Background
Inflammatory bowel disease (IBD) is the result of a chronic intestinal inflammatory response. While the exact pathogenesis of IBD remains incompletely understood, it is likely that the initiation of the immune response is triggered by luminal factors [
1]. The nature of these initiating agents is unclear, but both orally ingested nutrients and microbial agents have been implicated [
2]. It is widely believed that an impaired barrier function, and in particular a defect of the mucus layer, leads to an increased exposure of the mucosal immune system to luminal antigens. In genetically susceptible individuals, this results in an inappropriate and unrestrained inflammatory response [
3,
4].
We have recently shown that both PC and lysophosphatidylcholine (LPC) but neither phosphatidylethanolamine (PE) nor sphingomyelin (SM) are decreased in the mucus of patients with ulcerative colitis (UC) and that the oral substitution of PC using slow release preparations is beneficial [
5‐
7]. How luminal PC influences the clinical course of UC is not yet known, but two scenarios are possible. First, because of its hydrophobic property, PC coats the mucus layer, thereby preventing the contact of luminal bacteria to the mucosa [
5,
8,
9]. With respect to this, luminal PC has been shown to synergize with conjugated primary bile salts in the binding of luminal endotoxin, which in turn leads to a suppressed inflammation beyond the mucosal surface [
10]. On the other hand, we could recently demonstrate that PC per se has anti-inflammatory properties. PC has been shown to inhibit membrane-dependent actin assembly and TNF-α-induced MAPkinase and NF-κB activation [
11]. In light of these results, we hypothesized that luminal PC might be integrated into the plasma membranes of enterocytes and in turn modulate the signalling state of the mucosa in the human intestine. This assumption is further substantiated by studies using an
in vitro phagosome system [
12,
13] which show that exogenous PC is indeed involved in the networks which inhibit pro-inflammatory signalling in membranes.
IBD encompasses two chronic intestinal diseases, Crohn's disease (CD) and UC, which differ in their microscopic and macroscopic features although their symptoms are similar [
14]. Ulcerative lesions in IBD are accompanied by a prominent infiltrate of inflammatory cells including T lymphocytes, macrophages, neutrophils, and mast and plasma cells [
15]. Mechanisms involved in the recruiting and activating of these inflammatory cells are thought to encompass a complex interplay of inflammatory mediators. This is reflected by the elevation of various chemokines in the serum and mucosa of IBD patients (for review see [
16]). Over 40 human chemokines are now acknowledged, each with its own specific pattern of cellular chemotaxis. The chemokine family is categorised into four groups depending on the spacing of their first two cysteine residues [
17]. Cumulative studies demonstrate that all four types of chemokines are involved in the development of IBD [
16]. The expression level of pro-inflammatory chemokines differed significantly between IBD patients and controls. Up-regulated chemokine expression in human biopsies correlated with increasing activity of the disease [
16]. Pro-inflammatory cytokines such as TNF-α and interleukin 1β (IL-1β) up-regulate the transcription of chemokine genes and hence the synthesis of chemokines themselves through the activation of NF-κB [
18,
19]. As TNF-α has been shown to be an important player in the inflammatory process of IBD [
20], we previously established a model cell system with human intestinal epithelial cells (Caco-2) which we stimulated with TNF-α to induce a pro-inflammatory response [
11]. Using this system, we now analysed the effect of various PC species on the transcriptional levels of selected marker genes. After PC treatment, the TNF-α induced up-regulation was significantly reduced in a time- and dose-dependent manner depending on the fatty acid composition. PC was effective when applied to the apical side of polarized Caco-2 cells if they were stimulated from the basal side. We could show that the TNF-α effect was dependent on NF-κB activity and not due to inhibition of the binding of TNF-α to its receptor. PC treatment changed the compartmentation of TNF-α-R1 and TNF-α-R2 to lipid rafts, which is a possible mechanism of action.
Methods
Lipids and reagents
TNF-α was obtained from Promega (Mannheim, Germany) and dissolved in endotoxin-free water containing 1% BSA from Sigma (Deisenhofen, Germany). Aliquots of 10 μg/ml were stored at -70°C. The NF-κB inhibitor SN 50 was from Calbiochem (San Diego, USA). PC 18:2/18:2 (1,2-dilinoleoyl-glycero-3-PC), PC 16:0/16:0 (1,2-dipalmitoyl-glycero-3-PC), PC 16:0/18:2 (1-palmitoyl-2-linoleoyl-glycero-3-PC), LPC 16:0 (1-palmitoyl-glycero-3-PC), PE 16:1/16:1 (1,2-dioleyl-glycerol-3-PE) were from Sigma (Deisenhofen).
Cells and bacteria
Caco-2w cells are a sub-clone of the human Caco-2BBe and were selected because of their well-differentiated phenotype. They were provided by J. R. Turner (University of Chicago). Cells were grown at 37°C and 5% CO
2 in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% heat-inactivated fetal calf serum, 1% non-essential amino acid, and antibiotics (55 IU/mL penicillin and 55 μg/mL streptomycin). Vero cells (American Type Culture Collection; ATCC) were propagated in Dulbecco's Modified Eagle's Medium (DMEM) supplemented with 5% fetal bovine serum and antibiotics (55 IU/mL penicillin and 55 μg/mL streptomycin). For full polarization cells were grown for 14 d on 2.5 cm, 0.4 μm pore size Transwell polycarbonate filters (Costar, Cambridge, USA) as previously described [
21].
Gene expression analyses by RT-PCR quantification
Caco-2 cells were grown under standard conditions in 6-wells for 48 h to 90% confluence and washed in Dulbecco's modified Eagle's medium without serum. Then they were incubated with 10 ng/mL recombinant human TNF-α (RnD Systems, Wiesbaden-Nordenstadt, Germany) and different PC species for various times at 37°C. Approximately 1 × 10
6 cells were collected in 300 μl lysis buffer from the MagnaPure mRNA Isolation Kit I (RAS, Mannheim, Germany) and mRNA was isolated with the MagnaPure-LC device using the mRNA-I standard protocol. RNA was reverse transcribed using AMV-RT and oligo- (dT) as the primer (First Strand cDNA synthesis kit, RAS), according to the manufacturer's protocol, in a thermocycler. Primer sets specific for the sequences of the selected genes optimised for the LightCycler (RAS) were developed and provided by SEARCH-LC GmbH, Heidelberg
http://www.search-lc.com. The PCR was performed with the LightCycler FastStart DNA Sybr GreenI kit (RAS) according to the protocol provided in the parameter specific kits. To control for the specificity of the amplification products, a melting curve analysis was performed. No amplification of unspecific products was observed. The copy number was calculated from a standard curve obtained by plotting known input concentrations of four different plasmids at log dilutions to the PCR cycle number at which the detected fluorescence intensity reaches a fixed value. This was done to reduce variations due to handling errors over several logarithmic dilution steps. To correct for differences in the content of mRNA, the calculated copy numbers were normalised according to the average expression of two housekeeping genes (Cyclophilin B and β-Actin). Values were thus given as input adjusted to the copy number per μl of cDNA.
Transient transfection and reporter assays
Caco-2 cells were seeded in 12-wells, grown to a >95% confluency and transiently transfected with a NF-κB-dependent luciferase reporter plasmid according to the manufacturer's instructions (Stratagene, La Jolla, USA). Cells were then co-treated in medium with or without TNF-α (10 ng/ml) and with a 200 μM solution of different PCs for 4 h at 37°C 20 h after transfection. In pre-treatment experiments, cells were first incubated for 10 minutes with 200 μmol PC, washed, and afterwards stimulated with TNF-α (10 ng/ml) only. Luciferase activity was assayed using the Luciferase Assay Kit (Stratagene) according to the manufacturer's directions and detected with a Fluorostar Optima (BMG Labtech, Offenburg, Germany). Each transfection was performed in triplicate and repeated at least three times.
Flow Cytometry
A 25 μl volume of washed cells (60% density, 2*105 cells), either pre-treated with a 200 μmol PC or left untreated, was incubated with 10 μl of biotinylated TNF-α (10 ng/mL) for 60 min at 4°C. Biotinylated soybean trypsin inhibitor was used as negative control. A 10 μl volume of avidin-FITC reagent was then added to each tube and incubated for an additional 30 min at 4°C in the dark. The cells were washed twice with 2 ml of 1× RDF1 buffer to remove unbound avidin-fluorescein and resuspended in 600 μl of 1× RDF1 buffer. The sample was then subjected to flow cytometric analysis by using 488 nm wavelength laser excitation (Beckman Coulter). As a test of specificity, TNF-α biotin was neutralized with an anti-TNF-α antibody and then added to the cells to block nonspecific and specific binding of TNF-α biotin.
Preparation of DRMs
Detergent extraction with Triton X-100 was performed as described [
22]. Cells were grown in 3.5 cm dishes, transfected with TNF-α-R1 and TNF-α-R2 (provided by J. R. Turner, University of Chicago) and 10–12 h later washed once with PBS and scraped on ice into 1.5 ml homogenisation buffer (250 mM Sucrose, 10 mM Hepes, 2 mM EDTA). After centrifugation (5 min at 2000 rpm), cell pellets were homogenised in a homogenisation buffer containing 20 μg/ml each of chymostatin, leupeptin, antipain and pepstatin A (Sigma) through a 26 G needle and centrifuged for 5 min at 3000 rpm. The resulting supernatant was subjected to extraction for 30 min at 4°C in 1% Triton X-100. The extracts were adjusted to 40% OptiPrep (Axis-Shield, Oslo, Norway) and overlaid in a TLS 55 centrifugation tube with 30% OptiPrep/TNE and TNE (25 mM Tris-HCl, pH 7.4, 150 mM NaCl, 2 mM EDTA old protocol/25 mM Tris-HCl, pH 10.8, 150 mM NaCl, 5 mM EDTA). The gradients were centrifuged at 400000 g in a Beckman SW41 rotor for 20 h at 4°C. Fractions were obtained and used for Western blotting as described [
23]. Monoclonal antibodies against TNF-α receptor 1 (TNF-α-R1) were from Sigma and TNF-α receptor 2 (TNF-α-R2) from Alexis Biochemical (Lörrach, Germany); monoclonal antibodies against the Src-like kinase Yes were supplied from Transduction Laboratories (Lexington, K Y); and against Flotillin-1 came from BD Bioscience (Heidelberg, Germany).
Statistical analysis
All values are reported as mean and standard deviation (SD) or standard error of the mean (SEM). For homogeneity of variance, ANOVA was applied. Significance levels between single groups (medium, +TNF-α, +TNF-α +phospholipid) were analysed using Tukey's post-hoc test. Probability values of p < 0.05 were set as a threshold for statistical significance.
Discussion
The data we have presented here further strengthens the evidence that the application of exogenous PC has anti-inflammatory effects. Firstly, we could confirm that different PC species can inhibit TNF-α-induced NF-κB activation. LPC functioned in the same way, whereas PE was not effective. The effect of PC was not merely transient but instead persisted for at least for 2 h. Consistent with previous results [
11], we could demonstrate that the effect is dose dependent. Interestingly, PC 16:0/16:0 was less effective than species with unsaturated fatty acid side chains. As human mucus is made up of more than 90% PC species with one unsaturated fatty acid side chain (PC 16:0/18:1; PC 16:0/18:2; PC 18:0/18:1 and PC 18:0/18:2) [
5], it is intriguing to speculate that this might represent an optimal mixture for controlling the inflammatory response. The hypothesis deduced from this is that mucus PC might be a source for membrane PC in enterocytes and thus influence membrane-dependent signalling of the mucosa cells.
Clinical and animal as well as in vitro data further support the anti-inflammatory effect of PC. We and others have previously shown that PC inhibits actin polymerisation on isolated phagosomes as well as in macrophages and Caco-2 cells [
11,
12]. In the latter model, it also inhibits activation of the MAPkinases ERK and p38, which are upstream of NF-κB [
11]. Many animal studies support that PC is protective against pro-inflammatory conditions. With respect to this, it as been shown that it prevents mucosal injury induced by acids, NSAIDs or bile acids [
9,
31‐
39]. Parenteral administration of PC or LPC has been demonstrated to increase survival and improve inflammation in animal models of acute septic shock and endotoxemia [
40‐
42]. Interestingly, there is a sudden overproduction of TNF-α in acute septic shock which triggers hypotension, circulatory collapse, and the widespread inflammation seen in this clinical condition [
43]. Various species of LPC seem to protect against such a condition [
42]. TNF-α is also thought to be an important agent in the colonic inflammation of patients with ulcerative colitis (UC). There is an increased density of TNF-α immunoreactive cells in the mucosa of UC patients with actual inflammation and there is an increased concentration of TNF-α in faeces, mucosa biopsies and serum of actively ill patients [
44‐
46]. Most importantly, clinical studies have revealed that an anti-TNF-α strategy can be successful in treating those patients; therefore, this strategy is now integrated in daily clinical practice [
47]. Two clinical studies on patients with ulcerative colitis have been performed which show a therapeutic benefit by adding PC in the form of slow release preparations [
6,
7]. In these studies, PC was applied in the form of soy lecithin with a considerable amount of PE. PE can be metabolised to PC via methylation and therefore serves as an additional source for PC within the cell. PE is also a known source for the endocannabinoid system, which influences inflammatory reactions as well [
48]. However, our data show that exogenous PE has no significant effect on TNF-α-induced activation. This probably means that it is not the effective component of the preparation used in the clinical trials.
TNF-α exerts its functions through two distinct receptors, TNF-α-R1 (CD120a) and TNF-α-R2 (CD120b). After binding TNF-α, TNF-α-R1 recruits a death domain (DD)-containing adaptor molecule, namely the TNF-α-R1-associated death domain protein (TRADD). TRADD serves as a platform for recruiting additional mediators [
49]. It binds the DD-containing Ser/Thr kinase receptor-interacting protein (RIP) and TNF-receptor-associated factor 2 (TRAF2). This TRADD-RIP-TRAF2 complex initiates the pathway leading to NF-kB activation [
50‐
52]. How might exogenous PC function in this regulation?
1. It could be speculated that PC or LPC inhibits the association of TNF-α to its receptor. To exclude such an effect, we performed experiments in which the cells were treated with PC before TNF-α stimulation and quantified the binding of TNF-α to its receptor by FACS. FACS analysis could detect no quantitative differences between PC or LPC treated and non-treated cells. This makes a decreased receptor binding unlikely.
2. It has been previously suggested that TNF-α receptors, upon substrate binding, might be endocytosed and that the signalling response occurs in endosomes, as demonstrated in other receptors such as the β2-adrenergic receptor, the endothelin receptor and many other G-coupled protein receptors [
53‐
56]. Thus it has been speculated that the integration of PC into cellular membranes might affect endocytosis and consequently signalling. However, we could show by FACS analysis that the surface expression of TNF-α receptors was unchanged after PC treatment. This makes an influence of PC on endocytosis also unlikely.
3. A third scenario seems more likely. Mammalian membranes are lipid bilayers consisting of 300–400 different lipid species that are ordered in vertical and lateral dimensions. This order is maintained with the help of a highly regulated concert of enzymes. Adding exogenous lipids would lead to a change in the lipid assembly of the membrane and therefore would influence membrane-dependent processes. We have previously speculated that PC might be present in a freely mobile form and a pool that is attached to proteins [
11]. Proteins that bind selectively to PC have been described (e.g., START, C1 or C2 domain structures), of which a large number are involved in signalling [
57,
58]. Adding PC might shift the balance between the free and the bound fractions. Normally in cells the bulk of PC is in the outer leaflet of the membrane. It is therefore also possible that addition of PC might induce a higher concentration of PC on the inner leaflet. There it could interfere with selected signalling proteins such as MAP kinases or others involved in NF-κB activation. However, it has to be mentioned that the role of NF-κB is more complex in regulating the answer of the intestinal epithelium to luminal agents. NF-κB has been shown to regulate protective factors as well, including inducible beta defensins [
59]. Epithelial-cell-specific inhibition of NF-kB through conditional ablation of NEMO (IKKgamma) led to an increased apoptosis of colonocytes, impaired expression of antimicrobial peptides and translocation of bacteria into the mucosa [
60]. NF-κB therefore seems to be a regulator for the intestinal immune homoeostasis and the tuning of its activity by many mechanisms appears crucial in preventing inflammation [
61]. The pool of membrane PC could be a part of this regulation.
4. Not only proteins but also membrane lipid compartments are necessary for TNF-α signalling to occur. It has been previously shown that TNF-α binding recruits TNF-α-R1 to lipid rafts [
28]. Rafts are small platforms composed of sphingolipids and cholesterol in the outer exoplasmic leaflet and connected to phospholipids and cholesterol in the inner cytoplasmic leaflet of the lipid bilayer [
62]. These assemblies are fluid but more ordered and tightly packed than the surrounding bilayer. The difference in packing is due to the saturation of the hydrocarbon chains in raft sphingolipids and phospholipids as compared with the unsaturated state of fatty acids of phospholipids in the surrounding bilayer [
62]. Therefore it is possible that a change in the phospholipid concentration within the membrane has an impact on the lipid raft integrity. Discrepancies in the localisation of TNF-α-R1 to lipid rafts exist. Although in U937 and NIH-3T3 cells TNF-α-Rs were found mainly in lipid rafts and were shifted to detergent soluble parts upon TNF-α stimulation [
63], TNF-α increased their lipid raft association in HeLa [
64] and HT1080 fibrosarcoma cells [
65]. Conflicting data also exist concerning a compartmentalised NF-kB activation. Whereas some authors claim that NF-kB activation by TNF-α occurs in lipid raft domains [
28] other publications suggest a lipid-raft-independent activation [
63]. However, our data showed that upon exposure of Caco-2 cells with PC or LPC, the lipid raft associations of both TNF-α-R1 and TNF-α-R2 are increased and both lipids were inhibitory in our setting. Therefore, we assume that TNF-α-induced NF-kB activation occurs outside lipid rafts.
To get closer to the scenario in the mucosa, polarised Caco-2 cells were analysed as well. Although polarised cells could only be stimulated by basolateral exposure to TNF-α, an inhibitory effect of PC could be observed from both the apical and basolateral sides. The cause of this phenomenon requires further investigation; however, a possible explanation may be that TNF-α signalling occurs after internalisation and that apical and basolateral vesicles mix with each other in the endosomal compartments [
56]. Another possible explanation is that PC is integrated and rapidly exchanged between the apical and basolateral domains via the inner layer of the plasma membrane [
66].
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
RE precipitated in the design of the study and in the data analysis. He drafted the manuscript. AB, IT and PJ carried out the experiments. TG performed the RT-PCR analysis. JF, WS and GG were involved in the design of the study. All authors read and approved the final manuscript.