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J. Biol. Chem., Vol. 282, Issue 17, 13098-13113, April 27, 2007
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From the
¶Central Texas Veterans Health Care System and the Departments of Medicine and ||Systems Biology and Translational Medicine and Division of Research and Education, Scott and White Hospital and Texas A&M University System Health Science Center College of Medicine, Temple, Texas 76504
Received for publication, August 28, 2006 , and in revised form, February 26, 2007.
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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-cyclodextrin and filipin, we demonstrated that anandamide, but not 2-arachidonylglycerol, requires lipid raft-mediated events to inhibit cellular proliferation. Closer inspection of the lipid raft structures within the cell membrane revealed that although anandamide treatment had no observable effect 2-arachidonylglycerol treatment effectively dissipated the lipid raft structures and caused the lipid raft-associated proteins lyn and flotillin-1 to disperse into the surrounding membrane. In addition, anandamide, but not 2-arachidonylglycerol, induced an accumulation of ceramide, which was required for anandamide-induced suppression of cell growth. Finally we demonstrated that anandamide and ceramide treatment of cholangiocarcinoma cells recruited Fas and Fas ligand into the lipid rafts, subsequently activating death receptor pathways. These findings suggest that modulation of the endocannabinoid system may be a target for the development of possible therapeutic strategies for the treatment of this devastating cancer. |
INTRODUCTION |
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TOPABSTRACTINTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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Marijuana and its derivatives have been used in medicine for many centuries, and presently there is an emerging renaissance in the study of the therapeutic effects of cannabinoids. Ongoing research is determining that regulation of the endocannabinoid system may be effective in the treatment of pain (3, 4), glaucoma (5), and neurodegenerative disorders such as Parkinson disease (6) and multiple sclerosis (7). In addition, cannabinoids might be effective antitumoral agents because of their ability to inhibit the growth of various types of cancer cell lines in culture (8-11) and in laboratory animals (12).
The finding in the early 1990s of specific G-protein-coupled receptors for the psychoactive component of Cannabis sativa (-)-
9-tetrahydrocannabinol (13) led to the discovery of a whole endogenous signaling system now known as the endocannabinoid system (14). This system consists of the cannabinoid receptors (to date there are two, Cb12 and Cb2, as well as a putative involvement of the vanilloid receptor VR1), their endogenous ligands (endocannabinoids), and the proteins for their synthesis and inactivation (14). The cannabinoid receptors are seven-transmembrane domain proteins coupled to the Gi/o type of G-proteins (14). Cb1 receptors are found predominantly in the central nervous system but also in most peripheral tissues including immune cells, the reproductive system, the gastrointestinal tract, and the lung (15-17). On the other hand, Cb2 receptors are found predominantly in the immune system, i.e. in tonsils, spleen, macrophages, and lymphocytes (15-17). To date, many endocannabinoids have been identified with varying affinities for the receptors (18). Anandamide (AEA) was the first endogenous ligand to be identified (15); it acts as a partial Cb1 agonist and weak Cb2 agonist. Another endocannabinoid is 2-arachidonylglycerol (2-AG), which activates both Cb1 and Cb2 receptors (19, 20). The chemical structures of these two endocannabinoids are shown in Fig. 1. Although the physiological role of the many other ligands has not yet been fully clarified, AEA and 2-AG have been implicated in a wide variety of physiological and pathological processes.
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In the present study, we show the opposing effects of AEA and 2-AG on cholangiocarcinoma cell growth that were cannabinoid receptor-independent. In addition, we show that AEA mediated its inhibitory effects on cell growth by stimulating the accumulation of ceramide, stabilization of lipid rafts, and the recruitment of Fas and Fas ligand (FasL) to the lipid rafts. Conversely 2-AG increased cholangiocarcinoma cell growth and disrupted the organization of the lipid raft structures in the cell membrane.
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EXPERIMENTAL PROCEDURES |
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TOPABSTRACTINTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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Cell Culture—We used four human cholangiocarcinoma cell lines (Mz-ChA-1, HuH-28, HuCC-T1, and SG231) with different origins. Mz-ChA-1 cells, from human gallbladder (33), were a gift from Dr. G. Fitz (University of Texas Southwestern Medical Center, Dallas, TX). HuH-28 cells, from human intrahepatic bile duct (34), were acquired from Cancer Cell Repository, Tohoku University, Sendai, Japan. These cells were maintained at standard conditions as described previously (35). In addition HuCC-T1 (36) and SG231 cells (37), also from intrahepatic bile ducts, were a kind gift from Dr. A. J. Demetris (University of Pittsburgh, Pittsburgh, PA) and were cultured as described previously (36, 37). The human immortalized, nonmalignant cholangiocyte cell line H69 (from Dr. G. J Gores, Mayo Clinic) was cultured as described previously (38).
Reverse Transcription-PCR Analysis—We evaluated the expression of the cannabinoid receptors by reverse transcription-PCR using total RNA (1 µg) from H69, Mz-ChA-1, HuH-28, HUCC-T1, and SG231 cholangiocarcinoma cells. cDNA synthesis was performed using the Reaction ReadyTM first strand cDNA synthesis kit from SuperArray. For PCR, we used primers specific for human Cb1, Cb2, VR1, and glyceraldehyde-3-phosphate dehydrogenase (Cb1: forward, 5'-ctggttctgatcctggtggt-3'; reverse, 5'-tgtctcaggtccttgctcct-3'; product size, 185 bp; Cb2: forward, 5'-gattggcagcgtgactatga-3'; reverse, 5'-gctgagaggacccacatgat-3'; product size, 159 bp; VR1: forward, 5'-gcctggagctgttcaagttc-3'; reverse, 5'-tctcctgtgcgatcttgttg-3'; product size, 177 bp). PCR was performed using the following thermocycler conditions: 5 min at 94 °C followed by 30 cycles of 30 s at 94 °C, 30 s at 60 °C, and 45 s at 72 °C followed by a prolonged extension step for 5 min at 72 °C. Ten microliters of each PCR product were separated on a 1.5% agarose gel and stained with ethidium bromide and visualized using a ChemiImager low light imaging system (Alpha Innotech Corp., San Leandro, CA). Sequence analysis (Davis Sequencing, Davis, CA) indicated that the reverse transcription-PCR fragments for all cannabinoid receptors were homologous to their corresponding published sequence (GenBankTM accession numbers: human Cb1, AY995204 [GenBank] ; Cb2, NM_001841 [GenBank] ; and VR1, NM_080704 [GenBank] ).
Immunoblots—Following trypsinization, H69, Mz-ChA-1, HuCC-T1, SG231, and HuH-28 cells (1 x 106) were resuspended in lysis buffer as described previously (35, 39) and sonicated six times (30-s bursts). Immunoblots to detect Cb1, Cb2, and VR1 receptor expression were performed as described previously (35, 39).
Immunofluorescence—We detected Cb1, Cb2, and VR1 receptor expression in H69, Mz-ChA-1, HuCC-T1, HuH-28, and SG231 cells. Cells were seeded into 6-well dishes containing a sterile coverslip on the bottom of each well. Cells were allowed to adhere overnight, washed once in cold PBS, fixed to the coverslip with 4% paraformaldehyde (in 1x PBS) at room temperature for 5 min, permeabilized in PBS containing 0.2% Triton X-100 (PBST), and blocked in 4% bovine serum albumin (BSA) in PBST for 1 h. Cb1, Cb2, and VR1 receptor antibodies were diluted (1:50 for Cb1 and VR1 antibodies and 1:100 for Cb2) in 1% BSA in PBST, added to the coverslips, and incubated overnight at 4 °C. Cells were washed 3 x 10 min in PBST, and a 1:50 dilution (in 1% BSA in PBST) of Cy3-conjugated secondary antibodies (Jackson Immunochemicals, West Grove, PA) was added for 2 h at room temperature. Cells were washed again and mounted into microscope slides with Prolong Antifade Gold containing 4',6-diamidino-2-phenylindole (DAPI) as a counterstain (Molecular Probes, Eugene, OR). Negative controls were done with the omission of the respective primary antibodies. Sections were visualized using an Olympus IX-71 inverted confocal microscope.
Cell Proliferation Assays—Cholangiocarcinoma growth was evaluated by a 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxyme-thoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt (MTS) proliferation assay in the Mz-ChA-1, HuCC-T1, HuH-28, and SG231 cell lines (40). After trypsinization, cells were seeded into 96-well plates (10,000 cells/well) in a final volume of 200 µl of medium. Cells were stimulated for 24, 48, and 72 h with AEA or 2-AG (1 nM to 10 µM). Cell proliferation was assessed using a colorimetric cell proliferation assay (CellTiter 96Aqueous, Promega Corp., Madison, WI), and absorbance was measured at 490 nm by a microplate spectrophotometer (Versamax, Molecular Devices, Sunnyvale, CA).
To determine possible mechanisms of action, Mz-ChA-1 cells were first preincubated for 1 h with various inhibitors prior to the addition of AEA or 2-AG for 48 h. The inhibitors utilized were SR141716 (a Cb1 antagonist, 10 nM (41)); SR144528 (a Cb2 antagonist, 10 nM) (42); AMG9810 (a VR1 antagonist, 10 nM (43)); pertussis toxin (Gi/o protein inhibitor, 100 ng/ml (44)); methyl--cyclodextrin (0.1 mM), which depletes intracellular cholesterol and hence disrupts lipid rafts (45); filipin III (1 µg/ml), which binds and cross-links intracellular cholesterol and hence disrupts lipid rafts (46, 47); L-cycloserine (0.5 mM), a de novo ceramide synthesis inhibitor (48); or spiroepoxide (100 nM), which inhibits ceramide synthesis by hydrolysis of sphin-gomyelin (49).
In all cases, data were expressed as the -fold change of treated cells as compared with vehicle-treated controls. Statistical significance was determined using a t test, and p < 0.05 was considered significant.
Annexin V Labeling—Apoptosis was evaluated using Annexin V labeling of cells (50). Mz-ChA-1 cells were seeded in 6-well plates (500,000 cells/well) containing sterile coverslips on the bottom of each well and allowed to adhere overnight. Cells were stimulated with AEA (10 µM) or 2-AG (10 µM) for 24 h after which time coverslips were removed and rinsed in cold incubation buffer (10 mM HEPES, pH 7.4, 140 mM NaCl, 5 mM CaCl2) to remove excess media. Coverslips were then incubated in a solution containing Annexin V-biotin complex (1:50 dilution in incubation buffer) for 30 min at room temperature. After washing the coverslips to remove excess Annexin V-biotin, the cells were fixed in cold 4% paraformaldehyde (in PBS) for 10 min. Bound Annexin V-biotin complex was detected with Cy2-labeled streptavidin (1:200 dilution in PBS), mounted onto microscope slides with Prolong Antifade Gold containing DAPI, and visualized using an Olympus IX-71 inverted confocal microscope. The number of Annexin V-positive cells was counted and expressed as a percentage of total cells in five random fields for each treatment group. Data are the average ± S.E. of five fields in three independent experiments.
BrdUrd Labeling—BrdUrd labeling was used to evaluate the effects of AEA and 2-AG on cell cycle progression. Mz-ChA-1 cells were seeded in 6-well plates (500,000 cells/well) containing sterile coverslips on the bottom of each well and allowed to adhere overnight. Cells were stimulated with AEA (10 µM) or 2-AG (10 µM) for 48 h after which time BrdUrd (10 µM final concentration) was added to each well and incubated for a further 3 h at 37 °C. The coverslips were removed, rinsed in PBS to remove excess media, and fixed in 4% paraformaldehyde (in PBS) for 10 min at room temperature. DNA was denatured in 2 M HCl for 1 h at 37 °C and then neutralized with 0.5 M borate buffer (pH 9.5). The cell membranes were then permeabilized with PBST for 3 x 5 min. Nonspecific protein binding was then blocked with 4% BSA (in PBST) for 1 h at room temperature followed by a 2-h incubation with a 1:200 dilution (in 1% BSA in PBST) of anti-BrdUrd antibody. Coverslips were washed 3 x 5 min in PBST, and a 1:50 dilution (in 1% BSA in PBST) of Cy3-labeled anti-mouse secondary antibody was added and incubated for 2 h at room temperature. Excess antibody was removed by further washing in PBST, and the coverslips were mounted onto microscope slides with Prolong Antifade Gold containing DAPI and visualized using an Olympus IX-71 inverted confocal microscope. The number of BrdUrd-positive nuclei was counted and expressed as a percentage of total cells in five random fields for each treatment group. Data are the average ± S.E. of five fields in three independent experiments.
Lipid Raft Labeling—Lipid rafts were visualized using the Vybrant® lipid raft labeling kit (Molecular Probes) with modifications. Briefly Mz-ChA-1 cells were seeded onto sterile coverslips placed in the bottom of 6-well culture dishes and allowed to adhere overnight. Cells were treated with vehicle, AEA, or 2-AG (both at 10 µM) for 4 h at 37 °C. Coverslips were then moved into new 6-well dishes for staining. Cells were incubated in the presence of 1 µg/ml (diluted in growth media) of fluorescent cholera toxin B subunit (Alexa Fluor 594 was the fluorochrome) for 15 min at 4 °C. This cholera toxin B subunit conjugate binds to the pentasaccharide chain of plasma membrane ganglioside GM1, which selectively partitions into lipid rafts (51, 52). After this incubation, the cells were gently washed with chilled PBS, fixed in 4% paraformaldehyde (in PBS) for 15 min at 4 °C, washed again in PBS, mounted onto microscope slides with Prolong Antifade Gold containing DAPI, and visualized using an Olympus IX-71 inverted confocal microscope. In the lipid raft/Fas co-localization studies, the lipid rafts were stained and fixed in 4% paraformaldehyde as described above. The cells were then counterstained with an antibody against the extracellular domain of Fas overnight at 4 °C under non-permeabilizing conditions (i.e. all washes were performed in PBS instead of PBST). Immunofluorescent staining of membranebound Fas was continued as described above using a Cy2-labeled anti-rabbit secondary antibody. Analysis of the degree of co-localization between lipid rafts and Fas immunoreactivity was performed using a Pearson's correlation analysis that is part of the FluoView imaging software from Olympus. Using this analysis, complete co-localization of the two stains is represented by a Pearson's coefficient of 1.0, whereas complete non-colocalization gives a Pearson's coefficient of -1.0.
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-tubulin, flotillin-1, Fas, and FasL or -actin. Cholesterol Assays—Cholesterol content was determined in total cell extracts as well as in each of the lipid raft fractions (50-µl sample volume) after basal, AEA (10 µM), and 2-AG (10 µM) treatment using the cholesterol determination kit from Molecular Probes according to the manufacturer's instructions. For total cholesterol content, results were corrected for protein content in each sample and expressed as average ± S.E. in three samples. For the cholesterol content in lipid raft fractions, results were expressed as the average (±S.E.) of the percentage of the total cholesterol content in three samples.
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Sphingomyelinase Assays—Sphingomyelinase activity was determined in samples 1, 2, and 4 h after AEA (10 µM) treatment using the sphingomyelinase assay kit purchased from Molecular Probes according to the instructions supplied by the vendor. This assay was performed under neutral and acidic conditions to assess both neutral and acidic sphingomyelinase activity. Data were expressed as -fold change in activity of four samples (average ± S.E.).
Transient Transfection—Mz-ChA-1 cells were seeded into 96-well plates (5,000 cells/well) and allowed to adhere overnight. Expression vectors containing dominant negative FADD or the control vector was transfected into the cells (0.1 µg of DNA/well) with 0.28 µl/well TransIT-LT1 transfection reagent (Mirus, Madison, WI) overnight at 37 °C. The cells were then incubated under basal conditions or stimulated with AEA (10 µM) for 48 h, and cell viability was determined by MTS assay as described above.
In addition, FADD expression was knocked down using shRNA plasmids containing a green fluorescent protein label from SuperArray. Four plasmids containing shRNA sequences against different regions of the human FADD gene were tested. Mz-ChA-1 cells were plated into 96-well plates and transiently transfected with the shRNA plasmids as described above. Transfection efficiency was monitored using fluorescence microscopy and determined to be equal in every well and at an efficiency of 
60%. MTS assays were then performed as described above. In a parallel experiment Mz-ChA-1 cells were seeded into 6-well plates and transfected with the shRNA plasmids. After 48 h, RNA was extracted as described above, and FADD expression was determined by real time PCR. Briefly reverse transcription was performed using the Reaction Ready first strand cDNA synthesis kit (SuperArray). The real time PCRs were set up in 96-well plates using the SYBR Green PCR Master Mix kit (SuperArray) and either specific primers for human FADD or glyceraldehyde-3-phosphate dehydrogenase (SuperArray). The fluorescence was monitored continuously throughout 40 cycles of amplification (95 °C for 15 s and 60 °C for 1 min) using the ABI Prism 7900HT sequence detection system. A CT analysis was performed, and data were expressed as -fold change of FADD mRNA expression after correction for glyceraldehyde-3-phosphate dehydrogenase expression.
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RESULTS |
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TOPABSTRACTINTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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Effect of Endocannabinoids on Cholangiocarcinoma Cell Growth—MTS proliferation assays revealed that AEA (10 µM) significantly decreased cell growth 48 h after stimulation (Fig. 3A) and up to 72 h (data not shown) in all cholangiocarcinoma cell lines studied. This concentration far exceeded the Ki values for any of the cannabinoid receptors (Ki = 89 and 371 nM at Cb1 and Cb2, respectively (56, 57)). Concentrations below 10 µM had no effect on growth. In contrast, the other most abundant endocannabinoid, 2-AG (10 µM), had a stimulatory effect on cholangiocarcinoma cell growth at 48 h (Fig. 3B) and 72 h (data not shown). Once again, there was no effect at concentrations below 10 µM. The fact that these endocannabinoid-induced effects on cell growth were seen at concentrations that far exceed the binding affinities for any of the cannabinoid receptors suggests that these effects are probably receptor-independent. Indeed specific cannabinoid antagonists failed to block the AEA- and 2-AG mediated effects (Fig. 4, A and B). In addition, because these cannabinoid receptors are coupled to Gi/o proteins, we used pertussis toxin, an inhibitor of these proteins (44), to determine whether AEA or 2-AG is functioning through a Gi/o protein-coupled receptor. As seen in Fig. 4, A and B, pertussis toxin failed to inhibit either AEA-mediated inhibition or 2-AG stimulation of cholangiocarcinoma cell growth. These inhibitors, however, did effectively block the AEA-mediated suppression of forskolin-induced cAMP production in these cells (data not shown) in a manner similar to that in previous studies (58-60), indicating that the receptor antagonists are indeed functional at the concentrations used here. This indicates that neither endocannabinoid is exerting its effects through the cannabinoid receptors or any other Gi/o-coupled receptor.
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27% of the cholangiocarcinoma cells stained positive for Annexin-V under the basal conditions of our experiment. This value increased up to 60% after AEA treatment for 48 h, whereas 2-AG treatment decreased the incidence of apoptosis slightly but significantly down to 20% Annexin V-positive cells.
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40% of the cells took up BrdUrd into their DNA under the control conditions of these experiments (Fig. 5B). AEA treatment, however, decreased the amount of BrdUrd-positive cells and hence the rate of cell cycle progression, and 2-AG treatment increased the rate of cell cycle progression.
Endocannabinoids Exert Their Effects through Cholesterol-rich Lipid Rafts—Cannabinoids have been shown previously to have receptor-independent effects through interaction with lipid rafts (21-23). Therefore, we evaluated whether the receptor-independent effects of AEA and 2-AG shown here are also mediated through lipid rafts. Treatment of Mz-ChA-1 cells with the lipid raft disrupter methyl--cyclodextrin (45) had no effect on basal proliferation (Fig. 6A). However, pretreatment with methyl--cyclodextrin inhibited the AEA-mediated suppression of cell proliferation but failed to prevent the 2-AG-induced stimulation of proliferation (Fig. 6A). Similar results were observed following treatment of Mz-ChA-1 cells with filipin III, which disrupts lipid raft structure by a mechanism different from that of methyl--cyclodextrin (46) (Fig. 6B). Taken together these data suggest that AEA requires the integrity of the lipid raft membrane structure to be intact to induce the signal transduction pathways that ultimately result in increased apoptosis/cell cycle inhibition, whereas this membrane structure is not required for 2-AG-mediated increase in proliferation.
We then evaluated the effects of both AEA and 2-AG on the integrity of the lipid raft membrane structures by staining the GM1 gangliosides, which are an integral component of lipid rafts (51, 52). Fig. 7A, shows the lipid raft structures on the membranes of Mz-ChA-1 cells under basal conditions. The distribution and morphology of these lipid rafts did not appear to change significantly after AEA treatment. Stimulation of the cells with 2-AG, however, resulted in marked changes in the lipid raft staining patterns (Fig. 7A). The staining became more diffuse and apparently less membranous suggesting that perhaps 2-AG effectively disrupts the lipid raft structure and hence any lipid raft-mediated control of the intracellular machinery responsible for the initiation of apoptosis and/or cell cycle progression. To further demonstrate this phenomenon, we isolated the detergent-resistant membrane fractions on an OptiPrep density gradient. Previous studies have shown that using a similar method the lipid rafts migrate to the interface between the 5 and 30% OptiPrep layers (61). Under the conditions used in the experiments outlined here, this corresponds to fractions 3 and 4. Using lyn and flotillin-1 as lipid raft markers, it can be seen that the lipid rafts did indeed migrate to the interface between the 5 and 30% OptiPrep layers under both basal conditions and after AEA treatment (i.e. lyn and flotillin-1 were found predominantly in fractions 3 and 4, Fig. 7B). However, 2-AG treatment resulted in the detection of lyn and flotillin-1 in many other fractions besides fractions 3 and 4 (Fig. 7B) suggesting that the integrity of the lipid rafts was compromised and that components that are usually found exclusively in the raft fraction diffused into the surrounding membrane. In these experiments, the non-raft-associated -tubulin was used as a negative control to show that under our experimental conditions not all proteins are found in fractions 3 and 4 and that 2-AG does not disrupt the intracellular organization of all proteins (Fig. 7B).
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AEA, but Not 2-AG, Increases Intracellular Ceramide Levels—AEA has been shown previously to increase ceramide levels within the cell (24), and ceramide is an integral component of the lipid raft-mediated signaling cascade (62). For this reason we determined the effects of AEA and 2-AG on intracellular ceramide levels using a specific antibody. As can be seen in Fig. 9A, AEA increased the intracellular ceramide levels 2-fold from basal conditions, whereas 2-AG had no effects. Furthermore both the acid and neutral sphingomyelinase activities were significantly induced from 1 to 4 h after AEA treatment (Fig. 9B). By treating Mz-ChA-1 cells with various concentrations of C2- and C6-ceramide, we showed that ceramide causes a decrease in cell proliferation similar to that seen after AEA treatment as shown by MTS assay (Fig. 9C). In addition, pretreatment of the cells with spiroepoxide and L-cycloserine, inhibitors of the two pathways leading to the accumulation of ceramide, resulted in an inhibition of the AEA-mediated suppression of cell growth but no effect on the 2-AG-mediated enhancement of cell growth (Fig. 9D). Taken together, these data suggest that AEA, but not 2-AG, causes an increase in intracellular ceramide and that this ceramide accumulation is essential for the decrease in cellular proliferation seen after AEA treatment.
Involvement of Fas Activation in AEA-mediated Proapoptotic Pathway—Because AEA appears to activate proapoptotic events in cholangiocarcinoma cell lines, we wanted to determine what involvement the death receptor complexes of the TNF superfamily has in this pathway. These death receptors are all capable of using FADD as a downstream effector molecule (63-65). Therefore, we transiently transfected a dnFADD expression vector into the Mz-ChA-1 cells to determine whether blocking the death receptor cascade has any effect on the AEA-induced cell death. Indeed transient dnFADD expression significantly inhibited the AEA-mediated suppression of cell growth as shown by MTS assay (Fig. 10A). In a similar experiment, we used shRNA vectors to knock down FADD expression. Transient transfection of the four different vectors knocked down the expression of FADD to 25-60% of the expression levels after transfection of the empty vector (Fig. 10B). This specific gene knockdown was enough to block the antiproliferative effects of AEA on Mz-ChA-1 cells. Total blockage of this antiproliferative effect by either dnFADD or the shRNA vectors was not achieved because the transfection efficiency was only 50-60%.
In addition, using the lipid raft plasma membrane fractions, we showed that under basal conditions Fas and FasL were predominantly found in fractions 6 and 7, i.e. the non-lipid raft-containing fractions (Fig. 10C). Upon AEA stimulation these receptor components could also be detected in the lipid raft fractions (fractions 3 and 4; Fig. 10C), which presumably facilitates in the death receptor complex formation and subsequent activation of proapoptotic pathways. In addition, the recruitment of Fas and FasL into the lipid raft fractions was also observed after C6-ceramide treatment (Fig. 10C) suggesting that the accumulation of ceramide may indeed be responsible for the effects of AEA on lipid raft proteins. Furthermore pretreatment with the ceramide synthesis inhibitor spiroepoxide prior to the addition of AEA blocked the recruitment of both Fas and FasL into the lipid raft fractions.
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DISCUSSION |
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TOPABSTRACTINTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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Consistent with our observation that AEA has antiproliferative and proapoptotic properties, cannabinoids of various origins (endogenous, plant-derived, or synthetic analogues) have been shown to suppress cancer cell growth in vitro (8-11) as well as in vivo (12). Indeed recently a clinical pilot study to determine the safety of intracranial administration of (-)-9-tetrahydrocannabinol in patients with glioblastoma demonstrated a marked reduction in Ki67 staining within the tumor (66). This observation together with the very promising results observed in cell cultures and laboratory animals (8-12) suggest that administering cannabinoids alone or in conjunction with existing chemotherapeutic agents may be a promising treatment strategy for aggressive cancers of various origins. Another strategy may be to administer drugs that inhibit endocannabinoid uptake and subsequent degradation. Bifulco et al. (67) showed that administration of inhibitors of endocannabinoid cellular reuptake and endocannabinoid enzymatic hydrolysis into athymic mice with thyroid tumor xenografts effectively enhanced the endocannabinoid concentrations within the tumor and suppressed the tumor growth. In the present study, we also observed that, in contrast to AEA, 2-AG treatment resulted in an increase in cholangiocarcinoma cell growth. Although growth-promoting effects of cannabinoids in tumors of various origins have been demonstrated previously (26), to our knowledge, this is the first demonstration of the opposing effects of these two endocannabinoids within the one tumor type. To date, 2-AG is the only cannabinoid assayed that has this growth-promoting effect in cholangiocarcinoma cells.3 In light of this, as well as the fact that 2-AG is the most abundant endocannabinoid in tissues (14), caution must be taken when developing a chemotherapeutic strategy that results in an "across the board" increase in endocannabinoid levels. A treatment that specifically targets AEA levels without effecting 2-AG levels would obviously be preferable for this tumor type.
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In our studies, we demonstrated that 1) AEA induced an accumulation of ceramide within the cell, and 2) this ceramide accumulation was essential for the subsequent AEA-induced cell death. Ceramide is an integral component of the lipid raft structure and dramatically changes the biophysical properties of the rafts, allowing very tight packing of lipids within the rafts (72) and hence strongly stabilizing this membrane structure (73). This then facilitates the clustering or aggregation of various receptor molecules (74), which may theoretically have several functions including bringing many receptor molecules in close proximity to facilitate the transactivation between different receptor systems (74). It may also enhance the interaction between a receptor and its intracellular signaling molecules (75). In addition, raft ceramide may directly activate signal transduction pathways such as the Raf-1/MEK/ERK pathway (12, 76). The ceramide accumulation seen here after AEA treatment, we believe, is functioning to stabilize the lipid raft structure; however, the direct effect of ceramide on signal transduction pathways ultimately resulting in cell death cannot be ruled out and is a subject of our ongoing research. Indeed the tumor necrosis factor receptor molecule contains activator domains capable of inducing ceramide production by the activation of sphingomyelinase (77, 78), and this is FADD-dependent (79). Therefore it is also possible that instead of the AEA-induced accumulation of ceramide resulting in the stabilization of lipid rafts and recruitment of death receptors, AEA may first recruit the death receptor complex, which then results in the accumulation of ceramide. Regardless of the sequence of events, our data demonstrate a requirement for ceramide synthesis in the antiproliferative effects of AEA. The precise role of this phenomenon will be dissected further in our laboratory.
Data, such as those presented here, demonstrating the recruitment of protein components of the death receptor complexes into lipid raft structures are voluminous. It is widely accepted that both the TNF-receptor complex and the Fasreceptor complex are both recruited into lipid rafts in response to apoptosis-inducing drugs; this recruitment facilitates the receptor complex formation and is critical for their function (80-82). However, the stimulation of this recruitment into lipid rafts by cannabinoids has not been demonstrated previously in any cell type. In addition, these receptor complexes all require FADD to function (65). By overexpressing dominant negative FADD, we blocked the antiproliferative effects of AEA, suggesting that the formation of these death receptor complexes is required for the AEA-mediated effects on cholangiocarcinoma cell growth.
The effects of death receptor activation on cholangiocarcinoma cell growth have been demonstrated previously (83, 84). Tanaka et al. (83) showed that although the expression of TNF-related apoptosis-inducing ligand receptors (including DR4 and DR5) is not changed between resected cholangiocarcinoma samples and the surrounding normal liver tissue, exposure of cholangiocarcinoma cells to TNF-related apoptosis-inducing ligand (ligand of DR5) increased the incidence of apoptosis in vitro and in vivo and reduced the volume of a subcutaneous xenograft of human cholangiocarcinoma cells in vivo. In addition, Fas expression has been shown to negatively regulate cholangiocarcinoma cell growth in a xenograft model (84). Taken together, we propose that AEA facilitates the activation of these receptor complexes, in particular the Fas receptor, by their recruitment into lipid rafts, resulting in a proapoptotic phenomenon.
In conclusion, we have clearly demonstrated opposing actions of the endocannabinoids AEA and 2-AG on cholangiocarcinoma cell proliferation and have shown that these actions are via a cannabinoid receptor-independent but lipid raft-mediated pathway. Furthermore we have shown that the antiproliferative/proapoptotic actions of AEA are mediated via an accumulation of ceramide and the recruitment of the Fas death receptor into the lipid rafts. Cholangiocarcinoma has a very poor prognosis and survival rate; therefore we propose that the development of novel therapeutic strategies aimed at modulating the endocannabinoid system or mimicking the mode of action of AEA would prove beneficial for the treatment of this devastating disease.
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FOOTNOTES |
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1 To whom correspondence should be addressed: Depts. of Medicine and Systems Biology and Translational Medicine, Central Texas Veterans Health Care System, Texas A&M University System Health Science Center College of Medicine, Medical Research Bldg., 702 S. W. H. K. Dodgen Loop, Temple, TX 76504. Tel.: 254-742-7044; Fax: 254-724-8070; E-mail: galpini{at}tamu.edu.
2 The abbreviations used are: Cb1, cannabinoid receptor 1; Cb2, cannabinoid receptor 2; 2-AG, 2-arachidonylglycerol; AEA, anandamide; BrdUrd, bro-modeoxyuridine; DAPI, 4',6-diamidino-2-phenylindole; dnFADD, dominant negative FADD; DR, death receptor; FADD, Fas-associated death domain protein; MTS, 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt; PBS, phosphate-buffered saline; TNF, tumor necrosis factor; VR1, vanilloid receptor; FasL, Fas ligand; MES, 4-morpholineethanesulfonic acid; shRNA, short hairpin RNA; BSA, bovine serum albumin; MEK, mitogen-activated protein kinase/extracellular signal-regulated kinase kinase; ERK, extracellular signal-regulated kinase.
3 S. DeMorrow and G. Alpini, unpublished observation.
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TOPABSTRACTINTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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