Folate is an essential micronutrient, the primary function of which is as a carrier of single-carbon units for the biosynthesis of thymidylate, purines, methionine and glycine(Reference Wani, Hamid and Kaur1, Reference Zhao, Matherly and Goldman2). Maintenance of intracellular folate homeostasis is vitally important; particularly for rapidly replicating cells such as colonic epithelial cells. Indeed, perturbed 1-carbon transfer reactions resulting from folate depletion and disrupted folate metabolism predispose normal colonic epithelial cells to neoplastic transformation through aberrant DNA synthesis, integrity, repair and methylation(Reference Choi and Mason3–Reference Kim5). A number of epidemiological and clinical studies linking decreased folate status with risk of colorectal cancer support this. Folate is absorbed in the proximal small intestine after the polyglutamate chain is hydrolysed by glutamate carboxypeptidase II. The hydrolytic step is followed by membrane transport of monoglutamyl folate into cells by folate transporters(Reference Qiu, Jansen and Sakaris6–Reference Nguyen, Dyer and Dunning8). Whereas monoglutamates are the only circulating forms of folate in blood and the only forms of folate that are transported across the cell membrane, once taken up into cells, cellular folate exists primarily as polyglutamates(Reference Hamid, Wani and Kaur9). Intracellular folate is converted to polyglutamates by folylpolyglumate synthase(Reference Wani, Hamid and Kaur1). The polyglutamylation of cellular folates is a form of metabolic trapping, allowing the retention of folate that would otherwise be lost to efflux from cells(Reference Egan, Sirlin and Rumberger10). In the colon, folate – exogenous as well as synthesised by normal microflora – undergoes the initial step of transport across the brush border membrane (BBM) and then the exit of folate across basolateral membrane (BLM) into portal circulation. The mechanism of absorption of dietary folate in the BBM and BLM of colon has been investigated and the existence of pH-dependent, 4,4′-diisothicyano-2,2′-stilbenedisulfonic acid (DIDS)-sensitive, carrier-mediated uptake system has been demonstrated with the involvement of reduced folate carrier (RFC) in the exit of folate out of colonocytes(Reference Wani and Kaur7, Reference Dudeja, Kode and Alnounou11). However, the role of proton-coupled folate transporter (PCFT) still remains silent.
Deficiency of folate is highly prevalent throughout the world and alcohol ingestion has been the major contributor(Reference Sakuta and Suzuki12, Reference Hamid and Kaur13). Approximately 60–70 % of binge drinkers are folate deficient(Reference Bode and Bode14). Regardless of the cause, folate deficiency leads to a variety of clinical abnormalities like megaloblastic anaemia, growth retardation etc., whereas optimisation of folate homeostasis prevents certain disorders like neural tube defects(Reference De Marco, Calevo and Moroni15). Earlier, we have reported the derangement of PCFT and RFC across colon apical membrane (CAM) and of RFC on intestinal membrane surfaces during chronic alcohol ingestion in rats(Reference Wani and Kaur7, Reference Hamid and Kaur13, Reference Hamid, Kaur and Mahmood16–Reference Hamid, Wani and Rana18). However, no studies have been attempted so far to delineate the distribution of folate transporters to lipid microdomains and activity of folate transport system in BLM under conditions of folate malabsorption. For this, the present work was sought to characterise the folate transport across the colon BLM and the role of the folate transporters therein during alcoholism. We used rats as an experimental model of chronic alcoholism based on the published studies demonstrating their resemblance and utility as a model in order to relate to humans on the basis of blood and intestinal alcohol concentration as well as plasma folate levels(Reference Hamid, Wani and Rana18–Reference McMartin and Collins20). Such mechanistic insights could lead to strategies for deducing folate transport regulation in diverse cellular microenvironments and will be important for designing therapeutic targets involving derangements in folate transport systems in primary absorptive epithelia.
Materials and methods
Radiolabelled 5-[14C]-methyltetrahydrofolate, potassium salt with specific activity 24·0 Ci/mmol (88·8 × 1010 Bq/mmol) were purchased from Amersham Pharmacia Biotech (Hong Kong). Color brust™ electrophoresis marker (molecular weight 8000–220 000) was purchased from Sigma Chemical Company (St Louis, MO, USA). Total RNA Extraction Kit was purchased from Taurus Scientific (Cincinnati, OH, USA). Moloney Murine Leukemia Virus RT (RevertAid™ M-MuLV RT) kit was purchased from the MBI Fermentas, Life Sciences (Glen Burnie, MD, USA). RNA later (RNA stabilisation solution) was obtained from Ambion, Inc. (Austin, TX, USA). Primary antibodies rabbit anti-rat reduced folate carrier (rRFC) and anti-rat proton-coupled folate transporter (rPCFT) polyclonal antibodies were raised in rabbits in our laboratory(Reference Wani and Kaur7). Horseradish peroxidase labelled goat anti-rabbit-IgG secondary antibodies were purchased from G Biosciences (St Louis, MO, USA). Enhanced Chemiluminescence Detection Kit was purchased from Biological industries Limited (Kibbutz Beit Haemek, Israel). Metal enhanced 3,3′-diaminobenzidine substrate kit was purchased from Thermo Fisher Scientific, Inc. (Rockford, IL, USA). Cryoprotected Lactobacillus casei bacterial strain (MTCC 1423) was purchased from IMTECH (Chandigarh, India).
Young adult male albino rats (Wistar strain) weighing 100–150 g (2–3 months old) were obtained from the Institute's Central Animal House. The animals were housed in clean wire mesh cages with controlled temperature (23 ± 1°C) and humidity (45–55 %) and had a 12 h dark–12 h light cycle throughout the study. The rats were randomised into two groups of twelve animals each. The rats in group I were given 1 g ethanol (20 % solution)/kg body weight per d and those in group II received isoenergetic amount of sucrose (36 % solution) orally by Ryle's tube daily for 3 months. The rats were fed ad libitum commercially available pellet diet (Ashirwad Industries, Ropar, India) and water. Animals from both the groups were killed under anaesthesia using sodium pentothal.
The protocol of the study was approved by ‘Institutional Animal Ethical Committee’ and ‘Institutional Biosafety Committee’.
Preparation of colon basolateral membrane vesicles
Basolateral membrane vesicles (BLMV) from colon was prepared by the self-generating percoll gradient method(Reference Scalera, Storelli and Storelli-Joss21) as described earlier(Reference Hamid, Kiran and Rana22). The mucosa was scraped from the proximal colon. The scrapings were homogenised in ice-cold buffer containing 250 mm-mannitol and 12 mm-HEPES–Tris, pH 7·4 using a Waring blender for 3 min and then centrifuged at 2500 g for 20 min. The supernatant was then centrifuged at 22 000 g for 25 min and the resulting fluffy layer of the pellet resuspended in the same buffer followed by homogenisation in glass Teflon homogeniser. The resulting homogenate was mixed with percoll at a concentration of 15·4 % and centrifuged at 48 000 g for 2 h. A distinct band of BLMV was seen at the upper one-third of the percoll gradient. The band was aspirated by a syringe and suspended in buffer composing 100 mm-mannitol, 100 mm-KCl, 12 mm-HEPES–Tris, pH 7·4 and centrifuged at 48 000 g for 20 min. The pellet obtained was resuspended in loading buffer containing 280 mm-mannitol and 20 mm-HEPES–Tris, pH 7·4 and centrifuged at 48 000 g for 20 min twice in order to wash out the residual percoll from membrane preparation. The final pellet representing purified BLMV was suspended in loading buffer (280 mm-mannitol, 20 mm-HEPES–Tris, pH 7·4) at 5 mg/ml protein concentration. Purity of the membrane preparations was checked by measuring the specific activities of Na+, K+-ATPase in BLMV and in original homogenate.
Transport of 5-[14C]-methyltetrahydrofolate
Uptake studies were performed at 37°C using the incubation buffer (100 mm-NaCl, 80 mm-mannitol, 10 mm-HEPES, 10 mm-3-(N-morpholino)ethanesulfonic acid (MES), pH 7·0). A quantity of 10 μl of vesicles (50 μg protein) was added to the incubation buffer containing 5-[14C]-methyltetrahydrofolate at a concentration as specified. The initial rate of transport was determined by stopping the reaction after 20 s by adding ice-cold stop solution containing 280 mm-mannitol, 20 mm-HEPES–Tris, pH 7·0 followed by rapid vacuum filtration(Reference Hamid, Wani and Rana18, Reference Dev, Ahmad Wani and Kaur23).
Total RNA was isolated from the colon by using total RNA extraction kit and complementary DNA synthesis was carried out from the purified and intact total RNA according to the manufacturer's instructions. Expression of RFC, PCFT and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was evaluated using sequence-specific primers corresponding to the sequence in the open reading frame. PCR mixture (20 μl) was prepared in 1 × PCR buffer consisting of 0·6 U of Taq polymerase, 2 μm of each primer for rGAPDH, rPCFT and rRFC along with 200 μm of each deoxyribonucleotide triphosphate. In optimised PCR, the initial denaturation step was carried out for 2 min at 95°C. The denaturation, annealing and elongation steps were carried out, respectively, for 1 min at 94°C, 45 s at 64°C (PCFT) or 56°C (GAPDH) and 1 min at 72°C for thirty-five cycles. In the case of RFC denaturation, annealing and elongation steps were carried out, respectively, for 30 s at 94°C, 30 s at 52·1°C, 30 s at 72°C for thirty-five cycles. The final extension step was carried out for 10 min at 72°C. The primers were designed using Primer3 Input (version 0.4.0; http://primer3.sourceforge.net). The sequences of the primers used were as follows: 5′-CATGCTAAGCGAACTGGTGA-3′ (sense) and 5′-TTTCCACAGGACATGGACA-3′ (antisense) for RFC, AAGCCAGTTATGGGCAACAC (sense) and GGATAGGCTGTGGTCAAGGA (antisense) for PCFT. The expected PCR products of size 120, 300 and 400 bp were obtained for rRFC, rPCFT and rGAPDH, respectively when electrophoresed on 1·2 % agarose gel. The densitometric analyses of products were determined by using ‘Scion image’ software (Scion Image, Frederick, MD, USA).
Western blot analysis
For protein expression studies, colon BLMV (100 μg) were resolved on 10 % SDS-PAGE and transferred to polyvinylidene fluoride membrane for 20 min at 15 V. Western blotting was performed using the procedure described by Towbin et al. (Reference Towbin, Staehelin and Gordon24) using polyclonal primary antibodies as rabbit anti-rat RFC (1:800 dilutions) raised against the specific region of rat RFC synthetic peptide corresponding to amino acids 494–512(Reference Said, Chatterjee and Haq25). The polyclonal antibodies against PCFT (1:1000 dilutions) were raised against the specific region of rat PCFT synthetic peptide corresponding to amino acids 442–459. Secondary antibodies used were goat anti-rabbit IgG-horseradish peroxidase-labelled (1:20 000 dilutions). The bands were visualised by either metal enhanced 3,3′-diaminodbenzidine substrate kit or enhanced chemiluminescence detection kit according to the manufacturer's instructions. The quantification of the blots was carried out by using ‘Scion image’.
Floatation on a discontinuous Optiprep density gradient
Lipid rafts (LR) were isolated by floatation on Optiprep density gradient(Reference Hanwell, Ishikawa and Saleki26) as described earlier(Reference Wani and Kaur7). Briefly, membrane preparations were centrifuged at 100 000 g for 30 min at 4°C and then resuspended and incubated for 30 min at 4°C in TNE buffer containing 25 mm-Tris (pH 7·4), 150 mm-NaCl, 5 mm-EDTA and 1 % Triton X-100 supplemented with 1 × complete protease inhibitor cocktail. The membranes were then adjusted to 40 % final concentration of Optiprep and layered at the bottom of density gradient with steps of final concentrations of 35, 30, 25 and 20 % of Optiprep in TNE buffer. TNE buffer was laid on the top of the gradient, which was then centrifuged at 215 000 g for 4 h at 4°C. Fractions were collected from the top of the gradient and then analysed by Western blotting. Proteins in the top four fractions are considered to be raft-associated(Reference Oliferenko, Paiha and Harder27). Protein concentrations in each fraction were assessed by using better Bradford kit (Bio Basic Inc., East Markham, ON, Canada).
Freshly removed colon was cut followed by fixing in sufficient amount of 10 % formalin(Reference Zhang, Shao and Xie28). Paraffin sections of 4 μm thickness on poly-l-lysine-coated slides were baked overnight at 37°C. Endogenous peroxidase was quenched by pretreatment with 1 % H2O2 in methanol for 20 min followed by washings in PBS. Slides were put in primary diluted antibody (rabbit polyclonal anti-rat RFC and PCFT (1:200) for 2 h at 37°C followed by secondary antibodies as goat anti-rabbit IgG-horseradish peroxidase (1:200)). Presence of antibody at specific site(s) was revealed using freshly prepared 3,3′-diaminobenzene(Reference Sobierajska, Glos and Daborowska29) and H2O2 at room temperature for 3–5 min and counter-staining with haematoxylin.
Estimation of folate by microbiological assay
The folate estimations were determined by microtitre plate assay using L. casei as described earlier(Reference Hamid, Wani and Rana18). For intracellular folate concentrations in colon, a 10 % homogenate of colon was made in phosphate buffer of pH 6·3 containing 5 mg/ml ascorbate. The homogenate was incubated at 110°C for 10 min followed by centrifugation at 300 rpm for 10 min. Then, 0·1 ml of the supernatant was treated with 0·02 ml of rat plasma conjugase in 0·375 ml of phosphate buffer of pH 4·5. The free folate was then determined by a standard microbiological microtitre plate assay using L. casei. All the steps were carried out in aseptic conditions.
The data were computed as means and standard deviations. Group means were compared by using the Student's t test and ANOVA was used wherever necessary. The acceptable level of significance was less than 5 % for each analysis. The power of the study was 0·80.
Folate levels in colon
As the present study dealt with folate malabsorption during alcoholism, the determination of folate levels was of prime importance. The results showed that a significant reduction (P < 0·01) in colonic tissue folate levels (the levels were 8·8 (sd 0·09) and 4·2 (sd 0·05) nmol/g tissue for control and ethanol fed, respectively) in chronic alcoholism, confirming the association of alcoholism with folate deficiency.
Kinetic characterisation of folate transport across colon basolateral membrane
Folate uptake was studied at different time intervals from 10 to 240 s, the uptake attained maximum value at 120 s in control and 240 s in ethanol-fed rats (Fig. 1(a)), with 14–23 % (P < 0·05, < 0·001) less folate uptake at different time intervals in ethanol-fed group as compared to control. Further, kinetic constants were determined in BLMV as a function of 5-[14C]-methyltetrahydrofolate concentration varying from 0·125 to 8·0 μm for 20 s (Fig. 2(a)). There was a gradual increase in folate uptake in the two groups of rats with increase in substrate concentration. In the ethanol-fed group, there was a significant reduction of 15–50 % in uptake as compared to the control group at different concentrations of folate used. The data were then extrapolated as a Lineweaver–Burk plot and kinetic constants were determined (Fig. 2(b)). The K m value in the ethanol-fed group was found to be 5·0 (sd 0·56) μm in comparison to 2·8 (sd 0·81) μm of control group (P < 0·01). In addition, V max in control and ethanol-fed groups were 76·33 (sd 5·4) and 43·66 (sd 4·95) pmol/30 s per mg protein (P < 0·001), respectively.
To determine whether a proton gradient-dependent exchange process is involved in folate transport across the colon BLM, the effect of transmembrane pH was studied (Fig. 1(b)) keeping inside pH constant at 7·4. As the pH was increased in the extra-vesicular medium from 5·0 to 8·0, the uptake was constant till 6, and started increasing beyond that, with maximum uptake at pH 7·0 in both the groups (Fig. 1(b)). In addition, a significant reduction of the order of 33–40 % (P < 0·01, < 0·01, < 0·001) in transport was observed in the ethanol-fed group at and above pH 7·0; however, no such uniform reduction was observed in the acidic pH range.
Further, in order to determine the specificity of the folate transporters (Fig. 2(c)), the folate transport was measured in the presence of the structural analogues methotrexate and unlabelled folic acid and inhibitors; thiamine pyrophosphate, reported to be a substrate of RFC(Reference Zhao, Gao and Wang30) and hemin, is a weak inhibitor of folate transport via heme carrier protein 1(Reference Qiu, Jansen and Sakaris6). The structural analogues methotrexate and folic acid decreased the uptake by 41 (P < 0·001) and 44 % (P < 0·01) in control, and 41 (P < 0·01) and 33 % (P < 0·05) in ethanol-fed rats, respectively, confirming the specificity of folate transporters. The inhibitor thiamine pyrophosphate significantly decreased the uptake by 20 (P < 0·05) and 38 % (P < 0·001) in control and ethanol-fed rats, respectively, while hemin did not change the uptake significantly.
To study the role of S–S groups (Fig. 2(d)), the effect of addition of dithiothreitol or Cleland's reagent on the transport of folate revealed decreased transport of folate by 56 % (P < 0·01) in control and 32 % in ethanol-fed rats (P < 0·01; Fig. 2(d)). The determination of the influence of ATP on folate uptake showed that there was not any significant change in the uptake of folate across BLM in both the groups (Fig. 2(d)).
Expression of the proton-coupled folate transporter and reduced folate carrier in colon; association with lipid rafts
In order to elucidate the mechanism of reduced folate transport in chronic alcoholism, transcriptional and translation regulations of the RFC and PCFT were studied. The relative mRNA for the PCFT was approximately 1·8 fold (44 %) lower (P < 0·01) while that for the RFC was approximately 1·3 fold (23 %) lower (P < 0·01) in the ethanol-fed group (Fig. 3(a) and (b)).
Further, to investigate the effect of chronic alcohol feeding on the level of expression of the PCFT and the RFC protein, we performed Western blotting on the colon BLM protein of both the groups of rats (Fig. 3(c) and (d)). The results showed a significant decrease of 1·3 fold (24 %) in the level of expression of the PCFT (P < 0·05) and 2·3 fold (57 %) in the levels of RFC (P < 0·01) proteins in ethanol-fed rats (Fig. 3).
LR are the specialised microdomains of the plasma membrane that are essential for the normal functioning of various membrane transporters(Reference Anderson and Jacobson31–Reference Annaba, Sarwar and Kumar33). We sought to determine whether the folate transporters (PCFT and RFC) are associated with lipid microdomains of the colon basolateral membrane of rat. We had validated this technique earlier by measuring the specific activity of alkaline phosphatase (well-known marker for LR) in all the fractions collected from gradient using CAM(Reference Wani and Kaur7). The pattern of specific activity of alkaline phosphatase in all these fractions had revealed a gradient with considerable activity in the top floating fractions(Reference Wani, Hamid and Kaur1–Reference Kim4), indicating that these fractions contained LR. So the top fractions isolated from the gradient using colon BLM were subjected to Western blotting for the PCFT and the RFC (Fig. 3(e) and (h)). We found the presence of the PCFT and RFC protein in the floating fractions on the top five fractions (20–30 %) with negligible or no expression thereafter of Optiprep density gradient. Together, these data provide strong evidence that the majority of the PCFT and the RFC pool are associated with the lipid raft microdomains. Moreover, chronic alcoholism leads to a decreased association of both the PCFT and the RFC to the LR (Fig. 3(e) and (h)). The extent of decrease was 1·23- to 1·41-fold for PCFT (P < 0·01 and < 0·05) and 1·12- to 1·21-fold for RFC (P < 0·01, < 0·05), respectively, which is in accordance with the decreased levels of these transporters in the colon BLM.
Localisation of proton-coupled folate transporter and reduced folate carrier in colon
As there was a significant decrease in RFC and PCFT expression across colon BLM, we studied the localisation of these transporters in colon by immunohistochemistry (Fig. 4). The localisation of the RFC and PCFT was seen at both the apical and basolateral side membranes of colon. In ethanol-fed rats, there was marked reduction in the intensity of RFC and PCFT positive cells in colon (Fig. 4).
The observed reduced folate levels in the colon of ethanol-fed rats suggested the association of chronic alcoholism with colonic folate malabsorption. After the transport of folate across the CAM, the folate is transported across colon BLM to portal circulation. The higher values of K m (5·0 (sd 0·56) μm in comparison to 2·8 (sd 0·81) μm of the control group (P < 0·01) and decreased V max in ethanol-fed rats suggested that the folate exit across the BLM occurs less efficiently in chronic alcoholism and thus can reflect its lower availability in portal circulation. Also, a higher value of K m, i.e. 2·8 (sd 0·81) μm of colon BLM v. 1·42 (sd 0·13) μm of intestinal BLM, and 1·5 (sd 0·19) of the CAM(Reference Wani and Kaur7, Reference Hamid, Kiran and Rana22) suggested that the transport of folate across colon BLM occurs less efficiently as compared to intestinal BLM and CAM.
In order to determine the chemical driving force for the uphill folate transport, the neutral/alkaline pH was found to be the energising force in the BLM. The results depicted that neither the inwardly nor the outwardly directed H+ gradient is responsible for the folate uptake, as maximum folate uptake was observed at pH 7·4 inside and 7·0–7·4 outside pH, supporting the earlier observations, which suggests that folate transport across colon basolateral membrane occurs at neutral pH(Reference Dudeja, Kode and Alnounou11) and displayed similar characteristics as of intestinal BLM(Reference Hamid, Kiran and Rana22). Moreover, for the evaluation of the specificity of the folate transport system, structural analogues significantly inhibited the folate uptake. Less decrease in the folate transport in the presence of structural analogues methotrexate and unlabelled folic acid might be due to less affinity of the folate transporters to these substrates as compared to 5-methyltetrahydrofolate. The presence of thiamine pyrophosphate significantly reduced the folate transport across the BLM while the hemin did not change the uptake significantly. This suggested that the RFC was the main transporter involved in the folate exit across colon basolateral membrane, supporting the earlier contention which suggests that folate uptake via RFC is tissue specific(Reference Kumar, Nguyen and Gonzales34) and PCFT shows maximum transport activity at acidic pH(Reference Qiu, Jansen and Sakaris6, Reference Inoue, Nakai and Ueda35). This again supports the earlier results which showed maximum uptake at alkaline neutral pH, which is characteristic of folate uptake by RFC, confirming the results that neutral pH is the characteristic of folate uptake across the colon BLM, as RFC transport folate in neutral pH(Reference Qiu, Jansen and Sakaris6, Reference Inoue, Nakai and Ueda35, Reference Zhao, Qiu and Tsai36). Moreover, the folate uptake in BLM was sensitive to S–S group, suggesting that S–S bond(s) in its intact form is (are) required for the transport activity of folate transporters and the transport was found to be energy-independent and the transport was not mediated by ATP-binding cassette transporters, as there was no significant change in activity of folate transport in the presence of ATP.
The decreased V max of folate uptake process observed in ethanol-fed rats could relate to the reduced number of PCFT and RFC molecules on the colon BLM. In this context, the observed down-regulation (Fig. 3(a)–(d)) in the PCFT and the RFC mRNA corresponds to the reduced protein expression at colon BLM in ethanol-fed rats. This decrease in folate uptake in association with the down-regulation of the folate transporters in the rat colon is similar to the results of our earlier studies carried out in the small intestine(Reference Hamid, Kaur and Mahmood16, Reference Hamid, Wani and Rana18) and kidneys(Reference Hamid and Kaur37, Reference Hamid and Kaur38), and might contribute to ethanol-induced folate deficiency. Moreover, the decreased folate content of colon tissue in ethanol-fed rats reflects reduced substrate availability for the transporters at the BLM under in vivo conditions and might also contribute to the colonic malabsorption in chronic alcoholism. Although we have observed a reduced folate transport across the colonic BLM in ethanol-fed rats, a substantial amount of uptake still takes place during chronic alcoholism. This might be due to the associated passive diffusion component of the transport process along with the carrier-mediated transport. An earlier study(Reference Yang, Peterson and Sirotnak39) carried out in L1210 leukaemia cells has shown that 20 % of the total methotrexate uptake was contributed by passive diffusion; whether ethanol feeding affects this passive diffusion of 5-methyltetrahydrofolate under our experimental set is not known and is yet to be determined.
In the plane of basolateral membranes, LR could act as platforms modulating the protein activity by accumulating active pools of the transporters(Reference Anderson and Jacobson31). Proteins might enter LR at the golgi level and their shuttling between the golgi and cell membranes allows the cells to exert regulatory control over the surface expression of their proteins. Utilising the Optiprep floatation, we found that folate transporter proteins – PCFT and RFC – were present in the floating fractions corresponding to lipid raft microdomains of colon basolateral membranes. Our findings demonstrated the presence of PCFT and RFC in LR of the colon membranes of rats, which might be due to alteration in the lipid composition of biological membranes by alcohol(Reference Kaur, Kaur and Gupta40).
The immunohistochemical localisation of colon shows the localisation of both the folate transporters to the BBM as well as in the basolateral membrane surfaces, confirming the immunoblot experiment which demonstrated the expression of PCFT and RFC on both the BBM and BLM of colon. Moreover, less staining in the case of ethanol-fed rats suggests the decreased expression of PCFT and RFC.
In conclusion, these findings demonstrate that the decreased colon folate transport in chronic alcoholism may be attributed to decreased affinity and the number of folate transporter molecules across the colon BLM surfaces. Folate transport is carrier-mediated saturable, energy-independent, pH-dependent with the major involvement of RFC in folate exit across colon basolateral membrane with minimal involvement from PCFT. The decrease in uptake was associated with down-regulation of folate transporters and lipid raft associated reduction in levels of these transporters in colon BLM. The consequence of reduced folate transport across CAM results in reduced folate levels in colon.
The present study was supported by the financial grant sanctioned to J. K. from Council of Scientific and Industrial Research, New Delhi, India. N. A. W. carried out the animal study, transport study, prepared BLMV from animals for gene expression analyses, Western blotting and performed the statistical analysis and helped in the writing of the manuscript. A. H. carried out RT-PCR, Western blotting. K. L. K. was instrumental in designing the experiments involving radioisotopes and provided the facility for carrying out radioassays. J. K. conceived the study and participated in its design and coordination. The authors declare that there are no potential conflicts of interest. All the authors read and approved the final manuscript.