Recently the role of Parkinson’s disease 7 (PARK7) was studied in gastrointestinal diseases, however, the complex role of PARK7 in the intestinal inflammation is still not completely clear. Expression and localization of PARK7 were determined in the colon biopsies of children with inflammatory bowel disease (IBD), in the colon of dextran sodium sulphate (DSS) treated mice and in HT-29 colonic epithelial cells treated with interleukin (IL)-17, hydrogen peroxide (H2O2), tumor necrosis factor (TNF)-α, transforming growth factor (TGF)-β or lipopolysaccharide (LPS). Effect of PARK7 on the synthesis of IBD related cytokines was determined using PARK7 gene silenced HT-29 cells and 3,4,5-trimethoxy-N-(4-(8-methylimidazo(1,2-a)pyridine-2-yl)phenyl)benzamide (Comp23)—compound increasing PARK7 activity—treated mice with DSS-colitis. PARK7 expression was higher in the mucosa of children with Crohn’s disease compared to that of controls. While H2O2 and IL-17 treatment increased, LPS, TNF-α or TGF-β treatment decreased the PARK7 synthesis of HT-29 cells. PARK7 gene silencing influenced the synthesis of IL1B, IL6, TNFA and TGFB1 in vitro. Comp23 treatment attenuated the ex vivo permeability of colonic sacs, the clinical symptoms, and mucosal expression of Tgfb1, Il1b, Il6 and Il10 of DSS-treated mice. Our study revealed the role of PARK7 in the regulation of IBD-related inflammation in vitro and in vivo, suggesting its importance as a future therapeutic target.
IBD, including Crohn’s disease (CD) and ulcerative colitis (UC) is a chronic inflammatory disorder of the gastrointestinal tract that dramatically impacts the quality of life. IBD starting in childhood leads to a life-long disease, which is frequently accompanied by serious complications1,2,3. The incidence and prevalence of IBD are rapidly increasing and has become a major public health problem worldwide. Although the pathogenesis of IBD has not been fully elucidated the role of oxidative stress is indisputable. Indeed, chronic inflammation is accompanied by the continuous generation of reactive oxygen species (ROS), damaging the integrity of mucosal epithelial layer. Enhanced mucosal permeability promotes the invasion of immunogenic elements, including bacteria, which in turn further facilitate the local inflammation and ROS generation.
PARK7 is a small, ubiquitously expressed homodimer protein that was primarily studied regarding the central nervous system. Indeed, mutations of PARK7 have been proved to be associated with autosomal recessive early-onset Parkinson’s disease4, and its protective role was suggested in Alzheimer’s disease5 and stroke6, as well. Protective effect of PARK7 is related at least in part to its antioxidant effects. PARK7 quenches the effect of ROS through the oxidation of its cysteine residues, however more importantly it increases the expression of mitochondrial uncoupling proteins7, thus reducing the production of mitochondrial ROS. PARK7 also induces the synthesis of antioxidant enzymes superoxide dismutase 1 and 3, thus facilitating degradation of ROS8,9. Moreover, PARK7 was reported to stabilize nuclear factor erythroid-2-related factor 2 (Nrf2), the master transcription factor of oxidative stress10. However, accumulating studies reveal that besides its antioxidant effects, PARK7 has multiple functions: it has chaperone activity, it can inhibit the abnormal protein aggregation characteristic for neurodegenerative disorders and it has also been reported to be involved in ubiquitin–proteasome system6. In addition, recently anti-inflammatory effect of PARK7 was demonstrated via the inhibition of antigen-induced TNF-α and IL-4 production of mast cells11.
The above considerations, and also our previous studies demonstrating the role of PARK7 in the maintenance of small intestinal mucosal integrity12,13 led us to study the role of PARK7 in the pathogenesis of IBD. In this study we report the presence, regulation and role of PARK7 in the pathomechanism of mucosal inflammation using tissue samples of therapy-naive children with IBD, and in vitro and in vivo experimental models of colitis. Our study suggests the possible therapeutic relevance of PARK7 in the treatment of IBD.
Materials and methods
Children with newly diagnosed IBD (CD: n = 27 (15 for PCR, 19 for WB), UC: n = 18 (10 for PCR, 7 for WB)) and controls (n = 19 (10 for PCR, 10 for WB)) were enrolled in the present study (Table 1). IBD was diagnosed according to the “Porto criteria”14,15, and activity score was evaluated according to the Pediatric Crohn’s Disease or Ulcerative Colitis Activity Index (PCDAI or PUCAI)16,17. Colonic biopsy samples were taken from macroscopically inflamed (iCD) and non-inflamed (iCD) colonic mucosa regions of children with CD, and from inflamed colonic mucosa regions of children with UC. Controls were referred with chronic abdominal pain, diarrhoea or polyposis and their colonic biopsy showed normal macroscopic and histological appearance.
DSS-induced mouse model of colitis and Comp23 treatment
Experiments were performed on 7–8 weeks old, male C57Bl/6 J (WT; Charles River Laboratories, Sulzfeld, Germany) and Il17−/− mice18. Animals were housed in a temperature-controlled (22 ± 1 °C) room with alternating light and dark cycles and had free access to standard rat chow and water.
To investigate the effect of IL-17 on the synthesis of PARK7 wild type (WT) and Il17−/− mice were randomized into control groups receiving drinking water (0 day; n = 6/group) or DSS-treated groups gained drinking water containing 2.5% DSS (w/v; MP Biomedicals, LLC, Santa Ana, CA, USA) until the termination of the experiment on 3rd, 5th or 7th days (3, 5 or 7 days; n = 6/group). Colon samples were collected under general anesthesia induced by inhalation of isoflurane mixed with air using a vaporizer (Eickemeyer Veterinary Equipment Ltd., Twickenham, UK).
To investigate the effect of PARK7 on the pathomechanism of DSS-induced colitis, WT animals were treated with Comp23 (Enamine, Riga, Latvia), a PARK7-binding compound, that increase its activity by preventing the excessive oxidation of 106 cysteine residue of PARK7 protein, for 10 days19.
In this set of experiments mice were randomized into four groups receiving solvent (DMSO diluted with 20% physiology saline, i.p.; n = 6; Control group), Comp23 (10 mg/ttkg/die Comp23 dissolved in solvent, i.p.; n = 6; Comp23 group), DSS (as described above; n = 6; DSS group) or DSS and Comp23 (as described above; n = 6; DSS + Comp23 group). After the 7th day DSS was replaced by water in the DSS and DSS + Comp23 groups. Disease activity index (DAI) of animals were determined until the 10th day of the treatments. For molecular biological analyses the colon samples of another set of mice were collected on the 7th day of the experiment (Table 2).
Determination of weight loss and DAI
Changes in the body weight of mice were monitored during the whole experiment and measured on a digital scale in the same hour every day. DAI was determined as described in the literature previously20. Briefly, clinical signs of colitis including stool consistency and stool blood were scored from 0 to 3, and general state of animals was determined on a scale from 0 to 2 for 10 days. Total scores were calculated as the sum of values of the three categories. Body-weight loss and spleen weight of animals were also determined.
Ex vivo mucosal permeability measurement
Intestinal permeability was measured based on Mateer et al.21. Briefly, 2 cm long intestinal sacs were prepared from the colon of DMSO (Control) and Comp23 pretreated (10 mg/kg, intraperitoneally, 1 h before experiment) WT mice (n = 3–4/group). The intestinal sacs were equally filled with FITC-conjugated 4 kDa dextran (0.1 mg/ml; SigmaAldrich) and Rhodamine B-conjugated 70 kDa dextran (0.1 mg/ml; Sigma-Aldrich) diluted either in Dulbecco’s modified Eagle medium (DMEM; Thermo Fisher Scientific, Waltham, MA, USA) or in DMEM supplemented with H2O2 (1000 μM) and placed into 5 ml phosphate-buffered saline (PBS) at 37 °C. The permeation of dextrans was determined in every 20 min for 4 h. At the end of the experiment, the sacs were opened to determine the remnant dextran release (100%). Fluorescence intensities of PBS samples were measured at λexc: 485 nm, λem: 535 nm (Fluorescein) or λexc: 544 nm, λem: 632 nm (Rhodamine B) in a Hidex Chameleon Microplate Reader (Triathler, Plate Chameleon, 300SL Lablogic Systems, Inc., Brandon, FL, USA) using the MikroWin 2000 program.
Immunocytochemistry and immunofluorescence staining
HT-29 cells were seeded in chambers and cultured for 24 h at 37 °C. After repeated washing, cells were permeabilized with Cytofix/Cytoperm (BD Pharmingen, San Diego, CA, USA) for 15 min at room temperature (RT), and were washed again. Human frozen colon biopsy samples were embedded into Shandon cryomatrix (ThermoElectron Co., Madison, WI, USA) and cut into 5 μm sections. Thereafter cells or tissue sections were incubated with rabbit anti-human PARK7 or IL-17R polyclonal IgG primary antibody (Abcam, Cambridge, United Kingdom) (1:200) for 1 h at RT. Cells were washed with WashPerm solution, and tissue sections with PBS, thereafter incubated with Alexa Fluor 488 or 568 labelled chicken anti-rabbit IgG secondary antibody (1:200, Invitrogen, Life Technologies, Carlsbad, CA, USA) for 30 min at RT in the dark and then counterstained with Hoechst 33342 (1:2000, Sigma-Aldrich, USA) for 10 min. Finally, slides were coverslipped with Vectashield fluorescent mounting medium (Vector Laboratories, Burlingame, CA, USA). Appropriate controls were performed by omitting the primary antibodies to assure their specificity and to avoid autofluorescence. Fluorescence signals were analysed with a Nikon C2 confocal laser scanning microscope system (Nikon, Minato, Tokyo, Japan).
Paraffin sections of paraformaldehyde (4%, pH 7.4) fixed colon samples of mice were stained with hematoxylin–eosin or periodic acid–Schiff methods. Images were taken with Olympus IX81 microscope system (Olympus Corporation, Tokyo, Japan). Briefly, histological signs of colitis including (1) cell-rich subepithelial regenerative foci (granulation tissue), (2) mucosal infiltration of neutrophils, (3) oedema under the epithelial layer, (4) erosion and (5) vacuolation of epithelial cells were determined on a scale from 0 to 6, blindly by an expert pathologist. Histology score values were then calculated as the sum of scores of the above mentioned five categories.
HT-29 colonic epithelial cells and treatments
HT-29 human colonic epithelial cell line (Sigma-Aldrich) was cultured in modified McCoy’s 5A medium (Sigma-Aldrich) supplemented with l-glutamine, 10% heat-inactivated fetal bovine serum (FBS) (Invitrogen), 100 U/ml penicillin and 100 µg/ml streptomycin (Sigma-Aldrich) at 37 °C and 5% CO2.
Cells were starved in 0% FBS for 24 h then trypsinized and seeded in 6-well plates at a density of 5 × 105 cells/well, resulting in nearly 80% confluency. After plating, cells (n = 6/groups) were treated with 100 ng/ml recombinant human IL-17A (R&D Systems, Minneapolis, MN, USA), 20 µM H2O2 (Reanal, Budapest, Hungary), 10 ng/ml TNF-α (R&D Systems), 1 nM TGF-β (Life Technologies), or 100 ng/ml lipopolysaccharides (LPS) from Escherichia coli (Sigma-Aldrich) for 24 h at 37 °C. IL-17A, H2O2, TNF-α and LPS were dissolved in sterile PBS, TGF-ß was dissolved in 4 mM HCl. Control cells were treated only with vehicle.
To identify the IL-17-activated ROS-producing enzyme, cells were pretreated for 30 min with NAD(P)H-oxidase inhibitor, diphenyleneiodonium chlorid (DPI; 5 μM, Sigma-Aldrich) dissolved in DMSO.
PARK7 gene silencing and IL-17 treatment of HT-29 colonic epithelial cells
Exponentially growing cells were seeded in 6-well plates (5 × 105 cells/well, n = 6/group) and cultured for 24 h at 37 °C. Medium was replaced with Opti-MEM I reduced-serum medium (92.5 µl/ml, Invitrogen) containing 0% FBS, and PARK7 specific small interfering (si)RNA (30 nM, Invitrogen) and Lipofectamine RNAiMax Transfection Reagent (2.5 µl/ml, Invitrogen). Sense sequence of PARK7 siRNA was GGUUUUGGAAGUAAAGUUAtt. As negative control, cells were treated with the same medium containing Lipofectamine and a nonsense, short scrambled (sc)RNA (30 nM, Invitrogen), which is not complementary with any gene in the target organism. Cells were incubated in transfection reagent for 24 h. After transfection, cells were treated with vehicle or with recombinant human IL-17A (100 ng/ml) for 24 h.
RNA isolation and real-time RT-PCR
Total RNA was isolated from biopsy samples, mouse colon tissues or HT-29 colonic epithelial cells using Geneaid Total RNA Mini Kit (Geneaid Biotech Ltd., New Taipei City, Taiwan). RNA (1 μg/sample) was reverse-transcribed using Maxima First Strand cDNA Synthesis Kit for RT-qPCR (Life Technologies) to generate first-stranded cDNA. The mRNA expressions were determined by real-time RT-PCR using a Light Cycler 480 system (Roche Diagnostics, Mannheim, Germany). Nucleotide sequences, annealing temperatures of the primer pairs and resulted PCR product lengths are shown in Table 3.
The expected lenght of the PCR products were monitored by gele electrophoresis (2% agarose gel, Bioline, London, UK). The melting curves and the relative mRNA expressions were analysed by a Light-Cycler 480 software, version 220.127.116.11 (Roche) and determined by comparison with GAPDH, RPLP0 or 18S as internal control using the ΔΔCt method. Data were normalized and presented as the ratio of their control values.
Protein isolation and western blotting
Colonic tissue samples from patients, mice or HT-29 colonic epithelial cells were homogenized in lysing solution, containing 50 mM HEPES, 150 mM NaCl, 1% Triton X-100, 5 mM EDTA, 5 mM EGTA, 20 mM sodium pyrophosphate, 20 mM NaF, 0.2 mg/ml phenylmethylsulfonyl fluoride, 0.01 mg/ml leupeptin, and 0.01 mg/ml aprotinin (pH 7.4) (each substance obtained from Sigma-Aldrich). Thereafter protein concentration was determined by a detergent-compatible protein assay (BioRad, Hercules, CA, USA). Denatured samples (20 μg protein/lane) were separated on 4–20% gradient SDS polyacrylamide gel (BioRad) and transferred to nitrocellulose membranes (BioRad). Pre-stained protein standard (BioRad) was used as molecular weight marker. Blot membranes were then cut in two pieces to determine the amount of PARK7 and that of the corresponding loading control from identical samples. Membranes were blocked in 1% non-fat dry milk solution for 1 h and incubated with PARK7-specific rabbit polyclonal antibody (1:300) overnight (Abcam). Equal protein loading was confirmed by β-actin specific rabbit polyclonal IgG antibody (1:2000, Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA), GAPDH specific rabbit polyclonal IgG antibody (1:2000, Santa Cruz Biotechnology Inc.), or total protein amount. Then blots were incubated with horse radish peroxidase (HRP)-conjugated goat anti-rabbit IgG secondary antibody (1:2000, Santa Cruz Biotechnology Inc.) for 30 min. Immunoreactive bands were developed using the enhanced chemiluminescence Western blotting detection protocol (GE Healthcare, Little Chalfont, United Kingdom) and the resulted images were visualized with VersaDoc 5000MP system (Bio-Rad) and analyzed using Quantity One v4.6.9 (Bio-Rad) and ImageJ 1.48v (National Institutes of Health, Bethesda, MD, USA) softwares, the results were expressed as relative optical density.
Enzyme-linked immunosorbent assay (ELISA)
Protein level of TNF-α in the lysate of PARK7 gene silenced HT-29 colonic epithelial cells was measured using human TNF-α DuoSet ELISA (R&D Systems) according to the manufacturer’s protocol. Absorbance was recorded at 450 nm and at 570 nm as background using a Hidex Chameleon Microplate Reader (Triathler, Plate Chameleion, 300SL Lablogic Systems, Inc., Brandon, FL, USA) and MikroWin 2000 software.
HT-29 cells were centrifuged, washed with PBS and incubated for 10 min at RT with FACS Permeabilizing Solution 2 (BD Pharmingen). Permeabilized cells were washed with PBS and incubated with rabbit anti-human PARK7 polyclonal IgG primary antibody (1:25, AbCam) for 30 min at RT. Cells were subsequently washed with Permeabilizing Solution 2 and incubated with Alexa Fluor 488 chicken anti-rabbit IgG secondary antibody (1:50, Invitrogen) for 30 min at RT in dark. Negative controls were incubated with the secondary antibody alone. Thereafter cells were washed with Permeabilizing Solution 2, centrifuged and resuspended in PBS. Analysis was performed with BD FACSAria cytometer (BD Pharmingen). We identified an intact cell gate, according to the forward and side scatter. 104 cells were collected and results were analysed using BD FACSDiva Software (BD Pharmingen).
Data were analyzed using GraphPad Prism 5.0. software (GraphPad Software Inc., La Jolla, CA, USA). After testing the normality with Kolmogorov–Smirnov test, ordinary one- or two-way ANOVA- and unpaired- or multiple t-test, Mann–Whitney or Kruskall–Wallis-test were used to determine the differences among groups. Results were illustrated as mean + SEM with dots, representing individual values. P values less than 0.05 were considered to statistically significant.
Written informed consent was obtained from parents of each participant prior to the procedure. Study was approved by the Semmelweis University Regional and Institutional Committee of Science and Research Ethics (TUKEB 58/2013) and performed in compliance with the Declaration of Helsinki.
All animal procedures were approved by the Committee on the Care and Use of Laboratory Animals of the Council on Animal Care at Semmelweis University, Budapest, Hungary (PEI/001/82-4/2013). All methods were carried out in accordance with the relevant regulations and ARRIVE guidelines.
Presence of PARK7 in the colonic mucosa of children
The mRNA expression (Fig. 1a) and protein amount (Fig. 1b,c) of PARK7 were increased in the macroscopically inflamed (iCD) and non-inflamed (niCD) colonic mucosa of children with CD compared to controls. Amount of PARK7 remained unchanged in the colonic mucosa of UC patients. Strong PARK7 immunopositivity was observed in epithelial and lamina propria cells of children with CD (Fig. 1d–g).
Effect of IL-17, H2O2, TNF-α, TGF-β, LPS, and DPI treatment on PARK7 synthesis of HT-29 cells
HT-29 cells showed IL-17R immunopositivity (Fig. 2a). While IL-17 or H2O2 treatment increased, TNF-α, TGF-β or LPS treatment decreased the amount of PARK7 (Fig. 2c,d,f,g). The increased PARK7 expression of IL-17 treated cells was inhibited by pretreatment with DPI, a NAD(P)H oxidase inhibitor (Fig. 2e).
Effect of DSS treatment on the colonic Il17, Tnfα and PARK7 synthesis of WT and Il17−/− mice
mRNA expression of Il17 was increased on the 5th day in the colon of DSS-treated WT mice (Fig. 3a). While mRNA expression of Tnfα was increased only on the 7th day in the colon of WT mice, it was increased on the 3rd day and remained elevated until the end of experiment in the colon of DSS-treated Il17−/− mice compared to the corresponding controls (Fig. 3b).
While mRNA expression of Park7 was increased on the 3rd day and protein level on the 3rd and 5th day in the colon of DSS-treated WT mice, it remained unchanged in the Il17−/− mice (Fig. 3c–e).
Effect of PARK7 gene silencing on TNFA, IL1B, IL6, IL10 and TGFB1 expression
Treatment with PARK7-specific siRNA resulted in decreased mRNA expression and protein level of PARK7 both in untreated and IL-17 treated HT-29 cells (Fig. 4a,c,f,g).
PARK7 gene silencing increased mRNA expression of TNFA, TGFB1 and decreased that of IL1B and IL6 as compared to control cells (Fig. 4b).
IL-17 treatment increased mRNA expression and protein level of PARK7, and mRNA expression of TNFA, IL1B, IL6; however, decreased mRNA expression of TGFB1 of HT-29 cells as compared to controls (Fig. 4d).
PARK7 gene silencing further increased mRNA expression and protein level of TNF-α of IL-17 treated HT-29 cells as compared to control or IL-17 treated cells (Fig. 4d,e). Neither IL-17 treatment, nor PARK7 gene silencing had any effect on the mRNA expression of IL10 in colonic epithelial cells (Fig. 4b,d).
Effect of PARK7-binding Comp23 on DSS induced colitis of mice
Intraperitoneal administration of Comp23 reduced body-weight loss (Fig. 5a) and spleen enlargement (Fig. 5c) and improved DAI (Fig. 5b) of DSS compared to vehicle-treated mice. In accordance with the clinical picture Comp23 treatment also reduced histological lesions in the colon of the DSS-treated mice (Fig. 5d,e). Indeed, Comp23 treatment reduced subepithelial immune cell infiltration and mucosal damage, hereby preserved the appearance of crypts and microvilli of DSS-treated mice (Fig. 5e).
Comp23 treatment increased the amount of PARK7 in the colon of DSS-treated mice compared to that of control, Comp23 or DSS-treated mice (Fig. 5k,l).
Effect of PARK7-binding Comp23 on the intestinal permeability of mice
The H2O2 induced permeability of colon sacs, derived from Comp23 treated mice, to 4 kDa (Fig. 6a) and 70 kDa (Fig. 6b) dextrans was less than that of the sacs derived from vehiculum treated control mice.
Previously, involvement of PARK7 was described in disorders affecting the central nervous system, including Parkinson’s4 or Alzheimer’s disease22. However, there are a few studies investigating the role of PARK7 in gastrointestinal diseases. Indeed, recently our research group demonstrated the role of PARK7 in the maintenance of duodenal mucosal integrity of children with coeliac disease12,13, and Di Narzo23 and Zhang et al.24 investigated the amount of PARK7 in the plasma and intestine of adult patients with IBD, respectively. PARK7 was also shown to play a role in the pathomechanism of premature piglet model of enteral feeding induced necrotizing enterocolitis25, and in ketoprofen-induced oxidative damage of intestinal mucosa26.
In the present study, we demonstrated increased amount of PARK7 in the epithelial and lamina propria cells of macroscopically inflamed and non-inflamed mucosa of therapy-naive paediatric patients with CD compared to that of controls (Fig. 1). Interestingly, mucosal PARK7 level of children with UC remained at the level of controls. Our results are differing from that of Di Narzo23 who found higher PARK7 level in the plasma of UC compared to CD patients or that of Zhang et al.24, demonstrating decreased amount of PARK7 in intestinal samples of patients with IBD. However, these studies are hardly comparable with our one, because of the different type of samples, patients or methods. Indeed, Di Narzo investigated the plasma proteome of adult IBD patients, who were being treated, using a SOMAmer-based high throughput capture array23. Less is known about the biopsy specimens and their parameters used by Zhang et al., who investigated the PARK7 immunopositivity of paraffin-embedded colon sections of IBD patients24.
Nevertheless, our present study demonstrates significant difference between mucosal PARK7 level of children with CD and UC. Although our observation needs further, large scale confirmation, we hope that determination of mucosal amount of PARK7 may contribute to the easier differential diagnosis of CD and UC in the future, especially in children with. The importance of our finding is particularly highlighted by the fact that the accurate diagnosis of the indeterminate forms of IBD often takes years27,28. One can hypothesize, that the observed difference may be due to the well-known immunological differences between the different forms of IBD. Indeed, while CD is characterized by transmural inflammation and the activation of Th1 and Th17 cells29,30, UC is characterized by Th2/NKT cell dominance and inflammation affecting the mucosal surface31,32.
To explore the underlying mechanisms responsible for the regulation of PARK7 synthesis more deeply, we investigated the effect of different IBD-related factors, including IL-17, TNF-α, TGF-β, H2O2 or LPS on PARK7 expression by HT-29 colonic epithelial cells (Fig. 2). In these experiments we demonstrated that all investigated factors influenced the synthesis of PARK7. However, we found that while IL-17 or H2O2 treatment increased, TNF-α, TGF-β or LPS treatment decreased the PARK7 expression by HT-29 cells.
To the best of our knowledge, present study is the first demonstrating the role of IL-17 in the regulation of PARK7 synthesis. IL-17 is the main secreted cytokine of the Th17 cells and plays a central role in the pathomechanism of IBD. Indeed, previous studies demonstrated the increased expression of IL-17 in the inflamed mucosa and sera of patients with IBD33,34,35. Moreover, the expression of mucosal IL-17 correlates with disease activity index, endoscopic and histological scores of active IBD patients36. Therefore, further investigating the effect of IL-17 on the PARK7 synthesis we found that while it increased in the colon of DSS treated WT mice, it remained unchanged in the colon of Il17−/− mice with DSS induced colitis (Fig. 3c–e). It should be noted that according to the literature, similarly to the observed alteration of mucosal PARK7, the number of Th17 cells and also the expression of IL-17 is elevated in the mucosa of CD patients compared to that of UC patients, suggesting the possible role of IL-17 in the regulation of PARK7 synthesis in vivo33,35.
It was shown that IL-17 induces the production of ROS through the activation of NADPH–oxidase37 and also that ROS is a potent inducer of PARK7 synthesis38,39,40. In accordance with these literary data, we found that administration of DPI, an inhibitor of NADPH oxidases, inhibits the IL-17 induced synthesis of PARK7 by HT-29 cells (Fig. 2e), underlying the relevance of ROS in the regulation of PARK7 synthesis.
In our further experiments, we demonstrated that TGF-β treatment resulted in decreased synthesis of PARK7 by HT-29 colon epithelial cells (Fig. 2c,f). Previously, Del Zotto B. et al. found increased TGF-β production in the lamina propria mononuclear cells of UC patients compared to CD patients or controls41. Therefore, it is conceivable that increased mucosal production of TGF-β in UC patients may contribute to the decreased presence of PARK7 in their colonic tissue observed in our study.
Finally, environmental factors, including infections are thought to alter the barrier function of intestinal mucosa, thus promoting the development of IBD42,43,44. Bacterial LPS is recognized by innate immune system via Toll-like receptor 4 (TLR4), leading to increased secretion of immunoregulatory molecules, including TNF-α45,46. In the present study, we demonstrated that both LPS and TNF-α treatment decreased the PARK7 synthesis of HT-29 cells (Fig. 2c,d,f,g). These results are in accordance with that of Khasnavis et al., who have found that LPS treatment inhibits the expression of PARK7 in primary human neurons and astrocytes47.
Taken together all the above mentioned differences regarding the intestinal inflammation of patients with CD or UC may explain at least in part the observed difference in their mucosal amount of PARK7.
In the next set of experiments, we investigated the biological role of PARK7 in mucosal inflammation. First, we examined the effect of PARK7 on the synthesis of IBD-related inflammatory cytokines of intestinal epithelial cells in vitro. We found that gene silencing of PARK7 significantly alters the expression of many inflammation-related factors (Fig. 4). Indeed, we found that expression of TNF-α increased in PARK7 gene silenced HT-29 cells (Fig. 4b). Interestingly, the expression of TNF-α was even higher in the PARK7 knockdown HT-29 cells treated with IL-17 compared to IL-17 treated or control HT-29 cells (Fig. 4d,e). Similarly, increased expression of TNFA was observed in DSS-treated IL17−/− mice (Fig. 3b)—in which the expression of PARK7 remained unchanged (Fig. 3c–e)—compared to WT mice, suggesting that PARK7 plays a determinative role in regulation of TNF-α in vitro and , in vivo as well. There are only few literary data regarding role of PARK7 in the regulation of inflammatory factors. However, similarly to our results Kim et al. described that antigen-induced TNF-α synthesis is higher in mast cells isolated from Park7−/− mice as compared to those isolated from WT48.
Our data also demonstrated increased TGFB expression in PARK7 gene silenced cells, which is in line with the results of Gao et al. who found that PARK7 suppresses TGF-β/Smad pathway, and partially restores pulmonary arterial hypertension of rats49.
Moreover, we found that in the absence of PARK7, the expression of other inflammatory cytokines, including IL1B and IL6 was decreased (Fig. 4b). Further investigating the effect of PARK7 gene silencing, we also examined its effect on IL1 and IL6 expression in IL-17 treated HT-29 colon epithelial cells. Indeed, we found that similarly to our previous experiment, PARK7 gene silencing decreased IL1B expression of IL-17 treated, but it had no effect on IL6 expression (Fig. 4d). One reason of this latter discrepancy can be that while IL-17 treatment had only a little effect on the IL1B expression, it increased significantly by about fivefold the expression of IL6, which may have suppressed the effect of PARK7 gene silencing. We must also note that in contrast with our results Chien CH et al. observed elevated IL-1β level in lung of Park7−/− mice and in Park7 knockdown macrophages, as well50.
Taken together our data demonstrate, that PARK7 synthesis is regulated by a number of factors playing a central role in the pathomechanism of IBD, and conversely PARK7 itself can influence the synthesis of several IBD related inflammatory factors.
Based on these data it is easy to accept that PARK7 is an important player in the pathomechanism of IBD. Therefore, in the following experiment, we examined the biological effects of the recently developed PARK7 binding Comp23 on DSS-induced mouse model of IBD19. The PARK7 specific effect of Comp23 was evidenced in Park7−/− cells and mice where the protective, antioxidant effects of the compound were ceased19,51. Indeed, Comp23 is thought to prevent the excessive oxidation of 106 cysteine residue of PARK7, thus retaining its activity51.
In our in vivo experiments, Comp23 treatment significantly improved clinical symptoms of DSS induced colitis, it reduced body-weight loss and improved DAI values, as well (Fig. 5a,b). Our results are in line with observation of Zhang et al. who observed worse clinical symptoms in DSS-treated Park7−/− than in DSS treated WT mice24. Moreover, in accordance with the clinical symptoms, Comp23 treatment reduced enlargement of spleen, preserved normal appearance of crypts and microvilli and decreased the number of immune cells in colonic subepithelial layer of DSS-treated mice (Fig. 5c–e). To further investigate the significance of PARK7 in the mucosal pathology, we examined the effect of Comp23 on the H2O2-treatment induced permeability of ex vivo colon preparations (Fig. 6). In line with our previous experiments on small intestinal sacs13, we found that Comp23 greatly decreased the permeability of H2O2-treated colon sacs (Fig. 6), confirming the determinative role of PARK7 in the maintenance of mucosal integrity.
Investigating the molecular biological processes underlying the better clinical symptoms, we found that Comp23 treatment significantly increased the amount of PARK7 in the colon of DSS-treated mice (Fig. 5k,l). Perhaps it is not so surprising, since previously it has been demonstrated that Comp23 prevents the excessive oxidation of 106 cysteine residue of PARK7, which thus in line with the study of Takahashi-Niki K et al. may inhibit the oxidation induced chaperone-mediated degradation of PARK751.
We also found that Comp23 treatment resulted in decreased expression of Il1b, Il6 and Tgfb1 in colonic mucosa of DSS-treated mice (Fig. 5g–i). These cytokines are determinatives in the maturation of Th152, Th17 and Treg53 cells, which are responsible for the mucosal inflammation in CD54.
However, interestingly Comp23 treatment also decreased expression of Il10 a potent anti-inflammatory cytokine (Fig. 5j). Considering that in our experiments Park7 gene silencing did not alter expression of Il10 (Fig. 4b), we suggest that decreased colonic expression of Il10 may be rather an indirect consequence of decreased inflammation, observed in Comp23 treated mice with DSS induced colitis.
Finally, we must also note that our results of Comp23 treated mice with DSS-induced colitis are not completely consistent with our in vitro experiments. Although, the observed difference in the expression of IL1 and IL6 may be simply due to differences in the complexity of an in vitro and in vivo model, we believe that the main point is different. Indeed, while in our in vitro experiments gene silencing decreased the amount of PARK7 in case of our in vivo experiment Comp23 treatment increased its amount. Moreover, Comp23 treatment by protecting PARK7 from its oxidation may also increase its activity.
In summary, although there are limitations of our study, including the number of the human samples, which do not let us to correlate the mucosal amount of PARK7 with disease activity index or other clinical parameters, we made great progress in the understanding of the biological effects of PARK7 in the pathomechanism of IBD. Indeed, we showed that PARK7 is differentially expressed in the mucosa of children with CD or UC, suggesting that quantifying the expression of PARK7 may help to differentiate between the two main clinical forms of IBD. Moreover, our in vitro experiments demonstrated that IBD related factors influence the synthesis of PARK7, suggesting that their local balance may be responsible for the observed differences in mucosal PARK7 level of children with CD and UC, as well. We also showed that presence of PARK7 alters the expression of many IBD-related factors in vitro. Finally, in the present study we demonstrated for the first time that PARK7 binding Comp23 treatment reduces mucosal inflammation and clinical symptoms of DSS-induced colitis, suggesting its possible therapeutic value. Taken together, our present work contributes to better understanding the role of PARK7 in mucosal inflammation and may facilitate the development of new therapeutics to hinder IBD.
The data used to support the findings of this study are included within the article.
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We dedicate this manuscript to the memory of our dear friend and colleague Gábor Veres. We are grateful to András Arató for his helpful advice in clinical issues and to Mária Bernáth for her excellent technical assistance.
This paper was supported by János Bolyai Research Scholarship of Hungarian Academy of Sciences, OTKA K116928, K125470, 20382-3/2018 FEKUTSTRAT Grants, Semmelweis Science and Innovation Fund, STIA-KFI-2020.
The authors declare no competing interests.
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Lippai, R., Veres-Székely, A., Sziksz, E. et al. Immunomodulatory role of Parkinson’s disease 7 in inflammatory bowel disease. Sci Rep 11, 14582 (2021). https://doi.org/10.1038/s41598-021-93671-1