Cathelicidin-related antimicrobial peptide modulates the severity of acute pancreatitis in mice

Abstract

The present study aimed to investigate the immunomodulatory effects of mouse cathelicidin-related antimicrobial peptide (CRAMP) on experimental acute pancreatitis (AP). AP is a common clinical condition characterized by acute abdominal inflammation. Innate immune cells and mediators are intrinsically linked to the pathogenesis of AP. Cathelicidins are innate immunity-derived antimicrobial peptides that exert immunomodulatory effects on various host cells. However, how cathelicidins are involved and modulate the severity and inflammatory responses of AP remains unclear. In the present study, the mouse CRAMP gene-deficient cnlp^−/− mice and their wild-type C57BL/6J littermates were induced with AP by multiple hourly injections of supramaximal doses of caerulein. Serum amylase levels, pancreatic myeloperoxidase activity and histological examination were performed in order to determine the disease severity and the levels of inflammatory cytokines. Disease severity and inflammatory markers were subsequently evaluated in the control mice, cnlp^−/− C57BL/6J mice with AP, and wild-type C57BL/6J mice with AP. The results demonstrated that cnlp^−/− mice exhibited a more severe phenotype and inflammatory response following AP induction compared with the wild-type mice, as evidenced by increased serum amylase levels, pancreatic myeloperoxidase release, and early inflammatory mediator tumor necrosis factor-α production. Histological examination confirmed that CRAMP deficiency worsened the pancreatic inflammatory condition. These results indicate that CRAMP may be considered a novel modulatory mediator in mouse experimental AP.

Introduction

Acute pancreatitis (AP) is a common abdominal inflammatory disease for which a specific clinical treatment remains elusive (1,2). The majority of patients with AP exhibit a mild form of the disease; however, 20–25% of patients suffer a severe episode and consequently may develop multiple organ dysfunction syndrome, a main cause of AP-associated mortality (3,4). Alcoholism and gallstones are the most common etiological factors, which lead to intrapancreatic trypsinogen activation and cellular injury of the pancreas (2,5). Innate immune cells and mediators have important roles in the pathogenesis of AP (6,7), and prognosis of the disease is directly associated with the intensity of inflammation. Immune cell infiltration and elevated serum levels of mediators, including tumor necrosis factor (TNF)-α and interleukin (IL)-1β, are used as markers of inflammatory responses (8). Recently, antimicrobial peptides (AMPs), particularly α-defensins, have been implicated in AP (9). AMPs are innate immunity-derived peptides, which are primarily expressed by epithelial cells and infiltrating immune cells in mammals under steady state or during inflammation (10). AP is an inflammatory disorder, and is therefore associated with altered permeability of the AMP-producing cells, thus suggesting a potential role for AMPs in this condition.

Among AMPs, cathelicidins are pleiotropic AMPs that possess broad-spectrum antimicrobial activities and have a major role in regulating local inflammation and immunity (11,12). Cathelicidins are characteristically cationic and share a conserved N-terminal pro-region, which is termed the cathelin domain, and a variable C-terminal antimicrobial domain. A single cathelicidin is found in humans (hCAP18/LL-37) and its orthologs in the rat and mouse are rat cathelicidin-related antimicrobial peptide (CRAMP) and mouse CRAMP, respectively (13,14). In addition to their antimicrobial activities, cathelicidins have been reported to exert modulatory effects on various host cells, notably epithelial and immune cells (15–18). Cathelicidins contribute to immune cell recruitment and activation, cytokine production, modulation of inflammatory responses during inflammatory bowel diseases and gastrointestinal inflammation (12,18). However, the role of CRAMP in AP remains clear.

AP is associated with complex episodes of inflammation of the pancreatic acinar cells and distant organs. While the cellular and molecular regulatory mechanisms underlying AP pathogenesis remain to be fully elucidated for the identification of a curative treatment, exploration of novel innate immunomodulatory mediators may yield a promising outcome (19). Therefore, the present study investigated the potential effects of CRAMP on caerulein-induced experimental AP in mice. The results support a modulatory role of CRAMP in AP, and suggest CRAMP may be a potential therapeutic target for future investigation.

Materials and methods

Animals

Male C57BL/6J (Su Pu Si Biotechnology Co., Ltd., Suzhou, China) and CRAMP-deficient cnlp^−/− mice (C57BL/6J background; age, 8 weeks; The Jackson Laboratory, Sacramento, CA, USA) were maintained at the Animal Housing Unit of Jiangnan University (Wuxi, China) under a controlled temperature (23–25°C) and a 12 h light/12 h dark cycle. All of the mice were provided with standard laboratory chow and water ad libitum. All experimental protocols were approved by the Animal Ethics Committee of Jiangnan University, and were performed in accordance with the guidelines therein.

Reagents

Caerulein and tetramethylbenzidine substrate were used for enzyme-linked immunosorbent assay (ELISA) assays and were purchased from Sigma-Aldrich (St. Louis, MO, USA). Amylase and myeloperoxidase (MPO) activity measurement kits were purchased from the Jiancheng Bioengineering Institute (Nanjing, China). Mice TNF-α and mice monocyte chemotactic protein (MCP)-1 ELISA kits were obtained from Biolegend, Inc. (San Diego, CA, USA). All other reagents were supplied locally by the material library of Jiangnan University and were purchased from National Medicine Group Chemical Reagent Co., Ltd. (Shanghai, China).

Induction of AP

Mice were randomly assigned into the control and experimental groups (n=8). The groups were as follows: CRAMP gene knockout (cnlp^−/−) mice and wild-type C57BL/6J mice with the same genetic background were randomly assigned into the cnlp^−/− control, cnlp^−/− mice with AP group [AP (cnlp^−/−)] and C57BL/6J mice with AP group [AP (C57)]. The mice received hourly intraperitoneal injections with normal saline or saline containing caerulein (50 µg/kg) for 10 h to induce AP. A total of 1 h after the final injection, the mice were sacrificed with a lethal dose of pentobarbitone sodium (100 mg/kg). The experiments were repeated three times. Blood samples were collected in sterilized centrifuge tubes, were centrifuged to separate the serum, and were stored at −80°C. The harvested pancreatic tissue samples were stored at −80°C for subsequent measurements of MPO activity, and cytokine and chemokine levels.

Serum amylase measurements

Serum was collected by allowing the blood to coagulate at ambient temperate for 25 min, and subsequently centrifuging the samples at 3,000 × g for 10 min at 4°C. The supernatant was then collected for analysis. An iodine-starch colorimetric method was used to measure serum amylase levels. Briefly, serum samples were incubated with 0.5 ml pre-warmed substrate buffer for 7.5 min at 37°C. Absorbance was measured, following the addition of 0.5 ml iodine and 3 ml ddH₂O to the mixture, at 660 nm using a UV-2450 UV-VIS spectrophotometer (Shimadzu Corporation, Kyoto, Japan).

MPO activity

MPO activity was evaluated using an MPO assay kit according to the manufacturer's protocol. Pancreatic tissues (5%) were homogenized in 0.9% saline using an IKA homogenizer (Straufen, Germany). Absorbance was analyzed using a UV-2450 UV-VIS spectrophotometer (Shimadzu Corporation) at 460 nm within 10 min and MPO activities are expressed as units/g tissue.

ELISA assays of inflammatory mediators

Pancreatic homogenates were assayed for MCP-1 and TNF-α levels using sandwich ELISA kits. Previous procedures validated by our group were adopted, according to the manufacturer's protocols. Absorbance was measured at 450 nm within 30 min, using an automated microplate reader (Multiskan™ GO; Thermo Fisher Scientific Oy, Vantaa, Finland). TNF-α and MCP-1 concentrations were calculated based on the absorbance measurements, and are expressed as pg/ml.

Histological examination

Freshly harvested pancreatic samples were fixed with 4% paraformaldehyde overnight. The tissues were then washed with ddH₂O, dehydrated with gradient ethanol solutions and embedded in paraffin and cut into 5 µm sections. The sections were subsequently stained with hematoxylin/eosin (H&E). Pancreatic injury was examined under a DM2000 light microscope (Leica Microsystems GmbH, Wetzlar, Germany) at ×200 magnification, and was evaluated based on acinar cell injury, inflammatory cell infiltration and structural changes, which are markers of tissue damage and inflammation.

Statistical analysis

Statistical analysis was performed by independent t-test to determine if there was a difference between MPO activity levels in the control and AP (C57) group, AMY levels between AP (cnlp^−/−) and AP (C57) groups. When multiple comparisons were made, by one-way analysis of variance using GraphPad Prism (version 5; GraphPad Software Inc., San Diego, CA, USA). Tukey's honest significant difference test was performed as a post-hoc test. P<0.05 were considered to indicate a statistically significant difference.

Results

Effects of CRAMP deficiency on serum amylase levels during AP

Serum amylase is measured as a sensitive biochemical marker of AP, which is released due to pancreatic acinar cell damage. Serum amylase levels were elevated in the wild-type (P<0.001) and cnlp^−/− AP (P<0.001) mice compared with in the control mice. In addition, CRAMP-deficient mice exhibited more pronounced serum amylase levels compared with the wild-type mice (P<0.05; Fig. 1). These findings suggest that CRAMP may have a beneficial role in protecting mice against AP.

Figure 1.

Effects of cathelicidin-related antimicrobial peptide deficiency (cnlp^−/−) on serum amylase (AMY) levels. Data are presented as the mean + standard error of the mean. ^***P<0.001 caerulein-treated mice vs. control; ^#P<0.05 caerulein-treated cnlp^−/− mice vs. caerulein-treated C57BL/6J mice. AP, acute pancreatitis; CON, control; C57, C57BL/6J wild-type mice.

Effects of CRAMP deficiency on pancreatic MPO release

Pancreatic MPO levels were evaluated as an indicator of neutrophil infiltration into tissues during AP. Caerulein hyperstimulation resulted in increased pancreatic MPO levels in the wild-type (P<0.05) and cnlp^−/− mice (P<0.01; Fig. 2). This increase in MPO was more significant in the pancreatic tissues of the cnlp^−/− mice compared with the wild-type mice (P<0.05; Fig. 2). These results suggest that CRAMP may be involved in early neutrophil recruitment to the pancreas and regulating MPO activities during AP.

Figure 2.

Effects of cathelicidin-related antimicrobial peptide deficiency (cnlp^−/−) on pancreatic myeloperoxidase (MPO) levels. Data are presented as the mean + standard error of the mean. ^*P<0.05 vs. the control mice (CON); ^**P<0.01 vs. CON; ^#P<0.05 vs. caerulein-treated cnlp^−/− mice. AP, acute pancreatitis; C57, C57BL/6J wild-type mice.

Effects of CRAMP deficiency on pancreatic production of inflammatory mediators

As AP propagates it is associated with enhanced production of inflammatory cytokines and chemokines at the tissue level. Therefore, the present study examined the levels of known early mediators of AP, including TNF-α and MCP-1. As shown in Fig. 3A and B, experimental AP is associated with increased levels of pancreatic TNF-α (P<0.001) and MCP-1 (P<0.01). A further increase in TNF-α levels (all P<0.05), but not MCP-1 levels, was observed in the pancreas of cnlp^−/− mice compared with in the C57BL/6J wild-type AP mice (Fig. 3A and B). These results indicate that CRAMP selectively modulates pancreatic cytokine production during AP.

Figure 3.

Effects of cathelicidin-related antimicrobial peptide deficiency (cnlp^−/−) on the pancreatic production of inflammatory mediators (A) tumor necrosis factor (TNF)-α and (B) monocyte chemotactic protein (MCP)-1. Data are presented as the mean + standard error of the mean. ^*P<0.05 vs. the control mice (CON); ^**P<0.01 and ^***P<0.001 vs. CON; ^#P<0.05 vs. caerulein-treated cnlp^−/− mice. AP, acute pancreatitis; C57, C57BL/6J wild-type mice.

Effects of CRAMP deficiency on tissue damage during AP

Pancreatic injury in mice with AP was evaluated by H&E histological examination. The wild-type and CRAMP-deficient cnlp^−/− mice induced with caerulein hyperstimulation exhibited pronounced pancreatic edema, enhanced neutrophil infiltration into the pancreas, and pancreatic morphological injuries, as compared with the control mice (Fig. 4A–C). Furthermore, pancreatic injury in the cnlp^−/− mice (Fig. 4B) was more severe than in the wild-type mice (Fig. 4C). This histological analysis confirmed that CRAMP alleviates pancreatic injury and inflammation.

Figure 4.

Histological examination of tissue damage in the cathelicidin-related antimicrobial peptide-deficient (cnlp^−/−) and wild-type C57BL/6J mice (C57) with acute pancreatitis (AP) using hematoxylin/eosin staining. Representative images (magnification, 200×) from each group from two independent experiments are presented. (A) Wild-type control mice (B) cnlp^−/− mice with AP (C) wild-type mice with AP.

Discussion

The present study demonstrated that mouse CRAMP is a novel modulatory mediator during AP, which is particularly associated with local pancreatic inflammation. The cnlp^−/− C57BL/6J mice developed a more severe phenotype and inflammatory responses, as compared with their wild-type littermates induced with AP. In addition, the cnlp^−/− C57BL/6J mice exhibited more pronounced serum amylase levels, pancreatic MPO release and TNF-α production than the wild-type mice. These data indicated that CRAMP may have a modulatory role in experimental AP.

A cascade of cellular events, including activation of intra-acinar enzymes, release of inflammatory mediators and cytokines, acinar cell apoptosis, and pancreatic microcirculation disorder have been reported to underlie the pathogenesis of AP (20–23). However, AP pathogenesis remains to fully elucidated. AMPs represent novel mediators of the condition. Intestinal α-defensin (α-defensin-5 and α-defensin-7) levels, but not CRAMP, were shown to be elevated in aged rats with AP, and were associated with more severe local inflammation (9). The role of cathelicidins (human LL-37 and mouse CRAMP) has been particularly documented in other inflammatory processes (24); however, its role is unknown in AP. Therefore the present study investigated cathelicidins as a potential immunomodulatory mediator in a mouse model of experimental AP, using CRAMP-deficient cnlp^−/− mice.

The results of the present study demonstrated that cnlp^−/− mice with AP exhibited more pronounced acinar cell injury, as measured by serum amylase levels, MPO activity and TNF-α production, as compared with the wild-type AP mice. Immune cell infiltration into the tissues and production of inflammatory cytokines (chemokines) are key pathological events that determine, to a large extent, disease severity (25,26). During AP, neutrophils are the first-line innate immune cells recruited to the pancreas. TNF-α, which is derived predominantly from activated macrophages, acts via cell membrane-bound receptors (27) to induce proinflammatory gene expression of IL-1, IL-6, IL-8 and itself, thereby causing pancreatic tissue necrosis and further migration of leukocytes (28). The prototypic CC chemokine MCP-1 is an early mediator associated with chemo-attraction of macrophages and further propagation of local to systemic inflammation (29). Although both TNF-α and MCP-1 are significantly elevated in the pancreas of cnlp^−/− and wild-type AP mice (Fig. 3), only TNF-α levels were significantly higher in the cnlp^−/− mice than the wild-type mice, thus suggesting that the regulatory effects of CRAMP may be selective towards TNF-α-producing cells in the pancreas.

The present study detected a more resistant phenotype during AP due to the C57BL/6J genetic background of cnlp^−/− and wild-type mice. Different mouse strains have exhibited varied susceptibility to caerulein-induced AP. Serum amylase and TNF-α production in BALB/c mice are significantly higher than in C57BL/6J mice upon AP induction (unpublished data). Despite this intrinsic variation of responses, CRAMP deficiency still worsens pancreatic inflammatory conditions, further suggesting its modulatory role in AP.

In conclusion, the present study is the first, to the best of our knowledge, to demonstrate that cathelicidins exert immune regulatory effects on AP in mice (Fig. 5). In addition, the present study provides novel evidence for the effective prevention and treatment of AP in clinical practice.

Figure 5.

Graphical summary of the modulatory effects of cathelicidin-related antimicrobial peptide (CRAMP) on caerulein-induced experimental acute pancreatitis (AP). CRAMP modulates amylase release from acinar cells, myeloperoxidase (MPO) release from neutrophils, and the production of inflammatory cytokines during AP. TNF-α, tumor necrosis factor-α; MCP-1, monocyte chemotactic protein-1.

Abbreviations

AP

acute pancreatitis

AMP

antimicrobial peptide

CRAMP

cathelicidin-related antimicrobial peptide

MCP

monocyte chemotactic protein

MPO

myeloperoxidase

IL

interleukin

TNF

tumor necrosis factor