into the BBMV was energized by both the electrical membrane potential and the Na + chemical gradient. d-Mannose transport vs. external d-mannose concentration can be described by an equation that represents a superposition of a saturable component and another component that cannot be saturated up to 50 μM d-mannose. d-Mannose uptake was inhibited by d-mannose≫ d-glucose>phlorizin, whereas for α-methyl glucopyranoside the order was d-glucose=phlorizin≫ d-mannose. The initial rate of d-mannose uptake increased as the extravesicular Na + concentration increased, with a Hill coefficient of 1, suggesting that the Na +: d-mannose cotransport stoichiometry is 1:1. It is concluded that both rat intestinal and renal apical membrane have a concentrative, saturable, electrogenic and Na +-dependent d-mannose transport mechanism, which is different from SGLT1.

A Na+-dependent D-mannose transporter in the apical membrane of chicken small intestine epithelial cells

The presence of a Na+/D-mannose cotransporter in brush-border membrane vesicles (BBMV) isolated from chicken small intestine was examined. In the presence of an electrochemical gradient for Na+, but not in its absence, D-mannose was accumulated transiently by the BBMV. D-Mannose uptake into the BBMV was energized by both the membrane potential and the chemical gradient for Na+. The relationship between D-mannose transport and external D-mannose concentration was described by an equation that represented the superposition of a saturable component (Michaelis-Menten constant Km 12.5 microM) and another component unsaturatable up to 80 microM D-mannose. D-Mannose uptake was inhibited by various substances in the following order of potency: D-mannose>>D-glucose>phlorizin>phloretin>D-fructose. For the uptake of alpha-methyl-glucopyranoside the order was D-glucose=phlorizin>>phloretin=D-fructose=D-mannose. The initial rate of D-mannose uptake increased as the extravesicular [Na+] increased, with a Hill coefficient of 1, suggesting that the Na+:D-mannose cotransport stoichiometry is 1:1. It is concluded that the intestinal apical membrane has a saturable, electrogenic and concentration- and Na+-dependent mannose transport mechanism that differs from the sodium-dependent glucose transporter SGLT1.

Expression and molecular characterization of rat renal D-mannose transport in Xenopus oocytes.

Renal reabsorption appears to play a major role in d-mannose homeostasis. Here we show that in rat kidney, the transport of d-mannose by brush border membrane vesicles from tubular epithelial cells involves an uphill and rheogenic Na-dependent system, which is fully inhibited by d-mannose itself, incompletely inhibited by d-glucose, d-fructose, phloridzin, and phloretin, and noninhibited by l-mannose or disaccharides. In addition, this system exhibits both low capacity (112.9+/-15.6 pmol/mg/second) and high affinity (0.18+/-0.04 mm), with a 2:1 stoichiometry for the Na:d-mannose interaction, and low affinity for sodium (16.6+/-3.67 mm). We also show expression of d-mannose transport by Xenopus laevis oocytes injected with rat renal polyA(+) RNA. Kinetic analysis of the expressed transport was performed after RNA enrichment by fractionation through a sucrose density gradient and was shown to be identical to that measured in membrane vesicles. The RNA species encoding the expressed transport has a small mean size, 1 kb approximately, and shows no homology with the SGLT family of Na-dependent d-glucose transporters, as shown by low stringent RT-PCR and northern analysis. The expressed transport is specific for d-mannose, since in spite of a significant inhibition by d-glucose and d-fructose, neither of these two substrates was transported above the level of the water-injected oocytes.

Rapid uptake and phosphorylation of D-mannose, and limited D-mannose 6-phosphate isomerization in the glycolytic pathway of bloodstream forms of Trypanosoma brucei gambiense.

Bloodstream forms of the parasitic protozoa Trypanosoma brucei gambiense derive all of needed energy through an unusual glycolysis. In an earlier study, we showed that D-mannose specifically inhibited the growth of bloodstream forms of T. b. gambiense. We investigated D-mannose transport into the T. b. gambiense bloodstream forms and its metabolism in the initial phase of the glycolytic pathway. D-Mannose was transported rapidly into the bloodstream forms of T. b. gambiense (K(m) = 378 microM), and D-glucose competitively inhibited D-mannose uptake. D-Mannose and D-glucose are transported into bloodstream trypanosomes by the same carrier. Hexokinase from the bloodstream trypanosomes could convert D-mannose to D-mannose 6-phosphate (K(m) = 155.8 microM; Vmax = 0.93 mumol/min/mg protein); with kinetic properties very similar to D-glucose phosphorylation (K(m) = 199.4 microM; Vmax = 1.15 mumol/min/mg protein). D-Mannose 6-phosphate could be further metabolized in the glycolytic pathway. However, the metabolic rate was extremely slow, and D-mannose 6-phosphate accumulated in the glycosomes. D-Mannose may cause growth inhibition of bloodstream trypanosomes through an extremely high concentration of D-mannose 6-phosphate in the glycosomes.

A D-mannose transport system in renal brush-border membranes.

Dog renal brush-border membrane vesicles (BBMV) from whole kidney cortex contain both low-affinity, high-capacity and high-affinity, low-capacity Na-dependent D-glucose cotransporters. D-Mannose is an epimer of D-glucose, differing in structure only in the axial, rather than equatorial, orientation of the hydroxyl group at the C-2 position of the pyranose ring. Uptake experiments of radioactive sugars into BBMV by standard Millipore filtration were performed to determine whether D-mannose shares either, or both, of the D-glucose carriers or if it is transported by an independent system. Transport of D-mannose occurs into an osmotically active space and is saturable and sodium dependent with a 1:1 Na:D-mannose stoichiometry, Km of 0.063 mM, Vmax of 3.6 nmol.mg-1.min-1, 25 degrees C, and pH 7.4. When an NaSCN electrochemical gradient was present, an "overshoot" was present, indicating active cotransport. Up to 50 mM D-mannose did not inhibit sodium-dependent D-glucose or alpha-methylglucoside uptake (0.01-20 mM). Sodium-dependent D-mannose uptake was inhibited by the following compounds in order of decreasing effectiveness: fructose greater than mannoheptulose greater than 2-deoxy-D-glucose greater than 2-fluoro-2-deoxy-D-glucose much greater than phloretin, cytochalasin B, galactose, 3-O-methyl-D-glucose, and L-mannose. Phlorizin also inhibited D-mannose uptake, but the high concentration required and the fact that a competitive pattern of inhibition could not be demonstrated contrasted with its effect on D-glucose transport.(ABSTRACT TRUNCATED AT 250 WORDS)

Renal sugar transport in the winter flounder. VI. Reabsorption of D-mannose

The transport of D-mannose (Man) in flounder kidney was studied using renal clearance techniques in vivo and brush border membrane (BBM) vesicles in vitro. At plasma concentrations of 50-100 microM Man, the winter flounder (Pseudopleuronectes americanus) reabsorbed up to 70% of the filtered sugar. Man phosphates, but not free Man, accumulated in renal cells. Reabsorption of Man was reduced by phlorizin, D-glucose, methyl-alpha-D-glucoside, methyl-alpha-D-mannoside, and 2-deoxy-D-glucose. In BBM vesicles a Na+-dependent, phlorizin-sensitive overshoot in Man uptake (10 microM) was seen. Na+-dependent Man uptake was saturable, with an apparent Km of 127 microM. The transport properties for Man were identical in BBM vesicles from the winter flounder and southern flounder (Paralichthys lethostigma). The transport specificity was determined by cis-inhibition and trans-stimulation experiments with BBM. Glucose, galactose, 1,5-anhydro-D-mannitol (i.e., 1-deoxymannose), 2-deoxy-2-fluoro-D-glucose, and methyl-alpha-mannoside were shown to share the carrier-mediating mannose transport. 2-Deoxyglucose, methyl-alpha-2-deoxy-D-glucoside, and both the isomers (alpha and beta) of methyl-D-glucoside did not. In contrast, alpha-methyl-D-glucoside inhibited D-glucose transport both in vivo and in BBM vesicles. It is concluded that Man reabsorption in the flounder occurs via a Na+-cotransport system that also handles glucose but that differs from the glucose/methyl-alpha-D-glucoside reabsorptive pathway in that 1) an oxygen on C-1 is not required, and 2) an axial configuration for -OH on C-2 (C1 conformation) is readily accommodated.

Evidence for a specific transport of D-hexoses across the human term placenta in vitro

Isolated cotylidons of human term placentas are perfused artificially on the fetal and maternal side. The relative transfer rates of radioactive labelled D-glucose, L-glucose, D-mannose and D-mannitol across the placenta are measured and the inhibition of these transports by phloretin is studied: 1. Transfer rates of D-glucose and D-mannose exceed that of L-glucose about 1.5-4 times. 2. Phloretin (10(-3) mol/l) decreases the transports of D-hexoses, whereas the transport of L-GLUCOSE REMAINS UNAFFECTED. 3. If the concentration of D-glucose is increased, the transport of D-mannose is inhibited competitively. 4. L-glucose and D-mannitol equal in transfer rates. These results show, that D-hexoses cross the human placenta by a specific carrier and by simple diffusion.

The structural requirement for C 1OH for the active transport of d-mannose and 2-deoxy- d-hexoses by renal tubular cells

The transport of methyl-α-glycopyranosides of d-mannose, 2-deoxy- d-glucose and 2-deoxy- d-galactose, as well as of 1,5-anhydro-2-deoxy- d-glucitol in slices of rabbit kidney cortex was investigated. 1. 1. In contrast to the respective actively transported hexoses, their methyl-glycopyranosides (0.1–1 mM) were not accumulated in the cells against marked concentration gradients. The entry of the glycosides into the cells was not significantly affected by 0.5 mM ouabain or absence of Na +, and was only slightly inhibited by 0.5 mM phlorizin. 2. 2. The glycopyranosides (5 mM) did not inhibit the active transport of the respective hexoses (1 mM). 3. 3. 1,5-Anhydro-2-deoxy- d-glucitol (0.1–1 mM) was not accumulated in the cells against its concentration gradient, and its entry was not affected by 2-deoxy- d-glucose. Conversely, the active transport of 2-deoxy- d-glucose (1 mM) was not significantly inhibited by a 5-fold molar excess of its 1-deoxy-derivative. 4. 4. It is concluded that, as opposed to the structural requirements for the transport of d-glucose and d-galactose, C 1OH is essential for the interaction with the carrier(s) mediating the active transport of d-mannose, 2-deoxy- d-glucose and 2-deoxy- d-galactose.

Specificity of monosaccharide transport in dog kidney.

Specificity of monosaccharide transport in dog kidney.

Intestinal sugar transport: Ionic activation and chemical specificity

The mode of absorption of several monosaccharides was studied in vitro with segments and everted sacs of hamster small intestine. 1. 1. Na + reduced the apparent K m of transport of the actively transported d-galactose, 3-methyl- d-glucose, α-methyl- d-glucoside, d-xylose and l-glucose. The ‘nontransported’ d-arabinose, l-arabinose, l-rhamnose, l-mannose and l-fucose showed Michaelis-Menten kinetics, but their K m 's were not significantly altered by Na +. The ν max of all the sugars tested was identical and independent of Na +. Inhibition of entry of nontransported sugars by d-galactose and by phlorizin was demonstrated. 2. 2. By the criteria of Na + dependence, inhibition by phlorizin and ouabain and inhibition by transported sugars, d-mannose and d-fructose were also shown to interact with the joint sugar carrier. The transport of d-mannose appears to be active, but rapid metabolism of the two sugars precluded a quantitative determination of transport parameters. 3. 3. The data suggest a dual specificity of a joint sugar carrier: In the absence of Na + its affinity for many diverse sugars is low; the presence of Na + increases the affinity for only some of these sugars. The potential for active transport depends on the extent of this activation by Na + and varies with different sugars from negligible to very great. 4. 4. With low concentrations of sugar the asymmetry of transport increases towards a limiting value which depends on the ratio K m( Na + free) K m( Na +) . Active transport occurs with sugars where this ratio >3−5, provided their concentration is below a critical value which also parallels the K m ratio.

Active transport of D-mannose in the small intestine

A low capacity active transport system for D-mannose is uncovered in the isolated small intestine of the frog. The active transport is sodium dependent and is inhibited by 10 −5M ouabain.