|
|||||||||
|
|
|
|
|
|
|
|
|
|
|
Blood, 15 August 2005, Vol. 106, No. 4, pp. 1346-1354. Prepublished online as a Blood First Edition Paper on April 28, 2005; DOI 10.1182/blood-2004-04-1322.
NEOPLASIA Ectopic and IFN-induced expression of Fas overcomes resistance to Fas-mediated apoptosis in multiple myeloma cellsFrom the Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden; and Department of Hematology and Oncology, Karolinska Hospital, Stockholm, Sweden.
Multiple myeloma (MM) is an as-yet incurable B-cell malignancy. Increased survival in vitro is a hallmark of MM cells, implying that a therapeutic potential may lie in circumventing antiapoptotic signals. We have previously reported that interferons (IFNs) sensitize MM cells to Fas/CD95-mediated apoptosis. In the present study, we explore the mechanism underlying this effect. In a wide screening of apoptosis-related genes, Apo2L/TRAIL (tumor necrosis factor [TNF]-related apoptosis inducing ligand) and Fas were identified as IFN targets. Sensitization to Fas-mediated apoptosis by IFNs was not affected by blocking Apo2L/TRAIL, suggesting that Apo2L/TRAIL is not a key mediator in this process. In contrast, we found that an elevated Fas expression was functionally linked to increased susceptibility to Fas-mediated apoptosis. This was further supported by the finding that IFN treatment enhanced Fas-mediated caspase-8 activation, one of the earliest signaling events downstream receptor activation. In addition, IFN treatment attenuated the interleukin 6 (IL-6)-dependent activation of signal transducer and activator of transcription 3 (Stat3), interfering with a known survival pathway in MM that has previously been linked with resistance to Fas-mediated apoptosis. Taken together, our results show that IFN-induced up-regulation of Fas sensitizes MM cells to Fas-mediated apoptosis and suggest that attenuation of Stat3 activation may be a potentially important event in this process. (Blood. 2005;106:1346-1354)
Multiple myeloma (MM) is a B-cell malignancy characterized by the accumulation of malignant plasmablasts/plasma cells in the bone marrow. Although recent therapeutic advancements have resulted in improved clinical outcomes and prolonged survival of patients with MM,1 complete remission is almost never achieved, and the disease is still considered to be incurable. New therapeutic strategies, as well as new insights regarding existing treatments, are therefore imperative.
Because MM can be characterized as a tumor composed of long-surviving rather than fast-growing malignant cells, the therapy efficacy is highly dependent on the possibility of circumventing antiapoptosis signals. It is therefore important to delineate the pathways involved in the control of MM survival and death to identify possible molecular targets of intervention. We have previously reported that MM cells are highly resistant to Fas-mediated apoptosis, but that they may be resensitized to such induction by pretreatment with interferon- Apoptosis may be triggered by 2 converging pathways (for a review, see Hengartner7). Binding of death receptors of the tumor necrosis factor receptor family, including Fas, by the corresponding ligand induces trimerization and receptor activation. This activation enables recruitment of caspase-8 to Fas-associating proteins with death domain (FADD), which induces cleavage and activation of caspase-8, ultimately leading to activation of caspase-3. A parallel pathway, the mitochondrial pathway, involves the activation and deactivation of proapoptotic and antiapoptotic B-cell lymphoma (Bcl-2) family members and converges with the death receptor pathway at the level of caspase activation. Potentially, IFN treatment may target the function or expression of components of these apoptotic pathways. Both IFNs and interleukin 6 (IL-6), an important survival factor in MM, activate signal transducer and activator of transcription (Stat) proteins, a family of transcription factors that have been associated with regulation of growth and survival of hematopoietic cells.8 On ligand binding, Stat proteins are tyrosine phosphorylated by Janus-activated kinases associated with the receptor, heterodimerize or homodimerize, translocate to the nucleus, and activate transcription of specific genes.9 Additional transcriptional control is mediated by phosphorylation of a conserved serine residue present in Stat1, Stat3, Stat4, Stat5a, and Stat5b.10 Stat3 is constitutively activated in a number of human cancers11 and has been implicated as a crucial mediator of the prosurvival function of IL-6 in MM cell lines, targeting the antiapoptotic protein Bcl-XL.12,13 In contrast, Stat1, which is activated by IFNs, has been attributed an important role in promoting apoptosis.14-17 Intriguingly, several reports suggest that Stat3 and Stat1 may counteract the effects of each other.18-20 Of particular interest for MM, Stat1 and Stat3 were shown to exert opposing effects on the transcription of Bcl-2 family members Bcl-2 and Bcl-XL.20 To determine the mechanism of IFN-induced sensitization to Fas-mediated apoptosis in MM, we investigated the effect of IFNs on the expression of candidate apoptosis-related genes. In a screening to identify IFN-regulated target genes, Apo2L/TRAIL and Fas were found to be transcriptionally regulated by IFNs. Blocking Apo2L/TRAIL had no apparent effect on IFN-induced sensitization of Fas-mediated apoptosis, suggesting that the Apo2L/TRAIL up-regulation may not be directly involved in this process. In contrast, although U-266-1970 cells already express a considerable basal level of Fas, we found that an increased level of Fas expression per se sensitizes U-266-1970 cells to Fas-mediated apoptosis. We also investigated the activity of Stat3 and found that IFNs inhibited the IL-6-induced activation of Stat3, indicating an additional level at which IFNs can affect the survival of MM cells.
Cell lines and primary cells
The IL-6-dependent MM cell lines U-266-197021,22 and U-195823 were maintained at 37°C in 5% CO2 in RPMI 1640 medium (Sigma Biosciences, St Louis, MO) supplemented with 10% heat-inactivated fetal bovine serum (Gibco, Grand Island, NY), 2 mM glutamine, and antibiotics (penicillin 100 U/mL, streptomycin 50 µg/mL; Sigma Biosciences). Cells were routinely grown on a layer of the IL-6-producing human fibroblast line AG1523 (Human Mutant Genetic Cell Repository, Camden, NJ) or in medium supplemented with 20 U/mL IL-6 (R&D Systems Europe, Abington, United Kingdom). Experiments were performed on exponentially growing cells, induced by IL-6 (R&D Systems Europe) alone or in combination with IFN- RPA
Cells were harvested and total RNA (5 µg/sample) was isolated using the RNAgents Total RNA Isolation System (Promega, Madison, WI). Ribonuclease protection assays (RPAs) were performed according to the manufacturer of RiboQuant Multi-Probe RNase Protection Assay System (PharMingen, San Diego, CA) using Quantitative real-time PCR
Primary CD138+ plasma cells (0.5-1 x 106) from patients with MM were treated as indicated for 24 hours immediately following purification. Total cellular RNA was isolated using TRIzol reagent (Life Technologies, Paisley, United Kingdom). RNA quantity and quality was analyzed using the RNA 6000 Nano Assay, (Agilent Technologies, Waldbronn, Germany). cDNA was prepared by First-Strand cDNA Synthesis using SuperScript III for reverse transcription-polymerase chain reaction (RT-PCR; Invitrogen, Carlsbad, CA). The mRNA expression levels of Fas/Apo1, TRAIL/Apo2L, and Western blotting
Cells were harvested and washed in phosphate-buffered saline (PBS); lysates were prepared and analyzed by Western blot as previously described.24 Primary antibodies used were Analysis of apoptosis and Fas protein expression by flow cytometry
Cells were incubated with 20 U/mL IL-6 alone or in combination with 1000 U/mL IFN- Caspase-8 activity assay
U-266-1970 cells were incubated with 20 U/mL IL-6 alone or in combination with 1000 U/mL IFN- Determination of Fas expression in living cells treated with agonistic anti-Fas antibody CH-11
U-266-1970 cells were incubated with IL-6 (20 U/mL) alone or in combination with IFN- Sorting of cells according to Fas expression U-266-1970 cells were preincubated with IL-6 and stained with UB-2 anti-Fas antibody and FITC-conjugated secondary antibody as described. The cells were sorted by flow cytometry according to Fas expression and divided into 3 groups designated "high Fas" (comprising the upper 25%), "low Fas" (the lower 25%), and "all Fas" (excluding only PI+ cells). After 96 hours, the cells were treated with CH-11 or IgM overnight. The proportion of apoptotic cells and the Fas expression were determined by flow cytometry as described (see "Analysis of apoptosis and Fas protein expression by flow cytometry"). Plasmids The pcDNA3.1-CD95 plasmid (designated pcDNA3-Fas) was a kind gift from Dr T. H. Landowski.29 The empty pcDNA3.1 vector was used as a negative control, and pcDNA3.1.EGFP expressing green fluorescent protein (GFP) was used as a marker for transfection. Transfections The cells were transfected using the Amaxa Nucleofector apparatus (Amaxa, Cologne, Germany). Briefly, 2 x 106 U-266-1970 cells were grown without antibiotics for 24 hours, washed once in cold PBS, and resuspended in 100 µL electroporation buffer R with 3 µg pcDNA3-Fas or empty vector, together with 1 µg pcDNA3.1.EGFP. The cell suspension was transfected using program U-05. In a separate experiment, pcDNA3-Fas was substituted for pDsRed2-C1 expressing red fluorescent protein (BD Biosciences), enabling us to determine that under these conditions, 65% of the enhanced GFP (EGFP+) cells coexpress both the transfected vectors (data not shown). At 24 hours after transfection, the cells were treated with CH-11 or control IgM for the indicated time and subjected to flow cytometry analysis of apoptosis as described (see "Analysis of apoptosis and Fas protein expression by flow cytometry"), gating for EGFP+ cells. Fas expression in EGFP+ cells was determined by flow cytometry 24 hours after transfection, using the UB2 antibody as described together with an APC-labeled goat antimouse secondary antibody (BD Biosciences). EMSA
For electrophoretic mobility shift assay (EMSA), nuclear lysates were prepared as described by Andrews and Faller30 and 5 µg/lane was incubated with 32P-labeled double stranded m67SIE probe in a DNA-binding reaction (20 mM HEPES [N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid], pH 7.9, 40 mM KCl, 1 mM MgCl2, 0.1 mM EGTA [ethylene glycol tetraacetic acid], 10% glycerol, 0.5 mM dithiothreitol, 2 µg poly(dIdC)) for 30 minutes on ice. To identify specific DNA-binding proteins, nuclear extracts were preincubated with 2 µg Statistical analysis Statistical analysis was done by analysis of variance (ANOVA) followed by multiple comparison by the Fisher method using StatView software (Cary, NC).
Bcl-2 and Bcl-XL levels are not down-regulated by IFNs in U-266-1970
Expression of antiapoptotic Bcl-2 family proteins, such as Bcl-2 and Bcl-XL, has previously been associated with apoptosis resistance in MM.12,31,32 Interestingly, IFN-induced apoptosis of MM cells has been correlated with Bcl-XL down-regulation and Bcl-2 cleavage.31 To investigate the possibility that IFN treatment sensitizes MM cells to Fas-mediated apoptosis through regulation of Bcl-2 family proteins, we performed an RPA using RNA prepared from IFN-induced U-266-1970 cells and the hAPO-2c template set (Figure 1, Figure S1A). A slight up-regulation of proapoptotic Bax and Bak and antiapoptotic Bcl-X and Mcl-1 mRNA was noted in response to IFN- Turning to other potential targets of IFN, we performed RPAs using multiprobe template sets covering a variety of apoptosis-related genes. Using the hAPO-6 template set, containing among others Harakiri, apoptosis signal-regulating kinase 1, death associated protein (DAP), and DAP kinase, quantification did not detect any substantial (> 2 times) changes in gene expression during IFN-treatment in U-266-1970 cells (Figure 1B, Figure S1B, and data not shown). A strong up-regulation of TRAIL and a modest up-regulation of Fas are detected after IFN-treatment in U-266-1970 cells and in primary MM cells
Next, we examined the transcriptional regulation of a number of genes that are more directly associated with death-receptor signaling. The template sets hAPO-3b (Figure 1C and Figure S1C) and hAPO-3c (Figure 1D) both contain caspase-8, receptor-interacting protein (RIP), Fas, and FasL. RIP is a proapoptotic protein implicated in caspase-independent pathways during Fas-mediated apoptosis.33 RIP mRNA expression was transiently increased at early times in response to IFN treatment, but the expression had returned to basal level before 96 hours after induction, when sensitization to Fas-mediated apoptosis is most pronounced (Figure 1G). A moderate up-regulation of Fas mRNA, up to 4 times, was seen in response to both IFN-
Transcription of c-FLIP, encoding a caspase-8 binding inhibitor of death receptor-induced apoptosis, was slightly up-regulated by IFN-
Interestingly, the TNF-related apoptosis-inducing ligand (Apo2L/TRAIL) was rapidly and potently up-regulated in response to both IFN-  (> 100 times) and IFN- (6 times; Figure 1D,G), while remaining at a fairly constant level in the presence of IL-6 alone (Figure 1E). IFN--induced up-regulation of Apo2L/TRAIL was also confirmed on the protein level (Figure 2A). In contrast, the regulation of Apo2L/TRAIL protein in response to IFN- was less evident (in agreement with a modest mRNA up-regulation) and could only be detected at longer exposure (data not shown). The expression of Apo2L/TRAIL receptors DR5 and DR4 remained unaffected.
To determine whether the IFN-induced regulation of gene expression in U-266-1970 is a unique property of this particular cell line, we studied the transcriptional response to IFNs in the MM cell line U-1958. These cells share several features with the U-266-1970 cell line, including IL-6 dependence and the ability to be sensitized for Fas-mediated apoptosis by pretreatment with IFNs.2 Using RPAs with the multiprobe templates hAPO-2c, hAPO-3b, and hAPO-3c, we found that U-1958 cells respond similarly to IFNs as U-266-1970 cells, exhibiting a modest up-regulation of Fas and a strong up-regulation of Apo2L/TRAIL in response to both IFN-
To study the regulation of Apo2/TRAIL and Fas mRNA expression in primary MM cells, purified CD138+ cells from 11 patients with MM were subjected to treatment with IL-6 alone or in combination with IFN-
The sensitizing effect of IFNs on Fas-mediated apoptosis cannot be blocked by inhibiting TRAIL
IFN-
Twenty-four hours of incubation with the agonistic anti-Fas antibody CH-11 resulted in 27% apoptotic cells, whereas pretreatment with IFN- IFN-induced sensitization of MM cells to Fas-mediated apoptosis is associated with an increased activation of caspase-8
Apo2L/TRAIL and Fas-mediated signaling pathways converge downstream of caspase-8 activation, eventually leading to apoptosis. However, IFN treatment sensitizes MM cells to Fas-mediated apoptosis, but not TRAIL-induced apoptosis (data not shown). Therefore, we reasoned that at least part of the sensitizing effect of IFNs must be associated with Fas-specific signaling events up-stream of caspase-8 activation. We analyzed the effect of IFNs on caspase-8 activation by Western blot by comparing the cleavage of caspase-8 in IFN-treated cells following Fas and TRAIL stimulation. Interestingly, we found that IFN treatment enhanced Fas-mediated cleavage of caspase-8, suggesting that IFN-induced sensitization of Fas-mediated apoptosis does indeed occur up-stream to caspase-8 activation (Figure 5A). To further monitor caspase-8 activity, we analyzed caspase-8-induced cleavage of Ile-Glu-Thr-Asp-p-nitroanilin (IETD-pNA) using the BD ApoAlert Caspase Colorimetric Assay Kit. In concordance with an increased cleavage of caspase-8, we found that IFN treatment augmented caspase-8 activation following Fas stimulation (Figure 5B). The IFN-induced increase in caspase-8 activation occurred only in response to Fas stimulation, and a similar increase was not evident when cells were treated with IFNs in combination with TRAIL or control IgM. Instead, IFN-
High Fas expression correlates to increased sensitivity to Fas-mediated apoptosis Given the specific increase in Fas-mediated caspase-8 activity in response to IFN treatment, we wanted to analyze if IFN-induced sensitization occurred at the level of receptor activation. Fas expression is moderately increased by IFN treatment, whereas a substantial basal expression of Fas is detected on untreated cells (Figure 6A top panel). However, after treatment with the agonistic anti-Fas antibody CH-11, the remaining IFN-treated viable cells express approximately equal levels of Fas on their surface as untreated cells (Figure 6A lower panel). This prompted us to investigate if cells expressing high levels of Fas were more prone to undergo Fas-mediated apoptosis. U-266-1970 cells with a high or low expression of Fas were separated using FACS. After sorting, the cells were allowed to recover for 4 days. The cells were then incubated with CH-11 for 24 hours and an annexin V/PI apoptosis assay was performed (Figure 6B). Interestingly, cells expressing a higher level of Fas were more sensitive to Fas-mediated apoptosis (26% apoptotic cells) than cells expressing a lower level of Fas (11% apoptotic cells).
Increased Fas-expression per se sensitizes MM cells to Fas-mediated apoptosis These results encouraged us to directly address if a moderate increase in Fas expression, comparable to what is detected after IFN treatment, would sensitize cells to Fas-mediated apoptosis. We transfected U-266-1970 cells with a Fas expression vector or empty vector, together with an EGFP expression vector as a marker for transfection, and compared the ability of transfected cells to undergo Fas-mediated apoptosis. At 24 hours after transfection, the cells were analyzed for Fas expression, left untreated, or incubated with CH-11 for 24 hours. An annexin V/PI apoptosis assay was performed on untreated or CH-11-induced cells, gating for EGFP+ cells. Interestingly, the moderate increase in Fas expression in cells cotransfected with pcDNA3-Fas (Figure 6C) was coupled to a significantly increased sensitivity to Fas-mediated apoptosis (33% apoptotic cells) as compared to cells transfected with empty vector (22% apoptotic cells; Figure 6D).
IFN-
It has previously been suggested that Stat3, induced by the MM survival factor IL-6, is a crucial mediator of MM survival, including resistance to Fas-mediated apoptosis.12 Interestingly, Stat3, in a complex with c-Jun, has been shown to negatively regulate Fas expression, whereas Stat1 activation has been associated with increased transcriptional activation of the Fas promoter.35,36 To examine the possible role of STAT regulation in IFN-induced sensitization to Fas-mediated apoptosis in MM, we determined the effect of IFN treatment on the expression and activity of Stat1 and Stat3 transcription factors. We stimulated U-266-1970 cells with IFNs for different time periods and analyzed the levels of tyrosine phosphorylated Stat1 and Stat3 proteins. Because U-266-1970 cells are IL-6 dependent, well representing the in vivo situation, we also stimulated the cells with IL-6. As expected, IFN-
IFNs have the potential to influence growth and survival in MM, on their own, or in synergy with other agents. Delineating the pathways involved in IFN simulation may lead to an increased understanding of MM tumor development and to definition of possible targets for therapeutic intervention. We have previously shown that IFNs can sensitize U-266-1970 MM cells for Fas-mediated apoptosis.2 In the current study, we explored the mechanism of this effect and the downstream effectors involved. In a wide screening for IFN-induced, apoptosis-associated genes, Apo2L/TRAIL and Fas were identified. These genes were also up-regulated in primary MM cells stimulated with IFN. We could not find any evidence supporting an involvement of Apo2L/TRAIL in the sensitization to apoptosis mediated by Fas. In contrast, an elevated level of Fas expression was associated with an increased susceptibility to Fas-mediated apoptosis. This finding was emphasized by the observation that MM cells could be sensitized to Fas-mediated apoptosis through Fas transfection alone. However, our data also suggest that IFNs may regulate additional targets regulating survival of these cells and that some of these potential targets may be activated downstream Stat1 or Stat3 signaling events.
Apo2L/TRAIL has been shown to induce apoptosis of MM cell lines and freshly isolated MM cells and has also been suggested to mediate IFN- Our results indicate that an up-regulation of a specific part of the Fas death pathway, namely, the receptor itself, is an underlying mechanism in IFN-induced sensitization to Fas-mediated apoptosis. The observed IFN-induced Fas up-regulation in U-266-1970 cells does not reflect an increased percentage of Fas-expressing cells but rather an increased overall expression.2 The relevance of an increased Fas expression in these cells is not obvious. The relatively abundant basal expression of Fas on the surface of U-266-1970 is not reflected in a high degree of sensitivity to Fas-mediated apoptosis, which would imply that the amount of Fas is unlikely to be a limiting factor. Furthermore, many studies have pointed out the lack of correlation between the Fas expression in myeloma cell lines and their respective sensitivity to Fas-mediated apoptosis.37-39 Nevertheless, our data show that an increased basal expression of Fas, either in a subpopulation of U-266-1970 cells or in Fas-transfected cells, is indeed associated with a higher sensitivity to Fas-mediated apoptosis in U-266-1970 cells. This suggests that the IFN-induced shift to a more sensitive phenotype is mechanistically linked to an up-regulation of Fas. This is in accordance with a previous study by Shain et al, showing that clonal variability in Fas expression determines sensitivity to Fas-mediated apoptosis in RPMI 8226 MM cells.40 However, the increase in Fas-mediated apoptosis observed when Fas was ectopically expressed was, although clearly significant, less dramatic than that observed after IFN treatment, implying that the sensitization by IFNs may involve additional mechanisms. It should be noted that the cotransfection efficiency obtained under these conditions is 65%. Therefore, the enhanced apoptosis sensitivity due to ectopic Fas expression is likely to be underestimated. The finding that IFN treatment, in addition to activating Stat1, attenuated Stat3 activation in MM cells is, to our knowledge, completely new. The relevance of this finding is emphasized by the newly established role of Stat3 as a crucial prosurvival mediator in many cancers.11 In MM, IL-6-induced activation of Stat3 has been associated with resistance to apoptosis, including Fas-mediated apoptosis.12 Conversely, inhibition of Stat3 by the JAK-inhibitor AG490, and, to a lesser extent, expression of dominant-negative Stat3, sensitizes U-266-1984 MM cells to Fas-mediated apoptosis.12 In contrast, the role of Stat1 in MM survival has not been elucidated. Stat1 activation has been shown to influence apoptosis in many systems by transcriptional regulation of proapoptotic genes, including several caspases.14,15,41 Importantly, Fas can be positively regulated by Stat1-dependent mechanisms in response to IFN treatment,35 whereas Stat3, in complex with c-Jun, suppresses Fas transcription.36 Interestingly, it has been suggested that the balance between Stat1 and Stat3 could influence survival by exerting opposing effects on the expression of the very same gene, including the Bcl-2 gene and the Bcl-XL gene.20 Our results imply that in MM, IFN-induced activation of Stat1 may, directly or indirectly, counteract Stat3 activation and thus overcome resistance to Fas-mediated apoptosis by shifting the balance from activation of prosurvival genes in favor of proapoptotic ones. However, aside from Fas, these target genes have yet to be elucidated. Studies investigating the precise role of STAT regulation in MM apoptosis resistance are currently underway.
We thank Pernilla Martinsson, Charlotta Sandberg, and Sevinc Koyuncu for excellent technical assistance, and Dr T. H. Landowski, Genentech, and Immunex for kindly providing DNA constructs and reagents.
Submitted April 8, 2004; accepted April 6, 2005.
Prepublished online as Blood First Edition Paper, April 28, 2005; DOI 10.1182/blood-2004-04-1322.
Supported by grants from the Swedish Cancer Society, the Multiple Myeloma Research Foundation (MMRF), von Kantzows stiftelse, Magnus Bergwalls stiftelse, and Göran Gustafssons stiftelse.
The online version of the article contains a data supplement.
The publication costs of this article were defrayed in part by page charge payment. Therefore, and solely to indicate this fact, this article is hereby marked "advertisement" in accordance with 18 U.S.C. section 1734.
Reprints: Helena Jernberg Wiklund, Department of Genetics and Pathology, Rudbeck Laboratory, S-751 85 Uppsala, Sweden; e-mail: helena.jernberg_wiklund{at}genpat.uu.se.
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Top
Abstract
Introduction
-actin were quantified using TaqMan gene expression "Assays on Demand" (ID Hs00531110 m1, Hs00234355 m1). Quantitative real-time PCR was performed using TaqMan Universal Master Mix. Thermal cycling conditions were 95°C for 10 minutes, 40 times (95°C for 15 seconds, 60°C for 60 seconds). Relative mRNA expression was calculated using the comparative cycle time method.
