AGR2 ameliorates tumor necrosis factor-α-induced epithelial barrier dysfunction via suppression of NF-κB p65-mediated MLCK/p-MLC pathway activation.

Intestinal epithelial barrier dysfunction plays a critical role in the pathogenesis of inflammatory bowel disease (IBD). Anterior gradient protein 2 homologue (AGR2) assists in maintaining intestinal homeostasis in dextran sulphate sodium-induced mouse ileocolitis; however, it is unclear whether it modulates intestinal barrier function. Our study aimed to investigate the protective role of AGR2 in tumor necrosis factor (TNF)-α-induced intestinal epithelial barrier injury. Caco-2 cell monolayers were pre-transfected with an AGR2 plasmid and then exposed to TNF-α. Epithelial permeability was assessed by detecting transepithelial electrical resistance and fluorescein isothiocyanate-dextran (40 kDa) flux. The protein expression levels of zonula occludens-1 (ZO-1), occludin, claudin-1, myosin light chain kinase (MLCK)/p-MLC, and nuclear factor (NF)-κB p65 were determined by western blotting. In addition, the cellular distributions of ZO-1, occludin, F-actin, and NF-κB p65 were evaluated by immunofluorescence staining. The results showed that the AGR2 mRNA and protein expression levels were both decreased in the Caco-2 cell monolayers, while AGR2 overexpression significantly ameliorated TNF-α-induced epithelial barrier hyperpermeability, increased the expression of tight junction (TJ) proteins and stabilized the cytoskeletal structure. Furthermore, AGR2 inhibited the changes in MLCK, MLC and p-MLC expression in response to TNF-α stimulation. Collectively, our study suggests that AGR2 inhibits TNF-α‑induced Caco-2 cell hyperpermeability by regulating TJ and that this protective mechanism may be promoted by inhibition of NF-κB p65-mediated activation of the MLCK/p-MLC signaling pathway.

Introduction

Disruption of intestinal epithelial barrier function is a key characteristic of inflammatory bowel disease (IBD) (1–4). An intact intestinal epithelial barrier is essential for defending against the invasion of antigens and for maintaining the internal environment, which separates luminal contents within the body and prevents luminal bacterial and microbial translocation. Intestinal barrier dysfunction leads to entry of intestinal bacteria into the body, causing local or systemic inflammatory responses (5,6). Repair of the intestinal mucosa has become a standard criterion for evaluating the efficacy of IBD treatments (7). Therefore, effective maintenance of intestinal epithelial barrier function is of great importance in IBD.

Integrity of the intestinal epithelial barrier depends on a complex network of intercellular tight junctions (TJs) and cytoskeletal structures, and disruption of this network results in impaired barrier function (8–11). TJ proteins are located at the apical ends of epithelial cells, which contain both transmembrane (e.g., occludin, claudin and junctional adhesion molecules) and cytoplasmic zonula occludens (ZO) proteins. As the determinant of epithelial permeability, TJ proteins are the most important component of the epithelial mucosal barrier (12,13). Damage to intestinal epithelial TJs leads to increased intercellular permeability, allowing for bacteria and endotoxins to penetrate the mucosa and enter into circulation, resulting in severe inflammatory responses (14,15). Rearrangement and redistribution of cytoskeletal F-actin also leads to changes in intestinal epithelial barrier permeability (16).

Tumor necrosis factor (TNF)-α is a multifunctional proinflammatory cytokine which participates in the pathogenesis of IBD (17). TNF-α is associated with damage to intestinal TJs and cytoskeletal rearrangements, which lead to increased intestinal permeability. It also promotes release of the inflammatory factors interleukin (IL)-8, IL-17 and interferon (IFN)-γ (18–20). Both the myosin light chain kinase (MLCK)/p-MLC pathway and nuclear factor (NF)-κB activation have key roles in TNF-α-mediated damage to the intestinal barrier (21,22). Activation of the MLCK/p-MLC pathway leads to upregulation of the expression of TJ proteins, alterations in cell adhesion and migration, and cytoskeletal rearrangements (16,23,24).

Anterior gradient protein 2 homologue (AGR2) is a member of the protein disulphide isomerase family that plays an important role in maintaining intestinal homeostasis in IBD (25). The prevalence of AGR2 gene mutations is higher in patients with IBD than in the general population (26). In animal models of IBD, AGR2 has been shown to maintain homeostatic functions in intestinal Paneth and goblet cells (27), and AGR2-knockout mice have been reported to be susceptible to the development of severe ileocolitis (28). Thus, AGR2 is essential for maintaining the intestinal epithelial cell function in IBD, but it is unclear whether it regulates intestinal epithelial barrier function.

Therefore, we investigated the roles of AGR2 in epithelial permeability, TJ protein expression, and cytoskeletal structure. Furthermore, we evaluated the mechanism by which AGR2 ameliorates TNF-α-mediated damage to the intestinal barrier.

Materials and methods

Cell culture and preparation

Caco-2 cells were purchased from the Chinese Academy of Sciences (Shanghai, China). The cells were cultured in RPMI-1640 medium containing 10% fetal bovine serum (FBS; ScienCell Research Laboratories, San Diego, CA, USA) at 37°C in 5% CO2. For the monolayer model, cells were plated at 3×104/ml onto Transwell filters with a 0.4-μm pore size (Millipore, Billerica, MA, USA) and cultured for 21 to 28 days prior to the experiments. The culture medium was changed every 2 days. The experimental monolayers were pre-transfected with an AGR2 plasmid and were then stimulated with 100 ng/ml rhTNF-α for 48 h.

Plasmid construction and transfection

A pcDNA3.1 eukaryotic expression vector carrying the human AGR2 gene was constructed. Cells were transfected with either a pcDNA3.1-AGR2 plasmid or a pcDNA3.1 vector control plasmid. For transfection, the cells were incubated in 100 μl Opti-MEM medium containing 8 μl Lipofectamine 2000 (both from Invitrogen Life Technologies, Carlsbad, CA, USA) for 5 min, followed by the addition of 2 μg plasmids and incubation for another 20 min. The mixtures were then transferred to 6-well plates and cultured for 4 h. Subsequently, the transfection medium was substituted with culture medium, and the transfected cells were cultured at 37°C in 5% CO2.

Determination of transepithelial electrical resistance (TEER)

Caco-2 cells were seeded onto Transwell chambers, and epithelial permeability was assessed by evaluating TEER using a Millicell ERS-2 Voltohmmeter (Millipore). Two wells containing only culture medium were used as blank controls. Measurements were carried out at a constant temperature at three different locations within each chamber. The mean value of three consecutive measurements was used to calculate TEER.

TEER (Ω · cm2) = (measured TEER - control TEER) × effective membrane area of the cell culture well.

Measurement of paracellular marker fluorescein isothiocyanate (FITC)-dextran 40 (FD-40) (40 kDa) flux

The monolayers were washed with HBSS, and the RPMI-1640 medium in the apical chambers was replaced with FITC-conjugated dextran (80 μg/ml, 40 kDa; Sigma-Aldrich, St. Louis, MO, USA) in HBSS. The monolayers were incubated at 37°C for 1 h. Then, the fluorescence of the culture medium in the lower chambers was detected with a fluorescence plate reader (Varioskan Flash; Thermo Electron Corporation, Vantaa, Finland) at excitation and emission wavelengths of 427 and 536 nm, respectively. Fluorescein concentrations were determined by comparison to a standard curve.

Fluorescence transmittance (%) = FITC-dextran concentration in the lower chamber/FITC-dextran concentration added to the upper chamber × 100.

Quantitative (real-time) PCR (qPCR)

TRIzol was utilized to extract total RNA from the cells, and reserve transcription was carried out using a PrimeScript RT reagent kit (Takara Bio Inc., Shiga, Japan). qPCR was performed using a SYBR Premix Ex kit (Takara Bio Inc.) and a Bio-Rad iQ5 Real-Time system (Bio-Rad Laboratories, Inc., Hercules, CA, USA). The primers for this study were as follows: β-actin forward, 5′-CTTAGTTGCGTTACACCCTTTCTTG-3′ and reverse, 5′-CTGTCACCTTCACCGTTCCAGTTT-3′; AGR2 forward, 5′-GCATTCTTGCTCCTTGTGG-3′ and reverse, 5′-GACTGTGTGGGCACTCATCC-3′. Expression levels were calculated using the 2−ΔΔCT method.

Western blotting

Radioimmunoprecipitation assay (RIPA) and phenylmethanesulfonyl fluoride (PMSF) lysate buffers were used to extract total protein from the Caco-2 cells. The protein concentrations of the extracted samples were determined by bicinchoninic acid assay. These concentrations were adjusted by addition of distilled water. Equal volumes of sample buffer and boiling water were mixed, and the mixtures were boiled for 5 min to denature the proteins. Equal amounts of proteins (40 μg) for each sample were loaded onto SDS-PAGE gels for electrophoresis, and then transferred to PVDF membranes and blocked by 5% non-fat milk for 1 h. Next, incubation was carried out with the primary antibodies, including anti-AGR2 (ab76473; 1:3,000), anti-ZO-1 (ab59720; 1:500), anti-claudin-1 (ab15098; 1:500), anti-occludin (ab31721; 1:500) anti-MLCK (ab76092; 1:5,000) and anti-NF-κB (ab207297; 1:500) (all from Abcam, Cambridge, MA, USA), anti-p-MLC (#3671; 1:750) and anti-MLC (#8505; 1:750) (both from Cell Signaling Technology, Inc., Danvers, MA, USA) and anti-β-actin (20536-1-AP; 1:2,000; Proteintech, Wuhan, China) overnight at 4°C. After that, incubation was carried out with horseradish peroxidase (HRP)-conjugated secondary antibodies (SA00001-2; 1:5,000; Proteintech) for 2 h and visualized by electrochemiluminescence (ECL). Protein bands were detected using Gel-Pro Analyser 4.0 (Media Cybernetics, Inc., Rockville, MD, USA).

Immunofluorescence staining

Caco-2 monolayers were pre-transfected with AGR2 gene plasmids or a control plasmid vector; after 24 h, 100 ng/ml TNF-α was added. After 48 h of TNF-α exposure, the cultures were fixed with 4% polyformaldehyde for 15 min and then incubated with 0.5% Triton X-100 for 30 min. Subsequently, the cultures were incubated with goat serum for 15 min. After that, the cells were incubated with primary antibodies including anti-F-actin (ab205; 1:100), anti-ZO-1 (1:200), anti-occludin (1:100) and anti-NF-κB p65 (1:200) (all from Abcam) overnight at 4°C. Next, they were incubated with a fluorescent-labelled goat anti-rabbit IgG (H+L) secondary antibody (SA00003-1; 1:200; Proteintech) for 1 h at room temperature. After nuclear counterstaining of the cells with 4′,6-diamidino-2-phenylindole (DAPI) (Life Technologies, Thermo Fisher Scientific, Inc., Waltham, MA, USA), images were captured by laser scanning fluorescence microscopy (TCS SP5; Leica Microsystems, Wetzlar, Germany) at ×400 magnification.

Statistical analysis

Assays were performed at least in triplicate, and the results were reported as the mean ± SD. The significance of differences was assessed by analysis of variance (ANOVA) or the t-test using SPSS version 21.0 software (SPSS, Inc., Chicago, IL, USA). A P<0.05 was considered statistically significant.

Results

TNF-α decreases AGR2 expression in confluent monolayers of cultured intestinal epithelial cells

Caco-2 cell cultures reached confluence by day 21, forming monolayers consisting of irregular polygonal cells with a cobblestone appearance and intercellular TJs, as observed by light micro scopy. TEER remained stable at >600 Ω/cm2, indicating the successful establishment of the in vitro intestinal epithelial barrier model. TNF-α (100 ng/ml) was then added to the model cultures, and after 48 h, the expression level of AGR2 was detected. Both the AGR2 mRNA and protein expression levels were obviously decreased by TNF-α exposure compared with the levels in the untreated control monolayers (Fig. 1A and B).

Figure 1

(A) Anterior gradient protein 2 homologue (AGR2) mRNA expression was significantly reduced in the rhTNF-α-induced intestinal epithelial barrier injury model. (B) AGR2 protein expression was also decreased by rhTNF-α. The results are presented as the mean ± SD. **P<0.01 compared with the controls.

Construction of an AGR2 overexpression model by transfection of an AGR2 or control plasmid

AGR2 or control plasmid vectors were transfected in vitro into Caco-2 cell monolayers, and AGR2 mRNA expression was determined by qRT-PCR after 24 h. After another 48 h of culturing, AGR2 protein expression was measured by western blotting and compared with that in the controls. The results showed that both the AGR2 mRNA and protein expression levels were significantly increased in the Caco-2 cells transfected with the AGR2 plasmids (Fig. 2A and B). These findings indicate the successful construction of the AGR2 plasmid.

Figure 2

Both anterior gradient protein 2 homologue (AGR2) mRNA expression (A) and (B) protein expression were significantly higher in Caco-2 cells transfected with the AGR2 plasmids than in the control cells. The results are presented as the mean ± SD. **P<0.01 compared with the control group.

AGR2 reduces TNF-α-induced increase in permeability of intestinal epithelial cell monolayers

Caco-2 cell monolayers were transfected with AGR2 or control plasmids, and after incubation for 24 h, 100 ng/ml TNF-α was added. Permeability of the intestinal epithelial cell monolayers was assessed by measuring TEER and FD-40 flux after 48 h of incubation with TNF-α. The results showed that TEER was significantly lower and FD-40 flux was significantly higher in the TNF-α-stimulated monolayers compared with that noted in the control monolayers (Fig. 3A and B). AGR2 plasmid transfection significantly inhibited the decrease in TEER as well as the increase in FD-40 flux induced by TNF-α (Fig. 3A and B), indicating that AGR2 ameliorated the TNF-α-induced increase in permeability of the model system.

Figure 3

(A) Anterior gradient protein 2 homologue (AGR2) plasmid transfection significantly inhibited the decrease in transepithelial electrical resistance (TEER) induced by rhTNF-α. (B) AGR2 plasmid transfection significantly inhibited the increase in fluorescein isothiocyanate (FITC)-dextran (40 kDa) flux (FD-40) induced by rhTNF-α. The results are presented as the mean ± SD. **P<0.01 compared with the control group; ##P<0.01 compared with the TNF-α group.

AGR2 inhibits the decreased expression of ZO-1, occludin, and claudin-1 TJ proteins induced by TNF-α

Disruption of TJs is an important component of altered intestinal epithelial barrier function (29). We then examined the role of AGR2 and TNF-α in regulating TJ proteins. Western blotting confirmed that TNF-α stimulation decreased the expression of ZO-1, claudin-1 and occludin (Fig. 4A–C) and that AGR2 plasmid transfection attenuated these decreases in expression (Fig. 4A–C). Immunofluorescence staining showed that in the control group, occludin and ZO-1 appeared as a continuous band surrounding the cell boundary, with no obvious gap. After 48 h of incubation with TNF-α, these proteins had rough edges and an interrupted distribution; there were visible irregular openings, with a honeycomb appearance between the cells of the monolayers. AGR2 plasmid transfection significantly reduced the TNF-α-induced damage to the TJs, causing the surfaces of the proteins to become completely adherent (Fig. 4D and E). These results indicated that AGR2 inhibited the TNF-α-induced decreases in expression of TJ proteins.

Figure 4

Western blot analysis showed that anterior gradient protein 2 homologue (AGR2) inhibited the decreased expression of tight junction (TJ) proteins (A) zonula occludens-1 (ZO-1), (B) claudin-1 and (C) occludin induced by TNF-α. The results are presented as the mean ± SD. **P<0.01 compared with controls; #P<0.05 compared with rhTNF-α-treated cells; ##P<0.01 compared with rhTNF-α-treated cells. Immunofluorescence staining shows that AGR2 inhibited the rhTNF-α-induced abnormal distribution of (D) occludin and (E) ZO-1 proteins.

AGR2 inhibits TNF-α-induced cytoskeletal F-actin rearrangement

Immunofluorescence staining showed that in the control group, F-actin was arranged in the cytoplasm in neat rows close to the cell membrane, forming a dense, smooth, continuous ring with a uniform distribution. After 48 h of incubation with TNF-α, cytoskeletal F-actin was rearranged, forming a fuzzy, peripheral actin ribbon with a decrease in the cortical F-actin fibre macula densa. Some cells had obvious transcellular stress fibre formation. AGR2 plasmid transfection inhibited the rearrangement of cytoskeletal F-actin, which appeared as a clear, peripheral actin ribbon with a decrease in cytoplasmic stress fibres (Fig. 5). The results indicated that AGR2 inhibited the TNF-α-induced rearrangement of cytoskeletal F-actin.

Figure 5

Immunofluorescence staining shows that anterior gradient protein 2 homologue (AGR2) inhibited the cytoskeletal F-actin rearrangement induced by TNF-α and stabilized the cytoskeletal structure.

AGR2 inhibits TNF-α activation of the MLCK/p-MLC pathway

The western blotting results showed that the expression of MLCK and p-MLC was significantly higher in cells incubated with TNF-α than levels noted in the control cells. Transfection with the AGR2 gene plasmid inhibited the TNF-α-induced elevations in MLCK and p-MLC expression (Fig. 6A and B). These results indicated that AGR2 attenuated the TNF-α-induced intestinal mucosal barrier injury by regulating the MLCK/p-MLC pathway.

Figure 6

Western blot analysis showed that anterior gradient protein 2 homologue (AGR2) inhibited the rhTNF-α-induced expression of (A) myosin light chain kinase (MLCK) and (B) p-MLC. The results are presented as the mean ± SD. **P<0.01 compared with the controls; #P<0.05 compared with the rhTNF-α group; ##P<0.01 compared with the TNF-α group.

AGR2 reduces TNF-α-induced barrier damage by inhibiting activation of NF-κB p65

Western blotting showed that TNF-α significantly increased nuclear NF-κB p65 protein expression and decreased cytoplasmic NF-κB p65 expression compared with that in the control group. In contrast, nuclear expression of this protein was decreased and cytoplasmic expression was increased in the Caco-2 cells transfected with the AGR2 plasmids (Fig. 7A and B). Immunofluorescence staining further confirmed the above results, showing that in the control group, the NF-κB p65 protein was mainly localized to the cytoplasm, where it was inactive. However, in the TNF-α-stimulated Caco-2 cells, this protein was predominantly nuclear. In the Caco-2 cells transfected with the AGR2 plasmids, nuclear accumulation of NF-κB p65 in response to TNF-α was significantly reduced (Fig. 7C). The results indicate that AGR2 may reduce intestinal barrier damage by inhibiting the activation of NF-κB p65.

Figure 7

Western blot analysis showed that anterior gradient protein 2 homologue (AGR2) inhibited the rhTNF-α-induced increase in (A) nuclear NF-κB p65 expression and decrease in (B) cytoplasmic NF-κB p65 expression. The results are presented as the mean ± SD. **P<0.01 compared with controls; ##P 0.01 compared with the rhTNF-α group. (C) Immunofluorescence staining showed that AGR2 inhibited the nuclear translocation of NF-κB p65 induced by rhTNF-α.

Discussion

The TJ complex is critical for maintaining mucosal barrier integrity after injury (30); however, the exact mechanism for primary repair of TJs has not been fully elucidated. The present study describes a novel mechanism by which AGR2 regulates TJ proteins and the cytoskeleton in response to TNF-α-induced intestinal barrier dysfunction. We report that TNF-α decreased AGR2 expression in the Caco-2 monolayers, while AGR2 overexpression inhibited the TNF-α-mediated intestinal barrier injury, reduced the permeability of Caco-2 monolayers, increased the expression of TJ proteins and stabilized the cytoskeletal structure by inhibiting NF-κB p65 mediated MLCK/p-MLC pathway activation.

Numerous previous studies, including those by our group, have confirmed that inflammatory cytokine-mediated intestinal epithelial barrier dysfunction contributes to multiple enteropathies, including IBD (31–34); such cytokines disrupt the integrity of the TJ complex and increase intestinal barrier permeability. A study by Chen et al showed that stimulating Caco-2 monolayers with 10 ng/ml TNF-α did not affect TJ protein expression levels but that TNF-α played a role in altering the distribution of TJ proteins (35). Other studies revealed that 10 ng/ml TNF-α led to both decrease expression and abnormal distribution of TJ proteins (36,37). In our study, stimulating Caco-2 monolayers with 100 ng/ml TNF-α significantly increased cell membrane permeability, accompanied by abnormal distribution and decreases in the expression of ZO-1, claudin-1 and occludin, as well as rearrangement of cytoskeletal F-actin; these findings are consistent with a study by Zhang et al (38). Our data further strengthens the evidence that TNF-α can disrupt the intestinal epithelial barrier by reducing TJ protein levels and reorganizing cytoskeletal structure.

More recently, it has been demonstrated that activation of the MLCK/p-MLC pathway plays a key role in inflammatory cytokine-mediated intestinal mucosal barrier dysfunction (39,40). To investigate the molecular mechanism by which TNF-α injures the intestinal barrier, we determined MLCK, MLC and p-MLC protein expression and found that TNF-α-induced barrier injury was accompanied by increases in both MLCK expression and MLC phosphorylation, which was also consistent with the findings of Cunningham et al (41).

Additionally, activation of NF-κB p65 also plays a crucial role in TNF-α-induced intestinal barrier injury. Previous research has shown that NF-κB binds to the promoter region of the MLCK gene and increases MLCK transcription and MLC phosphorylation, leading to the altered permeability and TJ disruption known to be associated with proinflammatory cytokines (42). Here, in our study, TNF-α significantly increased nuclear protein expression and distribution of NF-κB p65, indicating that NF-κB p65 is related to the intestinal barrier injury caused by TNF-α, consistent with the findings of Al-Sadi et al (43).

AGR2 is a recently discovered gene with a protective effect of mucosal barrier in IBD; however, the mechanism by which it regulates intestinal epithelial barrier function remains unclear. In the present study, we investigated the role of AGR2 in TNF-α-induced intestinal barrier injury and its related mechanisms. The results demonstrated that overexpression of AGR2 inhibited the TNF-α-induced decrease in TEER and increase in FD-40 flux, increased the expression and improved the distribution of TJ proteins, and stabilized the cytoskeletal structure, thereby ameliorating the TNF-α-induced cell membrane hyperpermeability. The impact of AGR2 on TNF-α-induced activation of the MLCK/p-MLC signaling pathway was then detected; AGR2 inhibited the changes in MLCK, MLC and p-MLC expression in response to TNF-α stimulation, preliminarily confirming that AGR2 improved intestinal barrier dysfunction through regulation of the MLCK/p-MLC pathway. Subsequently, we investigated whether activity of the transcription factor NF-κB p65 was also influenced by AGR2. The results revealed that AGR2 inhibited nulear protein expression of NF-κB p65, and immunofluorescence staining revealed that AGR2 inhibited NF-κB p65 translocation into the nucleus. Thus, these data suggest that inhibition of NF-κB p65-mediated MLCK/p-MLC pathway activation may be the molecular mechanism by which AGR2 ameliorates intestinal barrier dysfunction caused by TNF-α.

One limitation of the present study is that we tested the effect of AGR2 on NF-κB p65 and MLCK/p-MLC pathway expression in TNF-α-induced intestinal epithelial barrier dysfunction, but we did not specific block NF-κB p65 or MLCK gene expression. Further study is needed to investigate other potential mechanisms by which AGR2 ameliorates TNF-α-induced intestinal epithelial barrier injury.

In conclusion, to the best of our knowledge, this is the first study showing that the AGR2 gene inhibits TNF-α-induced intestinal epithelial hyperpermeability by enhancing TJ function and cytoskeletal stability. These effects may be exerted through the inhibition of NF-κB and MLCK/p-MLC pathway activation. In addition, this study may provide new evidence for treating IBD by upregulating AGR2 expression, and we hope that this study potentially helps improve the prognosis of IBD patients.