Abstract
Claudins are key functional and structural components of tight junctions (TJs) in epithelial cell sheets. The C-terminal fragment of Clostridium perfringens enterotoxin (C-CPE) binds to claudin-4 and reversibly modulates intestinal TJ seals, thereby enhancing paracellular transport of solutes. However, the use of C-CPE as an absorption enhancer is limited by the molecule’s immunogenicity and manufacturing cost. Here, we developed a high-throughput screening system based on the Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) method to identify claudin-4 binders in a library collection of 32,560 compounds. Thiostrepton, identified from the screen, decreased transepithelial electrical resistance and increased flux of 4-kDa fluorescein isothiocyanate–labelled dextran (FD-4) in Caco-2 cell monolayers, a model of intestinal epithelium. Thiostrepton changed the expression, but not the localisation, of TJ components. Treatment of rat jejunum with thiostrepton increased the absorption of FD-4 without tissue toxicity, indicating that thiostrepton is a novel claudin-4 binder that enhances intestinal permeability. The screening system may therefore be a useful tool for identifying claudin-4 binders to enhance drug absorption in mucosa.
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Introduction
Biopharmaceuticals, including peptides, proteins, antibodies and nucleic acids, play pivotal roles in the development of new drugs with breakthrough effects. The proportion of the drug market occupied by biopharmaceuticals is increasing yearly. Currently, biopharmaceuticals are administered primarily by injection, despite the pain and potential adverse effects (e.g., anaphylaxis) associated with this route. Therefore, the development of biopharmaceuticals that can be given through oral, nasal, pulmonary or percutaneous administration is required to avoid the risks of injection. However, biopharmaceuticals show remarkably low rates of absorption through mucosal or cutaneous epithelium owing to their hydrophilicity and high molecular weight1, and we need to develop a method for increasing their absorption to ensure sufficient bioavailability2.
Tight junctions (TJs), which are formed in the interstices between adjacent epithelial cells, seal the paracellular space to restrict the passage of solutes through the epithelial cell sheet3,4. Because TJs limit drug permeation through paracellular spaces, regulating TJ seals is an efficacious strategy for improving drug absorption5. A variety of substances controlling paracellular permeability have been developed5,6,7,8,9,10,11,12, and several of these bind claudin, a major component of the TJ barrier13,14. One of the most efficient is the C-terminal fragment of Clostridium perfringens enterotoxin (C-CPE), which binds to claudin-4 and can reversibly weaken the TJ barrier15. In rats, C-CPE increases the jejunal absorption of 4-kDa dextran (FD-4) by 400-fold over that of the currently used clinical absorption enhancer, sodium caprate8. Furthermore, C-CPE promotes the absorption of human parathyroid hormone, not only via the intestine, but also via the nasal and pulmonary routes16. Therefore, modulation of claudin-4 is a promising strategy for enhancing drug absorption by the paracellular permeation route. However, C-CPE is derived from a toxin fragment, and its immunogenicity may increase with multiple administrations17. In addition, it is desirable to develop a low-molecular–weight claudin binder that can be mass-produced at a low cost.
Here, we constructed a high-throughput screening system based on the Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) method for identifying claudin-4 binders to regulate mucosal TJ-barrier function18. We then used a TR-FRET–based assay to screen 32,560 compounds. The screen identified thiostrepton as a novel claudin-4 binder that attenuates TJ-barrier function in vitro and in vivo. We expect that the TR-FRET–based screening assay will be useful for identifying compounds that modulate the permeability of the mucosal epithelial barrier.
Results
Preparation of detection assay for claudin-4 and C-CPE interaction by TR-FRET
C-CPE is highly active in lowering TJ barrier function, suggesting that (a) the region of interaction between C-CPE and claudin-4 is pivotal in the disruption of claudin-4-mediated TJ barrier formation; and (b) interactions between other claudin-4 binders and this region have the potential to disrupt TJ barriers and enhance absorption via the paracellular route. To construct a detection system for interaction between claudin-4 and C-CPE, we prepared purified His (polyhistidine)-tagged claudin-4 (His-claudin-4) and GST (glutathione-S-transferase)-tagged C-CPE (GST-C-CPE) (Supplementary Figure 1) and performed an ELISA to confirm the interaction between His-claudin-4 and GST-C-CPE. By using a range of concentrations of GST-C-CPE, a dose-dependent signal was observed; in contrast, the negative control GST-C-CPE Y306A/L315A showed negligible affinity for claudin-419 (Supplementary Figure 2), indicating that His-claudin-4 interacted with GST-C-CPE.
We then developed a novel TR-FRET-based binding assay to detect interaction between claudin-4 and C-CPE. In this assay, europium (K)-conjugated-anti-His- antibody (Eu(K)-anti-His Ab), which binds to His-claudin-4, is used as a donor, and XL-665-conjugated-anti-GST–antibody (XL-665-anti-GST Ab), which binds to GST-C-CPE, is used as an acceptor. The formation of a quaternary complex containing Eu(K)-anti-His Ab, XL-665-anti-GST Ab, His-claudin-4, and GST-C-CPE results in fluorescence energy transfer between donor and acceptor. A binder inhibiting the interaction between claudin-4 and C-CPE disrupts the energy transfer between the donor and acceptor, thus reducing the FRET signal (Fig. 1a). We observed that FRET signals increased after the addition of GST-C-CPE but not after the addition of the negative control C-CPE Y306A/L315A (Fig. 1b). Therefore, the assay successfully detected the interaction of His-claudin-4 with GST-C-CPE. To assess whether the presence of another claudin-4 binder attenuated the FRET signal, we performed competition assays using C-CPEs and claudin-4 antibodies that bind to the C-terminal of claudin-4 (intracellular region) or extracellular domain of claudin-4 (extracellular region)12, respectively. The antibody recognising the extracellular domain of claudin-4 reduced TJ-barrier function12. Adding C-CPE or the antibody recognising the extracellular domain of claudin-4 considerably reduced the FRET signal, whereas adding C-CPE Y306A/L315A or the antibody recognising the C-terminal of claudin-4 did not affect the signals (Fig. 1c), indicating that this assay can be used to identify binders that bind to the extracellular domain of claudin-4.
TR-FRET assay for detecting interaction between claudin-4 and C-CPE. (a) Schematic representation of the TR-FRET-based assay for detecting the interaction between claudin-4 and C-CPE. When claudin-4 binder binds to the site of claudin-4 and C-CPE interaction, FRET signal is not detected. (b) Validation of the TR-FRET-based claudin-4 and C-CPE binding assay. The assay was performed by sequentially adding europium (K)-anti-His antibody (Ab), His-tagged claudin-4 (His-claudin-4) and XL665-anti-GST Ab, followed by the addition of GST-tagged C-CPE or C-CPE Y306A/L315A. TR-FRET signals were measured with an Artemis HTRF plate reader at 620 and 665 nm emission wavelengths. Data are means ± SD (n = 3). (c) Inhibitory effect of claudin-4 binders on the interaction between His-claudin-4 and GST-C-CPE in the TR-FRET-based assay. C-CPE, C-CPE Y306A/L315A or anti-claudin-4 Ab (either against the extracellular domain [ex] or the intracellular domain [in] of claudin 4) was incubated with His-claudin-4, and then GST-C-CPE, XL665-anti GST Ab and Eu(K)-anti His Ab were sequentially added. Data are means ± SD (n = 3).
TR-FRET–based screening assay for identification of claudin-4 binders
We optimised the TR-FRET assay for high-throughput screening by focusing on the concentrations of DMSO (dimethylsulfoxide), His-claudin-4, and GST-C-CPE and on the order of addition of compounds in the screening steps; changes in the DMSO concentration (0.1% to 2%) did not alter the FRET signals. The concentrations of C-CPE (2.5 to 10 nM) and claudin-4 (2.5 to 10 nM) that, when combined, yielded the highest FRET signal were each 10 nM. The number of procedural steps and final reaction time that achieved the optimal signal-to-background ratio and Z′-factor value were a 4-step assay and 30 min (Supplementary Figure 3).
We used the optimised protocol to screen a 32,560-compound library including (a) the Representative Diversity Set (20,000 compounds), (b) the Pharmacology Diversity set (10,240 compounds), and (c) the Spectrum Collection (2,320 compounds). The assay yielded excellent statistics: the mean Z′-factor was 0.86 ± 0.09, and the mean signal-to-background ratio was 6.9 ± 1.18 (Fig. 2a). The ‘hit’ cutoff was set at >60% inhibition of FRET signal, thus corresponding to 67 compounds. We then conducted a cytotoxicity assay of the hit compounds in human Caco-2 cells and identified 6 compounds with possible cytotoxicity. To determine whether the hit compounds bound directly to claudin-4 protein, not C-CPE, we performed Biacore analysis using recombinant human claudin-4 protein; 29 of the 67 compounds exhibited a Resonance Unit value of >3, thus indicating direct binding to claudin-4. Of the 29 compounds identified in our screen, 4 decreased the transepithelial electrical resistance (TER) value in a Caco-2 cell monolayer (Supplementary Figure 4). These results indicate that the claudin-4 binder screening system based on TR-FRET might be a useful tool for identifying claudin-4 binders with epithelial-barrier-disrupting activity.
Identification of thiostrepton as a claudin-4 binder. (a) Results of the TR-FRET-based high-throughput screening for claudin-4 binders. (b) Inhibition of the interaction between claudin-4 and C-CPE by thiostrepton in the TR-FRET assay. Thiostrepton was assayed in triplicate at various concentrations (1 nM to 10 μM) to assess its inhibitory effect. Data are means ± SD (n = 3). IC50, concentration at which the inhibitory response was reduced to 50%. (c) Competition assay of the interaction of thiostrepton with claudin-3 and claudin-4. Claudin-3- or claudin-4-expressing HT1080 cells (HT1080/CLDN3 or HT1080/CLDN4) and control (claudin non-expressing) HT1080 cells (HT1080/vector) were treated with vehicle alone, 10 µg/mL BSA or 10 µg/mL BSA plus 1 mM thiostrepton for 1 h. Then, FITC-conjugated C-CPE was added to the cells at 20 µg/mL for 1 h. The thiostrepton-bound cells were used for fluorescence-activated cell sorting analysis. Results for cells treated with vehicle alone are displayed in black. Results for cells treated with BSA with or without thiostrepton are displayed in grey or white, respectively.
Among the hit compounds, thiostrepton achieved the greatest attenuation of the barrier function of Caco-2 cells (Supplementary Figure 4). Thiostrepton inhibited the interaction between His-claudin-4 and GST-C-CPE at an IC50 (i.e. the concentration at which interaction is reduced by 50%) of 1.017 µM (Fig. 2b). Biacore analysis of the interaction between claudin-4 and thiostrepton revealed a KD of 6.615 × 10−6 (Supplementary Figure 5). In contrast, thiostrepton did not bind to C-CPE. To investigate whether thiostrepton prevents C-CPE from binding to claudins on the cell membrane, we conducted a competition assay. Thiostrepton inhibited the binding of C-CPE to claudin-4 on the cell membrane (Fig. 2c). Thiostrepton also inhibited the interaction between C-CPE and claudin-3, but this effect was substantially weaker than that for claudin-4. These results suggest that thiostrepton preferentially binds to claudin-4 on the cell membrane.
Thiostrepton attenuates the barrier function of the intestinal epithelial cell monolayer
Thiostrepton is an antibiotic derived from several strains of streptomycetes20, but its influence on the TJ barrier is unclear. Therefore, to examine the effect of thiostrepton on the barrier function of epithelial cell monolayers, we treated Caco-2 cells with thiostrepton. Thiostrepton (1–100 µM) reversibly decreased the TER value of Caco-2 cells in a time- and dose-dependent manner (Fig. 3a). We next investigated the effect of thiostrepton on the paracellular permeability of Caco-2 cells by using a paracellular tracer flux assay, with 4-kDa fluorescein isothiocyanate (FITC)–labelled dextran (FD-4) as the tracer. Caco-2 cells were treated with thiostrepton for 24 h, after which we measured the amount of FD-4 that had passed from the apical side to the basal side. Consistent with the TER decrease, thiostrepton (1–100 µM) treatment induced a dose-dependent increase in the paracellular flux of FD-4 (Fig. 3b). Furthermore, thiostrepton was not cytotoxic to Caco-2 cells in the concentration range of 1–100 µM (Fig. 3c). These results indicate that thiostrepton attenuated the TJ-barrier function of Caco-2 cell monolayers.
Effect of thiostrepton on the epithelial barrier in a Caco-2 cell monolayer. Caco-2 cell monolayers were incubated with vehicle or 1, 10, or 100 µM thiostrepton. (a) After 24 h, the media were replaced with fresh medium, and the cells were cultured for an additional 24 h. TER values were monitored at 12, 18, 24 and 48 h; TER values are shown as a percentage of the TER value at 0 h. Data are means ± SD (n = 3). (b) The permeability for 4-kDa FITC–dextran was measured at 24 h. Data are means ± SD (n = 3). *P < 0.05 vs vehicle-treated group, as determined by using Dunnett’s test. (c) The viability of cells treated with thiostrepton for 24 h was assessed by measuring the level of lactate dehydrogenase (LDH) released into the culture medium. Tween 20 (0.2%) served as the positive control. LDH release is shown as a percentage of the amount released by the vehicle-treated cells. Data are means ± SD (n = 3).
Effect of thiostrepton on TJ proteins
To investigate the effect of thiostrepton on TJ components of Caco-2 cells, we separated the 1% Triton-X-soluble and -insoluble fractions and performed immunoblotting and qRT-PCR analyses of cell–cell adhesion molecules. Thiostrepton treatment significantly decreased the 1% Triton-X-soluble protein and mRNA levels of claudin-1 and claudin-3 (Fig. 4a–c and Supplementary Figure 6), whereas the protein levels in the 1% Triton-X-insoluble fraction were unchanged. In contrast, thiostrepton treatment increased the 1% Triton-X-soluble protein and mRNA levels, and the 1% Triton-X-insoluble protein levels, of claudin-4. Immunofluorescence staining showed that thiostrepton treatment did not alter the cellular localisation of claudin-1, claudin-4, occludin or ZO-1 (Fig. 4d). To evaluate the effect of thiostrepton on the paracellular permeation of molecules, we used sulfo-NHS-SS-biotin (607 Da), which is a cell-membrane-impermeable molecule21,22. When Caco-2 cell monolayers were treated with thiostrepton and then apically incubated with the biotin compound, biotin signal was detected within the paracellular space; in contrast, no biotin permeation was observed in untreated control cultures (Fig. 5). The signal in the control cultures was due to residual biotin that remained on the apical side after washing; it was not translocated biotin. These results suggest that thiostrepton attenuates TJ-barrier function without distinct changes in the localisation of the TJ components.
Thiostrepton effect on tight junction components of Caco-2 cell monolayers. Caco-2 cell monolayers were incubated with vehicle or 1, 10 or 100 µM thiostrepton. Triton-X (1%)-soluble and -insoluble lysates were collected and immunoblotted for claudin-1 (CLDN1), claudin-3 (CLDN3) or claudin-4 (CLDN4) (a). β-actin served as the loading control. Pre-cropped blots are included in Supplementary Figure 6. Relative protein density was calculated as the ratio of the protein density to the density in the vehicle control (b). Data are means ± SD (n = 3). *P < 0.05 vs. vehicle-treated group, as determined by using Dunnett’s test. (c) Caco-2 cells were treated with or without 100 µM thiostrepton for 24 h, and then cell lysates were subjected to qRT-PCR analysis for CLDN1, CLDN3, or CLDN4. Data are means ± SD (n = 3). *P < 0.05 vs vehicle-treated group, as determined by using Dunnett’s test. (d) Immunofluorescence localisation of CLDN1, CLDN4, occludin (OCLN) and ZO-1 after treatment with 100 µM thiostrepton or no treatment for 24 h. Bar = 10 µm.
Thiostrepton effect on paracellular tracer permeability. Caco-2 cell monolayers were treated with 100 µM thiostrepton or left untreated (control) and then apically incubated with sulfo-NHS-SS-biotin (606.7 Da; red) and counterstained with anti-ZO-1 antibody (green; TJ stain) and DAPI (blue; nuclear stain). Scanning of the lateral (z-) axis of the cells showed specific localisation of the biotin signals (red) within intercellular contacts, whereas no biotin permeation was observed in control cells. Bar = 10 µm.
Thiostrepton enhances intestinal absorption of a macromolecule
To investigate the effect of thiostrepton on the jejunal absorption of a macromolecule, we conducted an in situ loop assay, using FD-4 as the macro-tracer molecule. Thiostrepton enhanced rat jejunal absorption of FD-4 in a dose-dependent manner, as compared with that in the vehicle-treated group (Fig. 6a and b). In addition, thiostrepton treatment increased plasma FD-4 concentrations, which reached a maximum of 0.6 µg/mL. Histochemical analysis showed no evidence of intestinal tissue toxicity (Fig. 6c and Supplementary Figure 7). These results indicate that thiostrepton has the potential to enhance the intestinal absorption of macromolecules without intestinal toxicity.
Mucosal absorption-enhancing effect of thiostrepton. (a) Rat jejunum was treated with vehicle alone or with 0.1 or 1 mM thiostrepton and 1 mg 4-kDa FITC-labelled dextran (FD-4). Time-course changes in plasma FD-4 concentration were monitored, and the area under the time–concentration curve between 0 and 6 h (AUC0–6 h) was calculated (b). Data are means ± SD (n = 4). *P < 0.05 vs vehicle-treated group, as determined by using Dunnett’s test. (c) Histological analysis of representative thiostrepton-treated rat jejunum. After 6 h of treatment with vehicle or thiostrepton (0.1 or 1 mM), the jejunum was fixed and stained with haematoxylin and eosin.
Discussion
Although several claudin-4 binders have been reported23,24,25, C-CPE and its variants are the most commonly reported claudin-4 binders known to regulate TJ barrier function8,26,27,28. C-CPE has the potential to enhance the absorption of macromolecule-like peptides in various mucosal tissues16,29. Therefore, modulation of claudin-4-based TJ-barrier function is a promising strategy for develo** an absorption enhancer. However, a screening system for identifying claudin binders that might regulate TJ-barrier function had not been developed previously. Here, we constructed a claudin-4 binder screening system based on TR-FRET, which detects the interaction between claudin-4 and C-CPE. We surmise that our novel screening system will not only simplify the identification of compounds binding to claudin-4 but will also restrict the outcome to compounds with TJ barrier-regulating activity, given that the compounds obtained bind substantially to the claudin-4 region that interacts with C-CPE. In fact, we showed that TR-FRET analysis distinguished between an antibody that recognises the intracellular domain of claudin-4, which cannot regulate TJ barriers, and one that recognises the extracellular domain of claudin-4, which attenuates TJ-barrier function. By using this system, we successfully identified novel claudin-4 binders that attenuated epithelial barrier function. Among them, thiostrepton strongly attenuated the TJ-barrier function of Caco-2 cell monolayers. Furthermore, we demonstrated that thiostrepton enhanced rat jejunal absorption of a macromolecule without tissue toxicity. Therefore, our screening system is appropriate for identifying TJ-modulating claudin-4 binders.
Thiostrepton is a veterinary antibiotic used to treat dermatological diseases and mastitis caused by Gram-negative bacteria50.
Immunofluorescence staining
Localisation of claudins-1 and -4, occludin and ZO-1 on Caco-2 cells was assessed by immunofluorescence microscopy. Caco-2 cells were seeded on Transwell filters (diameter, 12 mm; pore size, 0.4 µm; Corning). After treatment with thiostrepton (100 µM) or no treatment for 24 h, the Caco-2 cells were fixed with methanol–acetone (1:1 v/v) for 5 min and then permeabilised with 0.2% Triton X-100 in PBS for 10 min. After non-specific binding had been blocked by incubation with 1% BSA in TBS buffer (20 mM Tris-HCl, pH 7.4, 40 mM NaCl) containing 0.05% Tween-20 (T-TBS) for 1 h, the cells were incubated with anti-claudin-1, -claudin-4, -occludin and -ZO-1 antibodies in 1% BSA in T-TBS for 1 h. After incubation of the cells with fluorescent secondary antibodies for 1 h, the immunofluorescence images were observed under an immunofluorescence microscope (Keyence, Tokyo, Japan). For visualisation of biotin passing through the TJ, Caco-2 cells treated with 100 µM thiostrepton or left untreated were apically labelled with sulfo-NHS-SS-biotin (606.7 Da) for 10 min. The cells were then fixed, and anti-ZO-1 antibody and 4,6-diamidino-2-phenylindole dihydrochloride (DAPI) were employed for immunofluorescence staining of the TJ or nucleus, respectively.
In situ loop assay
All procedures involving mice and experimental protocols were approved by the Ethics Committee of Osaka University (permission no. 27-5-2). Rat jejunal absorption of FD-4 was evaluated by using an in situ loop assay. After 7-week-old Wister male rats were anesthetised, a midline abdominal incision was made and the jejunum was washed with PBS. A 5-cm-long jejunal loop was prepared and both ends were closed with sutures. A mixture of 1 mg FD-4 and 0.1 or 1 µM thiostrepton in 100 µL was injected into the jejunal loop. Blood was collected at the time points indicated. Plasma levels of FD-4 were measured with a TriStar LB 941 microplate reader (Berthold Technologies). The area under the plasma concentration curve of the FD-4 from 0 to 6 h was calculated by using the trapezoidal method. Recovered intestinal tissues were stained with haematoxylin and eosin and examined for tissue toxicity.
Statistical analysis
Data are presented as means ± 1 SD. Dunnett’s test was used for statistical analyses. A P value of less than 0.05 was considered indicative of statistical significance.
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Acknowledgements
We thank Yasue Matsunaga and Kazuto Nunomura for their technical assistance in TR-FRET screening and Kaori Ikuma and Shizuka Yamagishi for their technical assistance in animal experiments. This work was supported by JSPS KAKENHI Grant No. 16K08370; by the Yokoyama Rinsho Yakuri Foundation; by the Research Foundation for Pharmaceutical Sciences; by the Takeda Science Foundation; by the Platform for Drug Discovery, Informatics and Structural Life Science of the Ministry of Education, Culture, Sports, Science and Technology, Japan; and by the Basic Science and Platform Technology Program for innovative Biological Medicine from AMED.
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A.W., K.Y. and M.K. designed the research. K.M., H.S., N.K. and T.T. provided materials. A.W., M.K., Y.S., K.H., Y.Y. and H.T. performed the experiments. A.W., M.K., H.T., K.Y. and M.K. analysed the data; A.W. and M.K. wrote the paper. All authors analysed the results and approved the final version of the manuscript.
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Watari, A., Kodaka, M., Matsuhisa, K. et al. Identification of claudin-4 binder that attenuates tight junction barrier function by TR-FRET-based screening assay. Sci Rep 7, 14514 (2017). https://doi.org/10.1038/s41598-017-15108-y
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DOI: https://doi.org/10.1038/s41598-017-15108-y
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