Objective Proline–glycine–proline (PGP) has been shown to have chemotactic effects on neutrophils via CXCR2 in several lung diseases. PGP is derived from collagen by the combined action of matrix metalloproteinase (MMP) 8 and/or MMP9 and prolyl endopeptidase (PE). We investigated the role of PGP in inflammatory bowel disease (IBD).
Design In intestinal tissue from patients with IBD and mice with dextran sodium sulfate (DSS)-induced colitis, MMP8, MMP9 and PE were evaluated by ELISA, immunoblot and immunohistochemistry. Peripheral blood polymorphonuclear cell (PMN) supernatants were also analysed accordingly and incubated with collagen to assess PGP generation ex vivo. PGP levels were measured by mass spectrometry, and PGP neutralisation was achieved with a PGP antagonist and PGP antibodies.
Results In the intestine of patients with IBD, MMP8 and MMP9 levels were elevated, while PE was expressed at similar levels to control tissue. PGP levels were increased in intestinal tissue of patients with IBD. Similar results were obtained in intestine from DSS-treated mice. PMN supernatants from patients with IBD were far more capable of generating PGP from collagen ex vivo than healthy controls. Furthermore, PGP neutralisation during DSS-induced colitis led to a significant reduction in neutrophil infiltration in the intestine.
Conclusions The proteolytic cascade that generates PGP from collagen, as well as the tripeptide itself, is present in the intestine of patients with IBD and mice with DSS-induced colitis. PGP neutralisation in DSS-treated mice showed the importance of PGP-guided neutrophilic infiltration in the intestine and indicates a vicious circle in neutrophilic inflammation in IBD.
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Significance of this study
What is already known on this subject?
Proline–glycine–proline (PGP) is a collagen-degradation product that mediates neutrophil infiltration into the lung via CXCR2 in inflammatory lung diseases such as chronic obstructive pulmonary disease and asthma.
PGP is formed from collagen by the combined action of matrix metalloproteinase (MMP) 8/9 and prolyl endopeptidase (PE).
Both collagen proteolysis and neutrophil infiltration are extensively present in inflammatory bowel disease (IBD).
What are the new findings?
The PGP generation cascade (MMP8/9 and PE) and PGP itself are present in the intestines of patients with IBD and mice with dextran sodium sulfate (DSS)-induced colitis.
PGP neutralisation reduced neutrophilic infiltration in the intestine of DSS-treated mice.
How might it impact on clinical practice in the foreseeable future?
Our results show that reducing collagen degradation in the intestine of patients with IBD not only reduces intestinal damage, but also reduces neutrophilic infiltration into the intestine, which opens up new avenues for treating the chronic inflammation found in IBD.
Neutrophils are key inflammatory cells in the innate defence against invading pathogens. The recruitment of neutrophils to the site of inflammation is controlled and directed by the release of endogenous and/or pathogen-derived chemoattractant signals.1 Classic endogenous chemoattractants for neutrophils are CXC chemokines such as CXCL8, CXCL1, CXCL2 and CXCL3 in humans and CXCL1 and CXCL2 in mice.2 These chemokines induce migration and activation by binding to specific G-protein-coupled receptors on the surface of neutrophils, mainly CXCR1 and CXCR2 in humans and CXCR2 in mice.3
Fragments of the extracellular matrix, such as collagen fragments, can also have chemotactic properties.4 Recently, a collagen-derived fragment, proline–glycine–proline (PGP), was shown to have chemotactic effects on neutrophils via CXCR2.5 The tripeptide, PGP, is formed from collagen by the combinational action of matrix metalloproteinases (MMPs) and prolyl endopeptidase (or prolyl oligopeptidase) (PE).6 MMP8 and/or MMP9 are responsible for cleavage of collagen into smaller (<30 kDa) fragments, which allow further cleavage by PE. Acetylation of PGP leads to N-acetyl N-Ac-PGP, which is a more potent chemoattractant for neutrophils than PGP itself.7 The formation of PGP (and N-Ac-PGP) and subsequent neutrophilic infiltration plays an important role in, and is a potential biomarker for, chronic obstructive pulmonary disease and other lung diseases, such as cystic fibrosis.5 ,8 ,9
In inflammatory bowel diseases (IBDs), with the clinical manifestations Crohn's disease (CD) and ulcerative colitis (UC), luminal disease activity is accompanied by extensive neutrophilic inflammation.10 In addition to the role of chemokines and their receptors in IBD,11 ,12 collagen remodelling and the role of MMPs have also been extensively studied in this disease.13 Most of these MMPs show enhanced expression and/or activity in the bowel of patients with IBD. PE is found in all tissues including the intestine.14 Similarly, in vivo models of colitis, such as the dextran sodium sulfate (DSS) model, are dependent on proteolytic enzymes.15 ,16 Moreover, blocking CXCR2 with antibodies or CXCR2 antagonists reduces DSS-induced colitis,17 and CXCR2 knock-out animals are resistant to DSS-induced colitis.18
The aim of the present study was to investigate the components of the collagen-degradation pathway that lead to the production of PGP (MMP8, MMP9 and PE) in IBD. To determine the role of PGP in neutrophilic migration in intestinal inflammation, we investigated these components and the effects of PGP neutralisation in mice with DSS-induced colitis. We hypothesised that, in the bowel of patients with IBD and in mice with DSS-induced colitis, collagen breakdown leads to the production of PGP, enhancing neutrophil chemotaxis to the intestine and exaggerating the disease.
Materials and methods
Macroscopically inflamed/affected as well as non-inflamed/unaffected intestinal mucosa from patients with IBD and colorectal cancer controls was prospectively collected after surgical resection at the Leiden University Medical Centre, The Netherlands. The procedure for homogenising intestinal tissue and methods of assaying myeloperoxidase (MPO) activity and MMP9 protein levels have been reported previously.19 The characteristics, MPO activities and MMP9 levels of the subpopulation of patients used here are presented in online supplementary figure S1(A–C). The patients in the polymorphonuclear cell (PMN) study (online supplementary figure S1D) were recruited at the Department of Gastroenterology in the Academic Medical Centre, Amsterdam, The Netherlands. For all studies with human samples, protocols were executed according to the guidelines of the local medical ethics committee and in compliance with the Helsinki Declaration.
Preparation of human samples for PGP measurement
Intestinal tissue homogenates (n=60) of the same patient resection material were made. Tissue was weighed and homogenised in 1 mM bestatin/phosphate-buffered saline (PBS) (100 mg tissue/ml) using a Precellys 24 tissue homogeniser (Bertin Technologies, France) five times for 10 s at 6000 rpm with a minimum 5 min cooling period on ice in between. Samples were then centrifuged for 15 min at 14 000 rpm, and the supernatant was transferred to a clean tube.
PMN studies and ex vivo PGP generation
PMNs were isolated from fresh peripheral blood from patients with IBD and healthy controls as previously described,20 and incubated (105 cells/well) in 100 μl RPMI medium 1640 (Lonza Verviers SPRL, Verviers, Belgium) for 6 h. PMNs from healthy controls were also incubated with 10 ng/ml lipopolysaccharide (LPS) (Sigma-Aldrich Chemie, Zwijndrecht, The Netherlands) for 6 h. A 90 µl sample of this PMN-conditioned medium (105 cells/100 μl/well) was incubated with 10 µl of a 1 mg/ml solution of type I collagen (Sigma-Aldrich) in PBS for 24 h at 37°C and 5% CO2 to assess collagen breakdown to (N-Ac-)PGP ex vivo. The collagen was extensively dialysed beforehand to remove PGP.
Measurement of PGP and N-Ac-PGP
Before peptide measurement, samples were 10 kDa-filtered (Millipore). PGP and N-Ac-PGP levels in mouse samples and the ex vivo PGP generation assay were analysed as described previously.5 Human intestinal samples were analysed using a Finnigan TSQ Quantum Discovery Max quadrupole mass spectrometer with electrospray ionisation (Thermo Fisher Scientific, San Jose, California, USA) on an Atlantis dC18 column (100 mm×2.1 mm, dp=3 μm; Waters Chromatography, Milford, Massachusetts, USA) with an Atlantis dC18 pre-column (10 mm×2.1 mm, dp=3 μm; Waters). Positive electrospray mass transitions were monitored at 270>70, 270>116 and 270>173 for PGP and 312>140, 312>112 and 312>70 for N-Ac-PGP.
Human (hu)CXCR2 C57Bl6 knock-in animals were bred under standard housing conditions with drinking water and food available ad libitum, and genotyped as described previously.21 Colitis was induced in male huCXCR2 knock-in mice (8–12 weeks old) by administration of 1.5% (w/v) DSS (MP Biomedicals, Aurora, Ohio, USA; molecular mass=36 000–50 000 Da) in tap water to the mice for 5 consecutive days. After a 10-day tap water recovery phase, a second 5-day DSS period was instituted. Mice were killed by CO2 suffocation. All animal studies were approved by the ethics committee for animal studies of Utrecht University.
PGP neutralisation protocols
The neutralising PGP antagonist, arginine–threonine–arginine (RTR; 300 μg/100 μl PBS; Anaspec, San Jose, California, USA), and polyclonal PGP antibody (30 μg/100 μl PBS; EZBiolabs, Westfield, Indiana, USA) were administered by intravenous injection into the tail vein, every day from day 0 to day 6. Control mice were intravenously injected daily with 100 μl PBS or 30 μg/100 μl isotype control (rabbit IgG; R&D Systems, Minneapolis, Minnesota, USA).
Assessment of colitis
The presence of blood in faeces (0=none, 1=positive, 2=visible), stool consistency (0=normal, 1=loose stools, 2=diarrhoea) and general appearance (0=normal, 1=hunched back, 2=lethargic) were recorded daily for each animal. Together, these factors constitute the Disease Activity Index (DAI, range 0–6), as described previously.22
Histopathology and intestinal tissue sampling
The large intestines of the killed mice were isolated, and the length was measured in a relaxed position without stretching. The large intestine was opened longitudinally, cleaned in PBS, and longitudinally divided into two pieces. One part was embedded in paraffin (Swiss-role technique), and the other part was stored at −80°C until homogenisation in 1 ml ice-cold PBS as described previously.23 Protein concentration was determined using the BCA protein assay kit (Thermo Fisher Scientific). Histology of standard H&E slides was scored in a blinded fashion by scoring crypt loss and influx of inflammatory cells with a number from 0 (normal) to 4 (severe), and for the amount of affected colon (1, <25%; 2, 25–50%; 3, 50–75%; 4, 75–100%). The sum of these scores is the histological score (0–16).
Immunohistochemistry was performed as described previously.22 Antigen retrieval was carried out by boiling the slides in 10 mM citrate buffer (pH 6.0) for 10 min in a microwave oven. The slides were blocked with 5% goat serum (Dakocytomation, Glostrup, Denmark) in 1% BSA in PBS for 20 min at room temperature. The sections were then incubated with primary antibodies (rabbit anti-MMP8 (1:400 dilution; Lifespan Biosciences; LS-C48493), rabbit anti-MMP924 (1:400 dilution), rabbit anti-PE (1:500 dilution; ProteinTech Group, USA) or rat anti-mouse Ly-6B.2 (1:400 dilution; AbD Serotec, UK; MCA771GA)) in 1% BSA/PBS overnight at 4°C. Detection was carried out with biotinylated goat anti-rabbit secondary antibodies (1:200 dilution; Dakocytomation), streptavidin–avidin–biotin complex/horseradish peroxidase (HRP) (Vectastain Elite ABC; Vector Laboratories) and diaminobenzidine tetrahydrochloride (Sigma-Aldrich). Sections were counterstained with Mayer’s haematoxylin (Merck), dehydrated and mounted. Slides that had not been incubated with primary antibody were included as negative controls. Photomicrographs were taken with an Olympus BX50 microscope equipped with a Leica DFC 320 digital camera.
Quantification of CXCL1, CXCL2, MMP8, MMP9, leukotriene B4 (LTB4) and MPO
MMP8 (human: R&D systems; mouse: Cusabio Biotech), LTB4 (R&D systems) and total and pro-MMP9 (both R&D Systems) concentrations and MPO activity (Mouse MPO ELISA Kit; Hycult Biotechnology, Uden, The Netherlands) were determined using ELISA kits. The concentration of active MMP9 was calculated by subtracting pro-MMP9 from total MMP9. The levels of CXCL1 and CXCL2 were measured using a mouse multiplex assay according to the manufacturer's instructions (Millipore Corporation, Billericia, Massachusetts, USA). MMP8 and MMP9 levels in PMN-conditioned medium were quantified using a Fluorokine MAP Human Base Kit (R&D Systems).
The presence of active and latent forms of MMP9 was analysed by zymography on 11% polyacrylamide gel containing 1% porcine skin gelatin (Sigma-Aldrich) as previously described.24
Assay of PE activity
PE activity was measured using the fluorogenic substrate, Z-Gly-Pro-7-amido-4-methylcoumarin (Z-GP-AMC; Bachem, Budendorf, Germany), as described previously.25 Tissue homogenate (20 µl; 5 μg) or PMN-conditioned medium (20 µl) was incubated with 80 µl assay buffer (100 µM Z-GP-AMC in 25 mM Tris/HCl, 0.25 M NaCl, pH 7.5, 2 mM DTT) at 37°C. The fluorescence from released AMC was monitored using a Fluostar reader at an excitation wavelength of 355 nm and an emission wavelength of 460 nm. Fluorimetric intensities observed were converted into pmol AMC released per minute using appropriate AMC standard curves. PE activity was expressed as pmol AMC/min or pmol AMC/min/mg protein.
Homogenates were separated on 10% (w/v) SDS gels and blotted on to nitrocellulose membranes (Millipore). Membranes were blocked for 1 h with 5% milk proteins in PBST (PBS+0.1% Tween 20) and subsequently incubated with mouse anti-human MMP8 (1:500 dilution; R&D systems; MAB9081), rabbit anti-MMP8 (1:500 dilution; Lifespan Biosciences; LS-C48493) or rabbit anti-PE (1:500 dilution; EZBiolabs) in 2% milk/PBST overnight at 4°C. Afterwards, membranes were incubated with HRP-labelled secondary antibodies (1:2000 dilution; Dakocytomation) in 2% milk/PBST, treated with commercial ECL reagents (Amersham Biosciences, Roosendaal, The Netherlands) and finally exposed to photographic film. Blots were then stripped with stripping buffer (Thermo Fisher Scientific) and reprobed with rabbit anti-glyceraldehyde-3-phosphate dehydrogenase (GAPDH; 1:5000 dilution; ITK Diagnostics, Uithoorn, The Netherlands).
Statistical significance of differences between groups was determined by paired t test, unpaired t test, Mann–Whitney U test, Wilcoxon signed rank test, or one-way analysis of variance followed by Dunnett's multiple comparison test using GraphPad Prism 4.0 or SPSS V.16.0. Results were considered significant when p<0.05.
Protease expression in IBD
MMP8 levels (figure 1A) were found to be increased in inflamed IBD intestinal tissue homogenates compared with non-inflamed IBD and control tissue, similar to MMP9 levels (see online supplementary figure S1B).19 Investigation of MMP8 levels by immunoblotting showed that the majority of the expressed MMP8 is the active form (figure 1C). There were no differences in MMP8 expression in tissue from patients with UC or CD, or in intestinal location (data not shown). There was a strong correlation between MMP8 level (Spearman's r=0.557, p<0.001) and MPO activity. Thus, both MMP8 and MMP9, the proteases necessary for the initial collagen-cleavage step, were present in the inflamed bowel specimens obtained from patients with IBD.
PE activity in IBD
As PE is responsible for cleaving the smaller collagen fragments into PGP, we measured PE activity in the same panel of IBD intestinal tissue homogenates. The activity of PE was similar in control tissue and inflamed and non-inflamed IBD samples (figure 1B). There was also no difference between tissue from patients with UC or CD, or in intestinal location (data not shown). This was confirmed by immunoblotting (figure 1C). In all tissues, a single band was detected at 81 kDa, which is the active PE form, as there is no proenzyme form.14
Protease expression in the intestine of patients with IBD
We were interested to determine which cells produce the proteases, MMP8, MMP9 and PE, and if they colocalise within the intestine, enabling generation of PGP from collagen. MMP9 was mainly present in infiltrating immune cells such as neutrophils and macrophages (figure 1D). Weak expression of MMP8 in epithelial cells in addition to expression in inflammatory cells was found in some patient samples (figure 1D), as reported previously.26 PE was expressed in both epithelial cells and inflammatory cells, including neutrophils (figure 1D). To confirm PE production by intestinal epithelial cells, HT29 and Caco2 cells were cultured in vitro. Both cell lines produced and secreted PE (data not shown).
PGP generation in the intestine of patients with IBD
Measurement of PGP and N-Ac-PGP in intestinal tissue homogenates showed that N-Ac-PGP levels were significantly higher in IBD intestinal tissue samples (figure 2A), while there was a trend towards increased PGP levels (figure 2B). We investigated whether PGP degradation was enhanced in the intestine of patients with IBD. Leukotriene A4 hydrolase (LTA4H) is capable of degrading PGP,27 and may also be increased during inflammation. LTA4H activity in intestinal tissue homogenates can be measured indirectly by measuring LTB4. There were no differences in LTB4 levels in inflamed versus non-inflamed or control intestinal tissue homogenates (online supplementary figure S2), and therefore no increase in LTA4H activity in IBD.
PMNs and PGP generation in IBD
During inflammation and collagen degradation, MMP8, MMP9 and PE are essential proteases involved in PGP generation, and they can all be produced by neutrophils.28 To investigate whether these specific proteases are increased in PMNs from patients with IBD, PMNs isolated from peripheral blood of healthy controls and patients were incubated for 6 h with medium. Subsequently, MMP8, MMP9 and PE levels were measured in the conditioned medium. Both MMP8 and MMP9 were significantly enhanced in IBD PMNs compared with healthy control PMNs (figure 3A,B), while the released PE activity was similar (figure 3C). This correlates with the data from the tissue homogenates: increased MMP8 and MMP9 at inflamed sites compared with non-inflamed/control samples, and similar PE activity. To investigate if the proteases released by the PMNs were capable of generating (N-Ac-)PGP ex vivo, PMN-conditioned medium was incubated with type I collagen. This showed that PMNs from patients with IBD are much more potent in forming N-Ac-PGP from collagen than healthy control PMNs (figure 3D). PGP levels were also increased, although not significantly (figure 3E). To examine if this difference in neutrophil function was a consequence of the activation state of the neutrophil, PMNs from healthy controls were exposed to the bacterial toxin, LPS. After LPS exposure, PMNs from healthy controls were capable of generating PGP from collagen (online supplementary figure S3). This suggests that, in areas with massive neutrophil infiltration in the intestine of patients with IBD, there is the potential to produce high amounts of (N-Ac-)PGP.
Proteases and PGP generation in the DSS-induced colitis model
To determine the role of PGP in intestinal neutrophilic inflammation by PGP neutralisation, we investigated the generation of PGP in the DSS-induced colitis model in mice. Because there are species differences in CXCR2-binding characteristics and signalling, we used huCXCR2 knock-in mice21 to mimic the human situation more closely.
MMP8, MMP9, PE activity and PGP levels were investigated during two 5-day cycles of 1.5% (w/v) DSS with a 10-day normal tap water period in between. The animals had clinicopathological signs of colitis, including moderate body weight loss (online supplementary figure S4A), bloody diarrhoea (online supplementary figure S4B), reduced colon length (online supplementary figure S4C), and increased histopathological scores (online supplementary figure S4D) including increased infiltration of neutrophils, assessed by MPO activity (online supplementary figure S4E), during these cycles. Similar to human IBD, there was no significant increase in intestinal PE activity in the DSS-induced colitis model (figure 4A,B), while MMP9 (both total and active) levels were elevated in the inflamed intestine (figure 4C,D). MMP8 was also slightly elevated (figure 4E) and mainly present in the active form (figure 4F). MMP9 was expressed in infiltrating leucocytes, and MMP8 and PE were found in both infiltrating leucocytes and epithelial cells (figure 5A). As found for human intestinal samples, the generation of both PGP and N-Ac-PGP was evident in intestinal samples (figure 5B,C). There was a strong trend towards increased (N-Ac-)PGP levels in DSS-induced colitis (day 8 vs day 0, p=0.09).
LTB4 levels also remained unchanged during the first DSS cycle (online supplementary figure S5A). The other neutrophil chemoattractants in mice, CXCL1 and CXCL2, were elevated during the first DSS cycle (online supplementary figure S5B,C), similar to CXCL8 in human IBD.29 So the protease expression pattern, (N-Ac)PGP formation and LTA4H activity in the DSS-induced colitis model were all similar to that found in IBD patient samples, making this model suitable for studying the effects of (N-Ac-)PGP neutralisation on neutrophil infiltration in the intestine.
Therapeutic intervention by PGP neutralisation
Because the (N-Ac-)PGP elevation during the first DSS cycle was similar to the elevation found in the intestinal IBD samples, we investigated the effect of PGP neutralisation in this first DSS cycle, by daily treatment with either a PGP-neutralising antibody27 or the complementary peptide sequence, arginine–threonine–arginine (RTR).30 PGP neutralisation did not have a profound effect on the mild reduction in body weight (data not shown). However, it caused amelioration of wasting of the disease, as judged by a reduction in the other clinicopathological characteristics of DSS-induced colitis, compared with their respective controls (PBS or isotype antibody treatment) (figure 6A). There were no effects of PGP neutralisation on control (water-treated) animals (data not shown). Both the DAI and the shortening of the colon (figure 6B) were significantly reduced at day 7. Histopathological analysis revealed a significant decrease in the histopathological scores due to PGP neutralisation (figure 6C,D). Moreover, investigation of neutrophil infiltration by immunohistochemistry (figure 6E) and MPO levels (figure 6F) showed that PGP neutralisation significantly reduced neutrophil infiltration in the colon of DSS-treated mice.
The levels of CXCL1 and CXCL2 (online supplementary figure S6A,B) and total and active MMP9 levels (online supplementary figure S7A,B) in the intestine were decreased by PGP neutralisation in DSS-induced colitis.
Neutrophils are rapidly recruited to sites of infection in response to ELR+ CXC chemokines, such as CXCL8 in humans and CXCL1and CXCL2 in mice.2 In IBD and DSS-induced colitis, these chemokines are elevated in the intestine.11 ,12 We now show that, besides these classic neutrophil chemoattractants, a collagen-derived tripeptide, PGP, also plays an important role in neutrophilic inflammation in IBD. PGP is generated from collagen by the combined action of MMP8, MMP9 and PE. Our studies identified a previously unrecognised role of these proteases in IBD.
We found that MMP8 and MMP9 are mainly expressed by inflammatory cells in the intestine, and levels of both are increased in IBD, similar to results of others. The other protease involved in the PGP generation cascade,6 PE, may be involved in peptide degradation during nutrient absorption in the gut.14 To our knowledge, this is the first report of an investigation of PE activity and protein levels in the intestine of patients with IBD. PE expression and activity were found in the intestine of patients with IBD as well as in control tissue, but there was no difference in inflamed versus non-inflamed or control. In contrast with MMP8 and MMP9, PE was mainly expressed by epithelial cells.
If MMP8 or MMP9 activity is the limiting step in the generation of PGP, one would expect more PGP generation during intestinal inflammation, as PE is already present in healthy intestinal tissue and MMP8 and MMP9 are greatly increased during intestinal inflammation. We indeed found a significant increase in N-Ac-PGP in intestinal tissue from patients with IBD, and there was also a trend towards increased PGP levels. Collagen type I is the type of collagen that is most abundantly found in the intestine.31 Human neutrophils can contain MMP8, MMP9 and PE and are capable of generating PGP from collagen type I on activation.28 Because circulating neutrophils from patients with IBD are more activated,32 we hypothesised that PMNs isolated from peripheral blood of such patients release more proteases and are more capable of generating PGP from collagen. Indeed we found that PMNs from patients with IBD release more MMP8 and MMP9 and have similar PE levels under unstimulated conditions than PMNs from healthy controls. Moreover, conditioned medium from PMNs obtained from patients with IBD are capable of producing PGP from collagen under unstimulated conditions, in contrast with conditioned medium from PMNs obtained from healthy controls. Activating healthy control PMNs with LPS led to increased MMP8, MMP9 and PE release from healthy control PMNs and PGP generation from collagen, characteristics similar to those of IBD patient PMNs. As PE is mainly expressed by epithelial cells, high concentrations of PGP could be produced in the epithelium, which in turn results in a chemotactic gradient. As a result, the neutrophils are directed towards the damaged epithelium, where commensal bacteria are triggering the intestinal wall.
LTB4, produced by LTA4H, is a powerful chemoattractant for neutrophils and is implicated in several chronic inflammatory disorders.33 LTA4H has recently been shown to be capable of degrading PGP, thereby acting as a both a proinflammatory and anti-inflammatory enzyme.27 Enhanced expression of LTB4 in intestinal mucosa from patients with IBD has been reported.34 LTA4H activity in inflamed intestinal tissue may therefore be involved in limiting PGP levels. The intestinal levels of LTB4 in the patients with IBD in this study were similar to those in colorectal cancer controls, which indicates that there was no increase in LTA4H activity in IBD.
N-Ac-PGP is a far more potent chemoattractant for neutrophils than PGP.7 Incubation of IBD PMN-conditioned medium resulted mainly in N-Ac-PGP formation from collagen type I, indicating that IBD neutrophils also release the enzyme necessary for acetylation of PGP. Recent work by our group shows that the PMNs isolated from peripheral blood from patients with IBD (also used in this study) have increased migratory capacities towards CXCL8 compared with healthy control PMNs, probably due to the increased expression of CXCR1 and CXCR2 (Overbeek et al, unpublished work). Therefore PGP levels, and especially N-Ac-PGP levels, may play an important role in neutrophilic infiltration in IBD, as neutrophils from patients with IBD may be more strongly attracted to (N-Ac-)PGP.
To study the pathophysiological role of PGP in neutrophilic inflammation in the colon, we used DSS-induced colitis in mice. This widely used IBD model depends largely on MMP9 protease activity, as MMP9-deficient mice are resistant to DSS-induced colonic inflammation,15 and MMP inhibition reduced clinical features.16 With regard to the other components involved in the PGP generation cascade, there were striking similarities to human IBD. There was an increase in active MMP8 in colonic tissue from DSS-treated mice, and PE was present. There was a strong trend towards increased (N-Ac-)PGP levels. DSS-induced colitis is characterised by a large CXCR2-dependent influx of neutrophils17 ,18 and is therefore highly suitable for studying the role of PGP in neutrophilic infiltration in the intestine. Neutralisation of PGP by daily treatment with PGP antibodies or the PGP antagonist, RTR, led to a significant reduction in the DAI and reduced shortening of the colon. Moreover, PGP neutralisation led to a significant reduction in infiltrating neutrophils in the intestine of DSS-treated mice.
PGP induces the release of both CXCL8 and MMP9 of human PMNs in vitro,20 ,35 and an increase in CXCL1 was seen on N-Ac-PGP-mediated neutrophilic infiltration in the lung.23 Interestingly, we found that the DSS-induced elevation of both CXCL1 and CXCL2 in the intestine was reduced by PGP neutralisation. Also, PGP neutralisation in DSS-induced colitis led to a significant reduction in elevated intestinal MMP9 levels. This suggests that PGP-induced activation of neutrophils, reflected by increased CXCL1, CXCL2 and MMP9 levels, also occurs in the intestine. A more profound activation of neutrophils by N-Ac-PGP in the local intestinal micro environment of patients with IBD or DSS-treated mice may explain the beneficial effect of PGP neutralisation on intestinal inflammation in IBD.
In conclusion, both the proteolytic cascade that generates PGP from collagen and (N-Ac-)PGP itself are present in the intestine (figure 7). (N-Ac-)PGP-guided neutrophilic infiltration, either by a direct chemotactic effect on circulating neutrophils or activation of resident immune cells, plays an important role in intestinal inflammation. This indicates a vicious circle of neutrophil-mediated intestinal collagen proteolysis and subsequent PGP-guided infiltration of neutrophils in the intestine, and opens up new approaches to the treatment of sustained inflammation in IBD.
Review history and Supplementary material
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Contributors PJK, SAO, GF and ADK, study concept and design; PJK, SAO, SB, SCW, MAR, CWJ and PLJ, acquisition and analysis of data; PJK and ADK, writing of the manuscript; HWV, AAteV, JEB, JG, RWS and JAWK, technical and material support; MEM, PAJH, HWV, JEB, critical revision of the manuscript for important intellectual content; PLJ, JEB, GF and ADK, obtaining funding; ADK, study supervision.
Funding This study was performed within the framework of Dutch Top Institute Pharma (T1.103) and was supported in part by grants from the National Heart, Lung and Blood Institute (HL07783, HL90999 and HL087824 to JEB) and the Cystic Fibrosis Foundation (R464-CR11 to PLJ). MAR was supported by a Mosaic grant from the Netherlands Organization for Scientific Research (017.008.029). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Heart, Lung and Blood Institute or the NIH.
Competing interests None.
Ethics approval The medical ethics committee of the Leiden University Medical Centre approved the intestinal tissue samples study, which complied with the Helsinki Declaration. All protocols using fresh peripheral blood were approved by the local ethics committees of the Amsterdam Medical Centre and Utrecht Medical Centre.
Patient consent Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.
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