Rmination of Protein Quantity of ASCT2 and B0ATThe frozen jejunum samples were powdered under liquid nitrogen, and lysed in RIPA buffer (150 mM NaCl, 1 Triton X100, 0.5 sodium deoxycholate, 0.1 SDS, 50 mM Tris-HCl at pH 7.4, plus a protease inhibitor cocktail purchased from Roche, Shanghai, China). After centrifugation at 10,0006g and 4uC for 10 min, protein concentration in the supernatant fluid was determined using the Bicinchoninic Acid assay (Beyotime Biotechnology, Haimen, China). All samples were adjusted to an equal protein concentration and then diluted with 26loading buffer (0.63 ml of 0.5 M Tris-HCl (pH 6.8), 0.42 ml 75 glycerol, 0.125 g sodium dodecyl sulfate (SDS), 0.25 ml b-mercaptoethanol, 0.2 ml 0.05 solution of bromphenol blue, and 1 ml water) to Table 1. Primers used for real-time PCR.TA1 (uC)Determination of AA Contents in Plasma, Liver and MusclePlasma AA contents were determined as previously described [24?5]. In brief, 1 ml of the plasma sample and 2.5 ml of 7.5 trichloracetic acid solution were mixed thoroughly and centrifuged at 12,0006g and 4uC for 15 min. The supernatant fluid was collected for analysis of AA by an ion-exchange AA analyzer (Tokyo, Japan). To measure the contents of AA in the muscle and liver, about 0.1 g freeze-dried muscle or liver tissue was ground and hydrolyzed in 10 mL of 6 mol/L HCl at 110uC for 24 h. The solution was then adjusted to the volume of 100 mL and then a 1 mL of the settled solution was used for further analysis after a 10-fold dilution. Plasma samples were filtered through a 0.45 mm membrane before analysis [26].Genes Slc1aPrimers Forward ReverseSequences (59-39) GATTGTGGAGATGGAGGATGTGG TGCGAGTGAAGAGGAAGTAGATGA GA TCTGTCCACAACAACTGCGAG CAGCGAAGTTCTCCTGCGTC AAGGAGTAAGAGCCCCTGGA TCTGGGATGGAAACTGGAASize (bp)Slc6a19 Forward Reverse GAPDH Forward Reverse1 TA, Annealing temperature. doi:10.1371/journal.pone.0050921.tNeutral Amino Acids in Mini-Pigletsa final volume of 2.5 ml and heated in boiling water for 5 min. After cooled on ice, the solution was used for Western blot analysis. Same amounts of sample aliquots (20 mg protein) were subjected to 10 SDS-PAGE (10 gradient gel) and were transferred to PVDF membranes (Millipore, MA, USA) overnight at 12 V using the Bio-Rad Transblot apparatus (CA, USA). The membranes were AVP chemical information blocked in 5 fat-free milk in Tris-Tween buffered saline (TTBS; 20 mM Tris/150 mM NaCl, pH 7.5, and 0.1 Tween20) for 3 h and then incubated with ASCT2, B0AT1 or b-actin antibody (Table 2) at 4oC overnight with gentle rocking. After washing three times with TTBS, the membranes were incubated at room temperature for 2 h with horseradish peroxidase-linked secondary antibodies (Santa Cruz, CA, USA). The secondary antibody were used at dilutions of 1:3,000. Finally, the membranes were washed with TTBS, followed by development using Supersignal West Dura Extended Duration Substrate according to the Naringin cost manufacturer’s instructions (Pierce, Rockford, IL). The images were detected on chemiluminescence (Applygen Technologies Inc., Beijing, China). Multiple exposures of each Western blot were performed to ensure linearity of chemiluminescence signals. Western blots were quantified by measuring the intensity of correctly sized bands using AlphaImager 2200 software (Alpha Innotech Corporation, CA, USA). The ratio of intensities of a studied protein band and housekeeping protein band 24272870 was calculated for each filter and the ratios from different Western blot filters were used f.Rmination of Protein Quantity of ASCT2 and B0ATThe frozen jejunum samples were powdered under liquid nitrogen, and lysed in RIPA buffer (150 mM NaCl, 1 Triton X100, 0.5 sodium deoxycholate, 0.1 SDS, 50 mM Tris-HCl at pH 7.4, plus a protease inhibitor cocktail purchased from Roche, Shanghai, China). After centrifugation at 10,0006g and 4uC for 10 min, protein concentration in the supernatant fluid was determined using the Bicinchoninic Acid assay (Beyotime Biotechnology, Haimen, China). All samples were adjusted to an equal protein concentration and then diluted with 26loading buffer (0.63 ml of 0.5 M Tris-HCl (pH 6.8), 0.42 ml 75 glycerol, 0.125 g sodium dodecyl sulfate (SDS), 0.25 ml b-mercaptoethanol, 0.2 ml 0.05 solution of bromphenol blue, and 1 ml water) to Table 1. Primers used for real-time PCR.TA1 (uC)Determination of AA Contents in Plasma, Liver and MusclePlasma AA contents were determined as previously described [24?5]. In brief, 1 ml of the plasma sample and 2.5 ml of 7.5 trichloracetic acid solution were mixed thoroughly and centrifuged at 12,0006g and 4uC for 15 min. The supernatant fluid was collected for analysis of AA by an ion-exchange AA analyzer (Tokyo, Japan). To measure the contents of AA in the muscle and liver, about 0.1 g freeze-dried muscle or liver tissue was ground and hydrolyzed in 10 mL of 6 mol/L HCl at 110uC for 24 h. The solution was then adjusted to the volume of 100 mL and then a 1 mL of the settled solution was used for further analysis after a 10-fold dilution. Plasma samples were filtered through a 0.45 mm membrane before analysis [26].Genes Slc1aPrimers Forward ReverseSequences (59-39) GATTGTGGAGATGGAGGATGTGG TGCGAGTGAAGAGGAAGTAGATGA GA TCTGTCCACAACAACTGCGAG CAGCGAAGTTCTCCTGCGTC AAGGAGTAAGAGCCCCTGGA TCTGGGATGGAAACTGGAASize (bp)Slc6a19 Forward Reverse GAPDH Forward Reverse1 TA, Annealing temperature. doi:10.1371/journal.pone.0050921.tNeutral Amino Acids in Mini-Pigletsa final volume of 2.5 ml and heated in boiling water for 5 min. After cooled on ice, the solution was used for Western blot analysis. Same amounts of sample aliquots (20 mg protein) were subjected to 10 SDS-PAGE (10 gradient gel) and were transferred to PVDF membranes (Millipore, MA, USA) overnight at 12 V using the Bio-Rad Transblot apparatus (CA, USA). The membranes were blocked in 5 fat-free milk in Tris-Tween buffered saline (TTBS; 20 mM Tris/150 mM NaCl, pH 7.5, and 0.1 Tween20) for 3 h and then incubated with ASCT2, B0AT1 or b-actin antibody (Table 2) at 4oC overnight with gentle rocking. After washing three times with TTBS, the membranes were incubated at room temperature for 2 h with horseradish peroxidase-linked secondary antibodies (Santa Cruz, CA, USA). The secondary antibody were used at dilutions of 1:3,000. Finally, the membranes were washed with TTBS, followed by development using Supersignal West Dura Extended Duration Substrate according to the manufacturer’s instructions (Pierce, Rockford, IL). The images were detected on chemiluminescence (Applygen Technologies Inc., Beijing, China). Multiple exposures of each Western blot were performed to ensure linearity of chemiluminescence signals. Western blots were quantified by measuring the intensity of correctly sized bands using AlphaImager 2200 software (Alpha Innotech Corporation, CA, USA). The ratio of intensities of a studied protein band and housekeeping protein band 24272870 was calculated for each filter and the ratios from different Western blot filters were used f.
