Effects on inflammatory responses by the sphingoid base 4,8-sphingadienine
- Authors:
- Published online on: June 15, 2012 https://doi.org/10.3892/ijmm.2012.1035
- Pages: 703-707
Abstract
Introduction
Sphingolipids (SLs) are a class of lipids, which are structural cell components involved in the regulation of cellular processes such as cell proliferation, differentiation, apoptosis and inflammation (1–5). The basic structure of SLs contains a sphingoid base that is N-acylated with a fatty acid and C-1 linked to a polar head group. SLs are found in eukaryotes and prokaryotes and are well studied in mammals (6). The mammalian SL metabolites ceramide, sphingosine and sphingosine 1-phosphate have drawn attention as bioactive signaling molecules.
Inflammation is important in the healing processes of tissue injury or infections. Tumor necrosis factor-α (TNF-α) and lipopolysaccharide (LPS) are essential pro-inflammatory stimuli involved in the pathogenesis of chronic inflammatory diseases. Chronic inflammation, however, is harmful to tissue and is considered to underlie the onset and development of a wide variety of pathological responses causing tissue damage. Diseases such as cancer, atherosclerosis, insulin resistance and diabetes are associated with chronic inflammation (7). Therefore the timely shut down of inflammatory processes is of utmost importance to maintain individual health.
Dietary SLs, such as glucocerebrosides (GluCer) derived from plants, are enzymatically hydrolyzed by brush border enzymes in the gut lumen into metabolites namely ceramides and sphingoid bases. This results in the uptake of the derived ceramides and sphingoid bases by intestinal epithelial cells (8–10). Sphingoid bases or ‘sphingosines’ occur in a great variety in type and chain length, such as sphingosine (d18:1) in mammals, and sphingomyelin (d16:1) in milk (11,12). Several studies have reported on SLs regulating inflammatory responses at multiple levels (4,13).
Research of anti-inflammatory effects of plant GluCer and sphingoid bases is very limited. 4,8-Sphingadienine (4,8-SD) (d18:2) is the sphingoid backbone of the characteristic GluCer present in the Araceae species Arisaema amurense Maxim. (14) and Pinellia ternata (Thunb.) Breit., as well as in plants in human diet such as spinach, soybean and eggplant (11,15).
To the best of our knowledge, this is the first time the effect of the plant-derived sphingoid base on inflammatory responses was tested by investigation of the regulation of TNF-α- and LPS-induced expression of IL-8 and E-selectin.
Materials and methods
Materials
Fetal calf serum (FCS) was purchased from HyClone (Logan, UT, USA) and TNF-α was from Genzyme (Cambridge, MA, USA). BAY 11–7085 (BAY) (purity ≥98%), medium 199, o-phenylenediamine and LPS from E. coli serotype 055:B5 were purchased from Sigma-Aldrich (Vienna, Austria). The 4,8-SD obtained after hydrolysis of GluCer was isolated from Arisaema amurense Maxim. (Araceae) and purified by silica column chromatography (CC). Polyclonal antibodies were purchased from R&D Systems (Minneapolis, MN, USA) and peroxidase-conjugated secondary antibodies from Amersham Life Science (Amersham, UK). For extraction, fractionation and isolation by CC solvents of highest available purity were used (VWR, Vienna, Austria). All other chemicals were obtained from Sigma-Aldrich.
Plant material
Dried, processed rhizomes of Arisaema amurense Maxim. were purchased from Plantasia (Oberndorf, Austria). A voucher specimen, encoded ER-I, was deposited at the Department of Pharmacognosy, University of Vienna.
Isolation of GluCer and 4,8-SD
The dried, processed rhizomes of A. amurense (1.9 kg) were pulverized and extracted by dichloromethane and subsequently 1.4 kg of this material was extracted with methanol. The dried extracts were chromatographed over a silica column eluted by CHCl3:MeOH:H2O 98:2:1 to 60:38:8.5 to obtain fractions D1–8 for the dichloromethane extract (9.8 g) and eluted by CHCl3:MeOH:H2O 70:22:3.5 to 60:40:10 for the methanol extract (10.7 g) to obtain fractions M1–15. GluCer were isolated from fractions D8 (3.6 g) and M1 (2.5 g) by RP C-18 CC with methanol as mobile phase and subsequent silica CC with CHCl3:MeOH:H2O (65:25:4) as mobile phase (Fig. 1). A mixture of GluCer (40 mg) was hydrolyzed in methanolic 1 M HCl for 7 h at 70˚C under reflux. The hydrolyzed sample was neutralized and evaporated to dryness. The liberated sphin-goid base was purified by silica CC with CHCl3:MeOH:NH4 (40:10:1) as mobile phase (Fig. 2), with a yield of 5.5 mg.
GC-MS and NMR analysis
The pure compound was further converted to the N-acetyl-di-O-trimethylsilyl derivative and analyzed by GC-MS and NMR and identified as 4,8-sphingadienine (4,8-SD) (Fig. 3). The amide group was N-acetylated with acetic anhydride:MeOH (v/v 1:4) overnight at 25˚C. The sample was brought to dryness and further derivatized by BSTFA and TMCS (v/v 99:1) and incubated at 50˚C for 30 min. The analyses were performed on an Agilent Technologies 6890N Network GC equipped with an Agilent Technologies 5973 inert Mass selective Detector and a CombiPAL autosampler (CTC Analytics). The column used was a DB-5 with dimensions of 30 m x 0.25 mm (inner diameter), 0.23 μm (film thickness) (Agilent Technologies). The software used was MSD Chemstation 2004.
NMR spectra were recorded on a Bruker Avance 500 NMR spectrometer. 4,8-SD was dissolved in CDCl3 (99.96 atom % D). The 1H and 13C NMR spectra were operated at 500 and 125 MHz, respectively. The compound has a purity of at least 95% judging from the NMR-spectra.
4,8-SD was a brownish, yellow, amorphous solid. Electron impact mass spectrometry (EIMS) of the N-acetyl-di-O-trimethylsilyl derivative showed ions at m/z 73, 174, 309, 334, 378, 468 (16). For biological testing 4,8-SD was dissolved in DMSO.
Cells
The study was performed using immortalized human umbilical vein endothelial (HUVECtert) cells (17). In contrast to primary HUVECs, HUVECtert have the advantage of an indefinite cell division potential. However, the tert transfection alters the cells’ gene expression profile (18) affective the response to the dual treatment. HUVECtert were cultured in M199 medium supplemented with endothelial cell growth supplement (Technoclone), heparin, penicillin/streptomycin and 20% FCS. The cells were grown in a humidified atmosphere at 37˚C and 5% CO2 and passaged twice a week using trypsin-EDTA solution. Experiments were performed using cells up to passage 5.
Cell ELISA
HUVECtert cells (1x105 cells/well) were seeded in a 96-well plate and grown for 24 h overnight in a cell culture incubator. Monolayers of the grown HUVECtert cells were then treated with 4,8-SD or GluCer and agonists in medium 199 containing 5% FCS. 4,8-SD (0–45 μM) or BAY 11–7082 (5 μM), which served as positive control, were added to the cells 20 min before the addition of TNF (100 ng/ml) or LPS (100 ng/ml). BAY 11-7085 is an anti-inflammatory agent acting by inhibiting NF-κB thus decreasing expression of inflammatory molecules including E-selectin and IL-8 (19). The solvent vehicle (0.2% DMSO) served as the negative control. After 6 h, the medium was collected for quantification of IL-8, and the cells were washed and fixed with 4% glutaraldehyde for determination of E-selectin. Cell surface-expressed E-selectin was detected using corresponding antibodies, secondary peroxidase-conjugated antibodies and o-phenylenediamine as substrate essentially as described before (20). Concentrations of IL-8 in cell culture medium were determined using human CXCL8/IL-8 ELISA DuoSet ELISA Development kit (R&D Systems) and the TMB 2-Component Microwell Peroxidase Substrate kit (VWR International, Radnor, PA, USA). The absorbance was measured at 490 nm.
Cell proliferation/viability assays
The HUVECtert cells (1x105 cells/well) were seeded in 96-well plates. After 24 h test compounds (4,8-SD or GluCer) or vehicle (DMSO) were added. Cell viability and metabolic activity were assessed after 6 h either by the LDH (Sigma Aldrich, St. Louis, MO, USA) or WST-1 (Roche Applied Science, Mannheim, Germany) colorimetric assays. The absorbance was measured at 340 nm after 55 min for the LDH assay at 450 nm for the WST1-assay.
Data and statistical analysis
Statistical analysis and calculation of IC50 values were performed using the Prism Software (ver. 4.03; GraphPad Software Inc., San Diego, CA, USA). Data were normalized to the mean value from three experiments of DMSO treated control. The data shown represent the mean values out of at least three experiments ± SEM. Statistical significance was determined by a one-way analysis of variance combined with a Dunnett’s multiple comparison post test. Results with P<0.05 were considered significant.
Results
In our studies 4,8-SD (Fig. 3) blocked TNF-α- (Fig. 4) and LPS-induced (Fig. 5) upregulation of the inflammatory adhesion molecule E-selectin and the cytokine IL-8 in HUVECtert cells. 4,8-SD showed this inhibitory effect in a concentration-dependent manner. Half-maximal inhibition of TNF-α-induced upregulation of IL-8 (Fig. 4B) and E-selectin (Fig. 4C) was observed at 15.4 and 6.8 µM 4,8-SD, respectively. Half-maximal inhibition of LPS-induced upregulation of IL-8 (Fig. 5B) and E-selectin (Fig. 5C) was observed at 6.0 and 4.2 μM 4,8-SD, respectively. 4,8-SD exerted an inflammatory response by the unstimulated HUVECtert cells at the cytotoxic concentration of 30 μM, which exceeds the control (Figs. 4A and 5A).
In addition, it was investigated whether the treatment of the cells with 4,8-SD induced cell death that could influence TNF-α- and LPS-induced IL-8 and E-selectin expression. To this end, cytotoxic effects of 4,8-SD towards HUVECtert cells were investigated using the LDH and the WST-1 colorimetric assays. The viability of the cells decreased at concentrations greater than 20 μM 4,8-SD after 6 h of treatment (Fig. 6). In contrast to 4,8-SD, GluCer were poorly soluble in DMSO and lacked activity in both the ELISA and cell viability studies (data not shown).
Discussion
We observed that the sphingoid base 4,8-SD of GluCer from A. amurense inhibits the inflammatory responses induced by TNF-α and LPS in HUVECtert cells. The anti-inflammatory effects were observed at significantly lower concentrations of 4,8-SD compared to the cytotoxic effects. The GluCer however lacked effects on the HUVECtert cells in the presented in vitro bioassays. These findings confirm that GluCer may be metabolized to 4,8-SD in the gut lumen by enzymes in order to acquire cytotoxic and/or anti-inflammatory properties (5). The daily intake by humans of total SLs from plant sources is estimated to be as little as 50 mg (9,15). It is unknown what portion of 4,8-SD becomes bioavailable in the mucosal cells of the intestines after ingestion of complex SLs. However, it was reported that sphingadienines in general have the advantage over other SLs of being slowly metabolized and of having a long half-life in intestinal epithelial cells (21).
Previously, pro-apoptotic effects of 4,8-SD and various other sphingoid bases were reported which were regulated by activation of caspases thereby explaining the cytotoxic effects (22–25). Although there appears to be a difference between concentrations inhibiting IL-8 and E-selectin production and cytotoxicity, the effects induced by TNF-α and LPS could still be toxic to the cells. Therefore, deeper in vitro and in vivo studies regarding the anti-inflammatory and cytotoxic effects of 4,8-SD are required. Studies on the effect of 4,8-SD on a wider spectrum of pro- (e.g. IL-1β, IL-6, IL-12, IFNγ) and anti-inflammatory cytokines and mediators (e.g. IL-4, IL-10, IL-13), will provide insight in the compounds’ specificity and sensitivity. Furthermore, the effects of long-term exposure by 4,8-SD on its anti-inflammatory and cytotoxic activities and studies pertaining to the involved molecular mechanisms of this compound are needed.
Taken together, the present findings revealed that 4,8-SD alters the inflammatory responses of endothelial cells in vitro in a favorable way. Since the source of 4,8-SD can be found in the human diet, consecutive studies on the nutritional and therapeutical function of 4,8-SD merit attention.
Acknowledgements
This study was supported by the Sino-Austrian Research Project (to B.K.) funded by the Austrian Federal Ministry of Science and Research and Federal Ministry of Health, Women and Youth, and NFN-project ‘Drugs from Nature Targeting Inflammation - DNTI’, Subproject S10713 from the Austrian Science Fund (to V.B.).
Abbreviations:
CC |
column chromatography; |
CD |
circular dichromism; |
ELISA |
enzyme-linked immunosorbent assay; |
FCS |
fetal calf serum; |
GC-MS |
gas chromatography mass spectrometry; |
GluCer |
glucocerebrosides; |
IL-8 |
interleukin 8; |
LPS |
lipopolysaccharide; |
NMR |
nuclear magnetic resonance; |
4,8-SD |
4,8-sphingadienine; |
SL |
sphingolipid; |
TNF-α |
tumor necrosis factor-α |