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  • Bafilomycin A1 br Gene silencing by RNA interference br AsPC


    2.6. Gene silencing by RNA interference
    AsPC-1 Bafilomycin A1
    were seeded at 1.0 105 cells/well on poly-D-lysine coated 24-well plates 24 hr prior to siRNA transfection. Negative control siRNA (SigmaeAldrich, MISSION siRNA Universal Negative Control #2), PEPT1 siRNA #1 (SigmaeAldrich, MISSIONsiRNA: Hs_SLC15A1_7227_s), and PEPT1 siRNA #2 (SigmaeAldrich, MIS-SIONsiRNA: Hs_SLC15A1_7228_s) were transfected with Lipofect-amine RNAiMAX (Invitrogen). The cells were used for analyses at 48 hr after transfection.
    2.7. Western blot analysis
    AsPC-1 cells (5.0 106 cells) mixed with the same volume of Matrigel (Corning, Corning, NY, USA) were subcutaneously injected into the back of BALB/c-nu/nu mice (female, 5-week-old). Mice were maintained as previously described.23 Three weeks after xenotransplantation, BPA-Tyr (370 mg/kg, dissolved in 200 mL of Bafilomycin A1 PBS) was intravenously injected. Mice were deeply anesthetized by inhaled approximately 2% isoflurane and dissected at 3 and 5 hr after BPA-Tyr administration. The collected blood and tissues were subjected to ICP-AES. The experiments were conducted according to the regulations of the Animal Care and Use Committee of Osaka University.
    2.9. Statistical analysis
    Unpaired Student t-test was used to compare two sets of data. One-way ANOVA with Dunnett's post-test was used for compari-sons of more than two sets of data. Differences were considered to be significant if the P-value was <0.05.
    3. Results
    3.1. Functional expression of oligopeptide transporters in stable cell lines
    The protein expression of PEPT1 and PEPT2 in the constructed stable cell lines (HEK293-PEPT1 and HEK293-PEPT2 cells) was confirmed by western blot analysis as shown in Fig. S1. The [3H]Gly-Sar uptake detected in both cell lines was considerably higher than that of MOCK cells (Fig. S1), indicating that PEPT1 and PEPT2 were functionally expressed. Uptakes of [3H]Gly-Sar almost linearly increased within 5 and 10 min of incubation time for PEPT1 and PEPT2, respectively. In all the subsequent inhibition and kinetic analyses, the uptake was measured for 5 min to determine the initial transport rates.  3.2. Interaction of BPA-Tyr and Tyr-BPA with oligopeptide transporters
    Inhibition experiments were carried out to examine whether the synthesized BPA-containing dipeptides interact with oligo-peptide transporters. The uptakes of [3H]Gly-Sar medicated by PEPT1 and PEPT2 were strongly inhibited by BPA-Tyr and Tyr-BPA (Fig. 2A, B). The inhibitory effect of BPA-containing di-peptides on the [3H]Gly-Sar uptake was concentration dependent (Fig. 2CeF). The IC50 values of BPA-Tyr to inhibit PEPT1- and PEPT2-mediated uptakes of [3H]Gly-Sar (10 mM) were deter-mined to be 112.7 ± 1.2 mM and 11.5 ± 1.2 mM, respectively. The IC50 values of Tyr-BPA for PEPT1- and PEPT2-mediated uptakes of [3H]Gly-Sar (10 mM) were 801.7 ± 1.6 mM and 49.0 ± 1.1 mM, respectively.
    To further characterize the inhibition profiles, the concentra-tion dependence of [3H]Gly-Sar uptakes in HEK293-PEPT1 and HEK293-PEPT2 cells was measured in the presence or absence of BPA-containing dipeptides to determine the Ki values (Fig. S2). Nonlinear regression analysis of the obtained results revealed that [3H]Gly-Sar uptakes mediated by PEPT1 and PEPT2 were competitively inhibited by BPA-containing dipeptides. Consis-tently, the double reciprocal plots indicated the apparent increase of Km in the presence of BPA-containing dipeptides without changing Vmax. The Ki values of BPA-Tyr and Tyr-BPA for PEPT1 and PEPT2 determined by nonlinear regression analysis are summa-rized in Table 1. For both PEPT1 and PEPT2, BPA-Tyr showed several times higher affinities compared with Tyr-BPA. Regarding the selectivity between the oligopeptide transporters, both BPA-Tyr and Tyr-BPA exhibited about 20e30-fold higher affinities for PEPT2 than for PEPT1.