Interferon-γ-induced upregulation of immunoproteasome subunit assembly overcomes bortezomib resistance in human hematological cell lines
- Denise Niewerth1,
- Gertjan JL Kaspers1,
- Yehuda G Assaraf2,
- Johan van Meerloo1, 5,
- Christopher J Kirk3,
- Janet Anderl3,
- Jonathan L Blank4,
- Peter M van de Ven6,
- Sonja Zweegman5,
- Gerrit Jansen†7 and
- Jacqueline Cloos†1, 5Email author
© Niewerth et al.; licensee BioMed Central Ltd. 2014
Received: 16 October 2013
Accepted: 6 January 2014
Published: 13 January 2014
Despite encouraging results with the proteasome inhibitor bortezomib in the treatment of hematologic malignancies, emergence of resistance can limit its efficacy, hence calling for novel strategies to overcome bortezomib-resistance. We previously showed that bortezomib-resistant human leukemia cell lines expressed significantly lower levels of immunoproteasome at the expense of constitutive proteasomes, which harbored point mutations in exon 2 of the PSMB5 gene encoding the β5 subunit. Here we investigated whether up-regulation of immunoproteasomes by exposure to interferon-γ restores sensitivity to bortezomib in myeloma and leukemia cell lines with acquired resistance to bortezomib.
RPMI-8226 myeloma, THP1 monocytic/macrophage and CCRF-CEM (T) parental cells and sub lines with acquired resistance to bortezomib were exposed to Interferon-γ for 24-48 h where after the effects on proteasome subunit expression and activity were measured, next to sensitivity measurements to proteasome inhibitors bortezomib, carfilzomib, and the immunoproteasome selective inhibitor ONX 0914. At last, siRNA knockdown experiments of β5i and β1i were performed to identify the contribution of these subunits to sensitivity to proteasome inhibition. Statistical significance of the differences were determined using the Mann-Whitney U test.
Interferon-γ exposure markedly increased immunoproteasome subunit mRNA to a significantly higher level in bortezomib-resistant cells (up to 30-fold, 10-fold, and 6-fold, in β1i, β5i, and β2i, respectively) than in parental cells. These increases were paralleled by elevated immunoproteasome protein levels and catalytic activity, as well as HLA class-I. Moreover, interferon-γ exposure reinforced sensitization of bortezomib-resistant tumor cells to bortezomib and carfilzomib, but most prominently to ONX 0914, as confirmed by cell growth inhibition studies, proteasome inhibitor-induced apoptosis, activation of PARP cleavage and accumulation of polyubiquitinated proteins. This sensitization was abrogated by siRNA silencing of β5i but not by β1i silencing, prior to pulse exposure to interferon-γ.
Downregulation of β5i subunit expression is a major determinant in acquisition of bortezomib-resistance and enhancement of its proteasomal assembly after induction by interferon-γ facilitates restoration of sensitivity in bortezomib-resistant leukemia cells towards bortezomib and next generation (immuno) proteasome inhibitors.
Bortezomib is a tight binding yet reversible proteasome inhibitor that is indicated for treatment of newly diagnosed and relapsed multiple myeloma (MM) , and is currently being tested in clinical trials for childhood leukemia . In July 2012, the epoxyketone-based proteasome inhibitor carfilzomib  was approved in the US for patients with relapsed and refractory MM who received at least two prior therapies (including bortezomib and an immunomodulatory agent) and progressed on or within 60 days of completion of the last therapy [4, 5]. Notwithstanding promising initial results, acquired resistance to bortezomib is an emerging factor, which may limit its efficacy in the treatment of hematologic malignancies. The clinical impact of acquired resistance has been demonstrated in poor responses of MM patients who were re-treated with bortezomib . Although bortezomib-retreatment was effective, the response rates as well as the duration of response were decreased as compared to initial therapy, which may point to the development of bortezomib-resistance in (a subgroup of) patients . To investigate possible mechanisms of bortezomib resistance, we previously developed in vitro cell line models of hematologic malignancies in which acquired resistance to bortezomib was provoked by chronic exposure to gradually increasing bortezomib concentrations [8, 9]. These bortezomib-resistant cell lines were characterized by an increased expression of the constitutive proteasome subunit β5 harboring mutations in the bortezomib-binding pocket, along with a decreased expression of non-mutated immunoproteasome subunits. Furthermore, these bortezomib-resistant cells displayed cross-resistance to other proteasome inhibitors that target β-subunits of the proteasome . The constitutive proteasome has three proteolytically active subunits; β5 (PSMB5), β1 (PSMB6), and β2 (PSMB7) which harbor the chymotrypsin-like, caspase-like, and trypsin-like catalytic activities, respectively. Upon exposure to inflammatory cytokines, including interferon-γ (IFN-γ) or tumor necrosis factor α (TNF-α), the constitutive subunits are exchanged for immunoproteasome subunits β5i (LMP7) β1i (LMP2), and β2i (MECL-1) . While β5i harbors chymotrypsin-like activity as in β5, whereas β2i and β2 contain trypsin-like activity, β1i displays chymotrypsin-like activity rather than β1-associated caspase-like activity [11, 12]. The immunoproteasome is dominantly expressed in cells of hematologic origin and its primary function was originally attributed to improve MHC Class I antigen presentation. To this end, the immunoproteasome can produce a distinct set of peptides from the constitutive proteasome because the immunoproteasome cleaves preferably after hydrophobic and basic amino acids (cleaved by chymotrypsin-like and trypsin-like activities, respectively) that can better fit MHC Class I molecules . Therefore, peptides generated by the immunoproteasome may be more efficient in T-cell activation than peptides from the constitutive proteasome. In addition, Seifert and colleagues  provided evidence to implicate the immunoproteasome in protein degradation after immune response-induces stress, and that the immunoproteasome is more efficient than the constitutive proteasome in controlling the protein degradation process. However, this property of immunoproteasomes was recently challenged and warrants further investigations [15, 16]. Several studies [17–19] have reported higher immunoproteasome expression compared to constitutive subunits in B-cell malignancies, underscoring the potential importance of the immunoproteasome in the homeostasis of hematologic diseases . However, although there is evidence for pre-clinical activity of the β5i-specific proteasome inhibitor ONX 0914  in experimental autoimmune disease models, data justifying its use for the treatment of hematologic malignancies is limited .
Tumor cells have the capacity to modulate immunoproteasome function to escape immune surveillance . This condition may also arise in hematologic tumor cells with acquired resistance to bortezomib due to the acquisition of mutations in the PSMB5 gene encoding the constitutive β5 subunit. Since its immunoproteasome β5i counterpart does not harbor mutations, downregulation of immunoproteasome in bortezomib-resistant hematologic tumor cell lines may provide a mechanism to escape targeting by bortezomib. From a therapeutic perspective, this would imply that tipping the balance towards upregulation of immunoproteasome expression could re-confer sensitivity to bortezomib or next generation proteasome inhibitors designed to target immunoproteasomes [20, 23].
Original studies by Altun et al  showed that inflammatory cytokines such as IFN-γ and TNFα were efficient inducers of immunoproteasomes in MM cell lines, including 8226 cells. Functional studies by Busse et al  showed that exposure to IFN-γ enhanced bortezomib-sensitivity in B-cell lines by 50%, for which the underlying mechanism was unexplored. Furthermore, the β5i immunoproteasome subunit played a critical role in IFN-γ-induced apoptosis by degradation of Mcl-1 in atherosclerotic lesion-derived cells .
In this study, we explored whether IFN-γ-induced upregulation of immunoproteasome expression in bortezomib-resistant leukemia cell lines in which both immunoproteasome expression is suppressed and mutated β5 subunits are overexpressed can serve as a therapeutic strategy to restore sensitivity towards bortezomib, carfilzomib and ONX 0914.
Human T-cell ALL CCRF-CEM cells, human myeloid leukemia THP1 cells, and human multiple myeloma RPMI-8226 cells (ATCC, Manassas, VA, USA) were cultured in RPMI-1640 medium containing 2 mM glutamine (Invitrogen/Gibco, Carlsbad, CA, USA) supplemented with 10% fetal calf serum (Greiner Bio-One, Alphen a/d Rijn, The Netherlands) and 100 μg/ml penicillin/streptomycin (Invitrogen) at 5% CO2 and 37°C. Cell cultures were seeded at a density of 3×105 cells/ml and refreshed twice weekly. Bortezomib-resistant sublines of these cell lines were established previously [8, 9]. Authenticity of bortezomib-resistant and parental cell lines was verified by STR marker analysis for D12S1045, D8S1132, D19S253, and D17S1293.
Antibodies, drugs and reagents
Antibodies to proteasome subunits β1, β2, β5, β1i, and β5i were purchased from Enzo Life Sciences (Farmingdale, NY, USA). In addition, anti-actin (clone C4) was purchased from Millipore (Temecula, CA, USA), anti-NOXA antibody from Abcam (Cambridge, UK), anti-ubiquitin (P4D1) from Santa Cruz Biotechnology (Santa Cruz, CA, USA) and the IRDye infrared secondary labeled antibodies was from LI-COR Biosciences (Lincoln, NE, USA). Bortezomib was provided by Millennium Pharmaceuticals (Cambridge, MA, USA). The epoxyketone-based proteasome inhibitors carfilzomib and ONX 0914 were provided by Onyx Pharmaceuticals, Inc. (South San Francisco, CA, USA). IFN-γ was purchased from Sanquin (Amsterdam, the Netherlands).
Proteasome active site ELISA
An ELISA-based assay (Pro-CISE) for quantitative assessment of active constitutive and immunoproteasome subunits was performed as previously described . Briefly, cell lysate was incubated with a biotinylated proteasome active-site binding probe. Lysate was then denatured, and subunits bound to probe were isolated with streptavidin-conjugated sepharose beads. Individual subunits were probed with subunit-specific primary antibodies, followed by HRP-conjugated secondary antibodies. A chemiluminescent substrate was used to generate signal associated with HRP binding, which was read on a luminometer. Absolute values of nanograms of subunit per microgram of total protein were based on a purified proteasome standard curve. Protein quantification was performed utilizing the Pierce BCA Protein Assay (Thermo Scientific, Rockford, IL, USA).
Lightcycler quantitative PCR
Lightcycler® 480 SYBR Green I Master was used to quantify expression levels of mutated and unmutated allele in the bortezomib-resistant cell lines. Primers specific for the Ala49Thr mutation, primers specific for the unmutated allele, and primers for total PSMB5 were developed (Tib-molbiol, Germany) (Additional file 1). GUS was used as housekeeping gene. All primers were used at 0.5 μM each. 5 μl of cDNA template was added to the PCR mix. Results were analysed by advanced relative quantification using the comparative cycle time (Ct) method by Lightcycler 480 Instrument Software version 1.5 (Roche Diagnostics, Switzerland).
Cell growth inhibition assay
In vitro drug sensitivity was determined using the 4-day MTT cytotoxicity assay . Prior to these experiments, bortezomib-resistant cells were cultured in bortezomib-free medium for at least 4 days. Cells were then pre-exposed for 48 h to 100 U/ml IFN-γ and then subjected to various concentrations of bortezomib (range: 0.001 μM – 2 μM), CFZ (0.008 nM - 15.6 nM for the parental cell lines; 0.0005 μM - 1 μM for bortezomib-resistant lines), or ONX 0914 (0.008 μM – 16 μM) for 4 days. For siRNA experiments, cells were incubated with 100 nM siRNA for 24 h before adding 100 U/ml IFN-γ for 48 hours, followed by the same concentration ranges of the drugs as specified above. The IC50 value was defined as the drug concentration necessary to inhibit 50% of the cell growth compared to growth of the untreated control cells.
Intact-cell based caspase-like, trypsin-like, and chymotrypsin-like proteasome activities
An intact cell-based assay to measure basal and IFN-γ-induced upregulation of caspase-like, trypsin-like, and chymotrypsin-like proteasome activities was conducted by using a Proteasome-Glo assay kit according to the manufacturer’s instructions (Promega, Madison, WI). Before determination of proteasome activity, cells were exposed to 100 U/ml IFN-γ for 24 h, 48 h, 72 h, and 96 h at 37°C in a white flat-bottomed 96-well plate (Greiner Bio-one, The Netherlands) at a density of 10 000 cells per well in a total volume of 50 μl. After 15-min incubation period with luminogenic substrates, luminescence was determined with an Infinite 200 Pro microplate reader (Tecan, Giessen, The Netherlands). Background measurements of cell-free medium plus substrate were subtracted from cell measurements.
HLA Class I expression
HLA Class I expression was determined using HLA-ABC FITC antibody (5 μg/ml) (eBioscience, San Diego, CA, USA) and mouse IgG2a antibody (5 μg/ml) as isotype control. Cells were measured on the FACSDiva, and analyzed using CELLQUEST software.
Specific β5, β5i, and β1i subunit activities in cell extracts
For measurement of specific β5, β5i, and β1i activities, the Ac-WLA-AMC, Ac-ANW-AMC, and Ac-PAL-AMC fluorogenic substrates were used, respectively . Cells were washed in ice-cold phosphate-buffered saline and 5 mM ethylenediaminetetraacetic acid (EDTA) was added at pH 8.0 and samples were frozen at -80°C until analysis. Samples were thawed and centrifuged at 10,000 g for 10 minutes at 4°C. The supernatant was removed and assayed for protein content using the BioRad Protein Assay following the manufacturer's protocol (BioRad, Hercules, CA, USA).
Assays were performed at 37°C in a final volume of 200 μL using 96-well black opaque plates (Greiner bio-one, Germany). Protein extracts were diluted to 200 μg/mL in 5 mM EDTA at pH 8.0. Diluted protein extract aliquots (50 μL) were dispensed per well, giving 10 μg of protein extract per reaction. Reactions were initiated by addition of 150 μL of 133 μM peptide-AMC substrate in 20 mM N-[2-Hydroxyethyl]piperazine-N-[2-ethanesulfonic acid] (HEPES), pH 7.4, containing 0.5 mM EDTA. Peptidase activity was measured by kinetic monitoring of 7-amino-4-methylcoumarin (AMC) production over two hours with a Biotek plate reader (Winooski, VT, USA) and analyzed by GraphPad Prism software (La Jolla, CA, USA) with linear regression analysis.
For RNA interference experiments all targeted and non-targeted siRNA constructs were obtained from Dharmacon (Lafayette, USA) and all experiments were performed in 6well plates. THP1/BTZ200 cells were cultured following the DharmaFECT general transfection protocol conditions for THP1 cells. Briefly, prior to transfection, cells were cultured overnight at a density of 3 × 105 cells/ml in RPMI-1640 medium supplemented with 10% FCS. Cells were transfected using Dharmafect 2 and 100 nM of PSMB8 or PSMB9 ON-TARGETplus SmartPool siRNA. As negative control 100 nM ON-TARGETplus siControl non-targeting siRNA was used and the GAPDH siRNA pool was included as a positive control. The transfection methods had no effect on cell growth. At several time points, transfection-efficiency was determined by mRNA expression analysis. 24 h after siRNA transfection when >80% knockdown was established, IFN-γ (100 U/ml) was added for 24 h (or 48 h when indicated), followed by bortezomib administration.
Protein expression/Western blotting
Protein expression of proteasome subunits was determined by Western blotting, as previously described . Protein bands were quantified by Odyssey software, corrected for background, and normalized by β-actin to correct for loading differences within blots.
cDNA synthesis of proteasome subunits and quantitative RT-PCR
After RNA isolation by utilizing the RNAeasy Mini kit (Qiagen, Valencia, CA, USA), cDNA was synthesized using RT buffer (Invitrogen), containing 5 mM DTT (Invitrogen), 2 mM dNTP (Roche), 96 μg/ml pdN6 (Roche), 0.75 U/μl M-MLV (Invitrogen) and 2 U/μl RNAsin (HT Biotechnology Ltd., Cambridge, UK). mRNA expression levels of proteasome subunits PSMB 5, PSMB6, PSMB7, PSMB8, PSMB9, PSMB10, and β-glucuronidase as a reference were quantified using real-time PCR analysis (Taqman) on an ABI Prism 7700 sequence detection system (PE Applied Biosystems, Nieuwerkerk a/d IJssel, The Netherlands). For PSMB5, a Taqman gene expression assay was used according to the manufacturers’ instructions (Hs00605652_m1, Applied Biosystems). All other primers and probes were designed using Primer Express software (Applied Biosystems) and are indicated in Additional file 1. Probes were labeled with 5’-FAM and 3’-BHQ1 as a reporter. Real-time PCR was performed in a total reaction volume of 25 μl containing TaqMan buffer A (Applied Biosystems), 4 mM MgCl2, 0.25 mM of each dNTP (Amersham Pharmacia Biotech) and 1.25 U AmpliTaq Gold DNA polymerase (Applied Biosystems). Samples were heated for 10 min at 95°C to activate the AmpliTaq Gold DNA polymerase and amplified during 40 cycles of 15 s at 95°C and 60 s at 60°C. Relative mRNA expression levels of the target genes in each sample were calculated using the comparative cycle time (Ct) method. The Ct of the target gene was normalized to the GUS Ct value by subtracting the GUS Ct value from the target Ct value. The mRNA expression level for each target PCR relative to GUS was calculated using the following equation: mRNA expression = 2(Ct target-Ct GUS) × 100%.
where 1 INF = 0 and 1 for experiments without and with IFN-γ, respectively. The parameters Max, IC 50 , and Hill model the maximum of the percentage growth, the concentration at which the percentage growth is 50% of the maximum and the slope of the curve for the experiments without IFN-γ. Parameters ΔMax, ΔIC 50 , and ΔHill model the change in these parameters as a result of adding IFN-γ. Our models included additive random effects for replicate and a residual error which were assumed to be normally distributed and independent. Nonlinear mixed models were fitted in SAS version 9.2 separately for each drug and cell line combination.
Statistical significance of the differences in subunit expression and proteasome activity were determined using the Mann-Whitney U test. Statistical significance was achieved when P < 0.05. Statistical analyses were performed using SPSS (version 20.0).
Characterization of bortezomib-sensitive and bortezomib-resistant hematologic tumor cell lines
IFN-y exposure tips balances from constitutive proteasomes to immunoproteasomes
Collectively, bortezomib-resistant hematologic tumor cells possess the capacity to markedly induce immunoproteasome levels upon IFN-γ stimulation, thereby outweighing mutated and unmutated constitutive proteasome levels.
IFN-γ stimulation confers increased proteasome catalytic activity and HLA Class-I molecule expression
IFN-γ promotes sensitization of bortezomib-resistant cell lines to cell death by proteasome inhibitors
Immunoproteasome subunit β5i is responsible for the sensitization of bortezomib-resistant cell lines
The present study is the first to document the impact of IFN-γ on constitutive- and immunoproteasome homeostasis in three bortezomib-resistant tumor cell lines of different hematologic origin and to assess the implications for anti-proliferative activity of proteasome inhibitors. Characteristically, the bortezomib-resistant cell lines largely expressed the mutated form of PSMB5, and clearly, IFN-γ increased the expression of catalytically active immunoproteasome levels in bortezomib-resistant cells with concurrent downregulation of both mutated and unmutated alleles of constitutive β5. This property facilitated sensitization to bortezomib, and an even more pronounced sensitization to the immunoproteasome inhibitor ONX 0914. Sensitization effects were most prominent in 8226/BTZ cells and lowest in CEM/BTZ cells, which may be related to the fact that CCRF-CEM leukemia cells have low levels of IFN-γ receptors . At equal doses of IFN-γ, induction of immunoproteasome β5i and β1i subunit mRNA and protein expression was significantly higher (up to 4-fold) in bortezomib-resistant tumor cells compared to parental cells. Concomitantly, constitutive proteasome subunits were clearly downregulated at a protein level, but not as much on mRNA levels. This phenomenon was also reported by others (reviewed by Ebstein et al ), indicating that downregulation of constitutive subunits involves a post-transcriptional mechanism. Nonetheless, by employing a very sensitive lightcycler RT-PCR technique, a moderate downregulation on mRNA level was detectable. Additionally, in PBMCs from healthy individuals, the same results were noticed as in the parental cell lines when exposed to IFN-γ, and call for further analyses in bortezomib-resistant patient specimen. It is not clear whether the upregulation of immunoproteasome levels reflects a compensatory and homeostatic effect after initial downregulation during bortezomib resistance development. Importantly, increased β5i expression can drive incorporation of immunoproteasome subunits into prototypic immunoproteasomes  or facilitate assembly in hybrid types of proteasomes (β1 + β2 + β5i and β1i + β2 + β5i) . Conceivably, these hybrid forms could compensate for impaired catalytic activity of constitutive proteasomes assembled with a mutated β5-subunit. Following use of β5-selective substrates, chymotrypsin-like catalytic activity in cell extracts of bortezomib-resistant cells increased 2-4 fold over those of parental cells (Figure 3B). These observations are consistent with our previous report in which we observed, using native gel electrophoresis, proficient catalytic capacity of mutated β5 subunit-harboring proteasomes in CEM/BTZ cells for chymotrypsin-like probes, but a diminished inhibitory capacity by bortezomib . Likewise, Kale et al  showed that strains of the marine actinobacterium Salinispora tropica could maintain self-resistance to the proteasome inhibitor salinosporamide A by expressing a proteasome variant harboring β5 subunit mutations similar to those detected in human THP1/BTZ cells [8, 9]. This mutated β5 subunit had retained its capacity to hydrolyze β5-specific substrates, but displayed a diminished sensitivity to inhibition by salinosporamide A.
The expanding knowledge of factors determining bortezomib sensitivity or resistance that emerged from cell line studies (reviewed in ref ), still awaits translation and implementation in a clinical setting. With respect to the role of immunoproteasomes, a recent report from our laboratory showed that higher ratios of immunoproteasome over constitutive proteasome in acute leukemia patient samples served as an important parameter for their ex vivo sensitivity to bortezomib and ONX 0914 . In addition, Shuqing et al  showed an increase in constitutive PSMB5 mRNA expression in a myeloma patient after bortezomib treatment compared to the pre-treatment sample. Also recently, Leung-Hagensteijn et al  showed that immunoproteasome subunit expression was decreased in patients with myeloma tumors resistant to bortezomib, compared to bortezomib-sensitive patients. This study also revealed that the loss of Xbp1 signaling (which is required for plasma cell differentiation and regulation of unfolded protein response) induced bortezomib-resistance in MM cell lines and patient cells. Based on these considerations, strategies that may increase immunoproteasome levels may merit further exploration for therapeutic intervention.
Despite the fact that IFN-γ-induced upregulation of immunoproteasomes facilitates sensitization of bortezomib-resistant cells to bortezomib and ONX 0914, IFN-γ exposure does not establish full restoration of parental sensitivity to bortezomib. This may be due to two reasons; first, inhibition of the catalytic activity of the immunoproteasome alone appears insufficient to exert a cell growth inhibitory effect. Rather, this requires inhibition of chymotrypsin-like activity and co-inhibition of caspase-like or trypsin-like activities [38, 39]. Second, the constitutive β5 subunit is structurally altered in all 3 bortezomib-resistant tumor cell lines due to mutations in the PSMB5 gene introducing single amino acid substitutions (e.g. Ala49Thr) in the bortezomib-binding pocket leading to diminished bortezomib binding efficiency [8, 9]. This structural alteration precludes optimal inhibition of the β5 subunit by bortezomib as present in parental cells, thus retaining a significant degree of bortezomib resistance. These considerations specifically apply for cells with a high level (> 100-fold) of bortezomib resistance. In cells (e.g. 8226/BTZ7 cells) with a more clinically relevant low level (~ 5-fold) resistance to bortezomib, IFN-γ exposure reversed 50% of bortezomib resistance and achieved parental sensitivity to ONX 0914 (Figure 4D, Additional file 7). The latter observation is consistent with data from Huber et al  who showed that incorporation of immunoproteasome subunits confers structural alterations in the 20S proteasome complex, resulting in improved accessibility of ONX 0914 to the active sites, which would underlie a mechanism for the largest differential sensitizing effect observed with ONX 0914 as compared to bortezomib and carfilzomib.
Knockdown experiments revealed that β5i expression is critically involved in mediating the proteasome inhibitor-sensitizing effects in bortezomib-resistant tumor cells. The role of β5i may first be related to proteasome assembly, in which β5i is required for processing the β1i and β2i subunits . Consistently, β5i deficiency delays immunoproteasome assembly . Beyond increased immunoproteasome subunit expression after IFN-γ exposure, chymotrypsin-like and trypsin-like proteasome catalytic activities were increased, whereas caspase-like activity was decreased. Employing subunit activity-specific probes indicated that the increase in chymotrypsin-like activity was solely accountable for by the increase in β5i but not β5 catalytic activity. At the same time, the decrease in caspase-like activity was solely due to reduced β1 activity since β1i activity actually increased upon stimulation with IFN-γ. Thus, our findings in bortezomib-resistant cells underscore studies showing that replacement of β1 with β1i decreased caspase-like activity and enhanced β5i-associated chymotrypsin-like activity [11, 12, 42]. Immunologically, a rise in chymotrypsin-like activity would result in the generation of more peptides with hydrophobic C-terminal residues for presentation on MHC class-I molecules . As such, a prominent IFN-γ-induced switch from constitutive to immunoproteasomes in bortezomib-resistant cells could lead to gain of efficiency in antigen presentation by increased peptide loading after immunoproteasome peptide processing. In our study, PSMB8/ β5i-downregulation resulted in a 50% decrease of chymotrypsin-like activity, whereas β1i downregulation had no effect on any of the three catalytic activities (data not shown). This phenotype seems fully compatible with that of β5i-deficient mice displaying a 50% decrease in the expression of MHC class-I molecules; these alterations were not observed in β1i- or β2i-deficient mice [13, 43, 44].
Krüger and Kloetzel  suggested that IFN-γ induction combines enhanced translational activity with a rapid increase in the pool of polyubiquitinated proteins that require processing by the proteasome. In this context, the IFN-γ-induced synthesis of immunoproteasomes may represent a physiological adaptation to this cytokine-induced oxidative stress. If cells under these conditions were to be exposed to proteasome inhibitors, blocking of functional activity of newly formed immunoproteasomes would result in additional accumulation of polyubiquitinated proteins, causing cell stress and induction of apoptotic cell death. The bortezomib-resistant cell lines did reveal accumulation of polyubiquitinated proteins as in bortezomib-sensitive parental cells but at higher bortezomib concentrations to which they are adjusted [8, 9]. This is likely due to an adaptive mechanism in bortezomib-resistant cells to enhance the β5-associated catalytic capacity to process physiological substrates (Figure 3B). Interference with this process by IFN-γ induced upregulation of immunoproteasomes and blocking their function with specific inhibitors could then trigger accumulation of polyubiquitinated proteins and apoptotic cell death, hence being in line with the mechanism proposed by Kruger and Kloetzel .
Downregulation of β5i subunit expression was identified as being an important determinant of acquisition of bortezomib resistance in cell lines of hematologic malignancies. The pharmacological implication of this novel finding is exemplified by the fact that induction of β5i proteasomal assembly after IFN-γ exposure facilitated restoration of sensitivity of bortezomib-resistant cells towards bortezomib and in particular to immunoproteasome inhibitors.
This study was supported by research funding from the Netherlands Organization for Scientific Research, and KiKa (Children Cancer-free) grant number 51 (G.J.L.K).
- Laubach JP, Schlossman RL, Mitsiades CS, Anderson KC, Richardson PG: Thalidomide, lenalidomide and bortezomib in the management of newly diagnosed multiple myeloma. Expert Rev Hematol. 2011, 4: 51-60. 10.1586/ehm.10.83.View ArticlePubMedGoogle Scholar
- Niewerth D, Dingjan I, Cloos J, Jansen G, Kaspers GJL: Proteasome inhibitors in acute leukemia. Expert Rev Anticancer Ther. 2013, 13: 327-337. 10.1586/era.13.4.View ArticlePubMedGoogle Scholar
- Demo SD, Kirk CJ, Aujay MA, Buchholz TJ, Dajee M, Ho MN, Jiang J, Laidig GJ, Lewis ER, Parlati F, Shenk KD, Smyth MS, Sun CM, Vallone MK, Woo TM, Molineaux CJ, Bennett MK: Antitumor activity of PR-171, a novel irreversible inhibitor of the proteasome. Cancer Res. 2007, 67: 6383-6391. 10.1158/0008-5472.CAN-06-4086.View ArticlePubMedGoogle Scholar
- Siegel DS, Martin T, Wang M, Vij R, Jakubowiak AJ, Lonial S, Trudel S, Kukreti V, Bahlis N, Alsina M, Chanan-Khan A, Buadi F, Reu FJ, Somlo G, Zonder J, Song K, Stewart AK, Stadtmauer E, Kunkel L, Wear S, Wong AF, Orlowski RZ, Jagannath S: A phase 2 study of single-agent carfilzomib (PX-171-003-A1) in patients with relapsed and refractory multiple myeloma. Blood. 2012, 120: 2817-2825. 10.1182/blood-2012-05-425934.PubMed CentralView ArticlePubMedGoogle Scholar
- Kortuem KM, Stewart AK: Carfilzomib. Blood. 2013, 121: 893-897. 10.1182/blood-2012-10-459883.View ArticlePubMedGoogle Scholar
- Kumar SK, Lee JH, Lahuerta JJ, Morgan G, Richardson PG, Crowley J, Haessler J, Feather J, Hoering A, Moreau P, Leleu X, Hulin C, Klein SK, Sonneveld P, Siegel D, Blade J, Goldschmidt H, Jagannath S, Miguel JS, Orlowski R, Palumbo A, Sezer O, Rajkumar SV, Durie BG: Risk of progression and survival in multiple myeloma relapsing after therapy with IMiDs and bortezomib: a multicenter international myeloma working group study. Leukemia. 2012, 26: 149-157. 10.1038/leu.2011.196.PubMed CentralView ArticlePubMedGoogle Scholar
- Hrusovsky I, Emmerich B, von Rohr A, Voegeli J, Taverna C, Olie RA, Pliskat H, Frohn C, Hess G: Bortezomib retreatment in relapsed multiple myeloma - results from a retrospective multicentre survey in Germany and Switzerland. Oncology. 2010, 79: 247-254. 10.1159/000322866.View ArticlePubMedGoogle Scholar
- Oerlemans R, Franke NE, Assaraf YG, Cloos J, van Zantwijk I, Berkers CR, Scheffer GL, Debipersad K, Vojtekova K, Lemos C, van der Heijden JW, Ylstra B, Peters GJ, Kaspers GJL, Dijkmans BA, Scheper RJ, Jansen G: Molecular basis of bortezomib resistance: proteasome subunit beta5 (PSMB5) gene mutation and overexpression of PSMB5 protein. Blood. 2008, 112: 2489-2499. 10.1182/blood-2007-08-104950.View ArticlePubMedGoogle Scholar
- Franke NE, Niewerth D, Assaraf YG, Van Meerloo J, Vojtekova K, van Zantwijk CH, Zweegman S, Chan ET, Kirk CJ, Geerke DP, Schimmer AD, Kaspers GJL, Jansen G, Cloos J: Impaired bortezomib binding to mutant beta5 subunit of the proteasome is the underlying basis for bortezomib resistance in leukemia cells. Leukemia. 2012, 26: 757-768. 10.1038/leu.2011.256.View ArticlePubMedGoogle Scholar
- Aki M, Shimbara N, Takashina M, Akiyama K, Kagawa S, Tamura T, Tanahashi N, Yoshimura T, Tanaka K, Ichihara A: Interferon-gamma induces different subunit organizations and functional diversity of proteasomes. J Biochem. 1994, 115: 257-269.PubMedGoogle Scholar
- Groettrup M, Ruppert T, Kuehn L, Seeger M, Standera S, Koszinowski U, Kloetzel PM: The interferon-gamma-inducible 11 S regulator (PA28) and the LMP2/LMP7 subunits govern the peptide production by the 20S proteasome in vitro. J Biol Chem. 1995, 270: 23808-23815. 10.1074/jbc.270.40.23808.View ArticlePubMedGoogle Scholar
- Schmidtke G, Eggers M, Ruppert T, Groettrup M, Koszinowski UH, Kloetzel PM: Inactivation of a defined active site in the mouse 20S proteasome complex enhances major histocompatibility complex class I antigen presentation of a murine cytomegalovirus protein. J Exp Med. 1998, 187: 1641-1646. 10.1084/jem.187.10.1641.PubMed CentralView ArticlePubMedGoogle Scholar
- Groettrup M, Kirk CJ, Basler M: Proteasomes in immune cells: more than peptide producers?. Nat Rev Immunol. 2010, 10: 73-78. 10.1038/nri2687.View ArticlePubMedGoogle Scholar
- Seifert U, Bialy LP, Ebstein F, Bech-Otschir D, Voigt A, Schroter F, Prozorovski T, Lange N, Steffen J, Rieger M, Kuckelkorn U, Aktas O, Kloetzel PM, Kruger E: Immunoproteasomes preserve protein homeostasis upon interferon-induced oxidative stress. Cell. 2010, 142: 613-624. 10.1016/j.cell.2010.07.036.View ArticlePubMedGoogle Scholar
- Nathan JA, Spinnenhirn V, Schmidtke G, Basler M, Groettrup M, Goldberg AL: Immuno- and constitutive proteasomes do not differ in their abilities to degrade ubiquitinated proteins. Cell. 2013, 152: 1184-1194. 10.1016/j.cell.2013.01.037.PubMed CentralView ArticlePubMedGoogle Scholar
- Ebstein F, Voigt A, Lange N, Warnatsch A, Schröter F, Prozorovski T, Kuckelkorn U, Aktas O, Seifert U, Kloetzel P-M, Krüger E: Immunoproteasomes are important for proteostasis in immune responses. Cell. 2013, 152: 935-937. 10.1016/j.cell.2013.02.018.View ArticlePubMedGoogle Scholar
- Parlati F, Lee SJ, Aujay M, Suzuki E, Levitsky K, Lorens JB, Micklem DR, Ruurs P, Sylvain C, Lu Y, Shenk KD, Bennett MK: Carfilzomib can induce tumor cell death through selective inhibition of the chymotrypsin-like activity of the proteasome. Blood. 2009, 114: 3439-3447. 10.1182/blood-2009-05-223677.View ArticlePubMedGoogle Scholar
- Roccaro AM, Sacco A, Aujay M, Ngo HT, Azab AK, Azab F, Quang P, Maiso P, Runnels J, Anderson KC, Demo S, Ghobrial IM: Selective inhibition of chymotrypsin-like activity of the immunoproteasome and constitutive proteasome in Waldenstrom macroglobulinemia. Blood. 2010, 115: 4051-4060. 10.1182/blood-2009-09-243402.PubMed CentralView ArticlePubMedGoogle Scholar
- Niewerth D, Franke NE, Jansen G, Assaraf YG, van Meerloo J, Kirk CJ, Degenhardt J, Anderl JL, Schimmer AD, de Haas V, Horton TM, Zweegman S, Kaspers GJL, Cloos J: Higher ratio immune vs. constitutive proteasome level as novel indicator of sensitivity of pediatric acute leukemia cells to proteasome inhibitors. Haematologica. 2013, 98: 1896-1904. 10.3324/haematol.2013.092411. doi:1896PubMed CentralView ArticlePubMedGoogle Scholar
- Kuhn DJ, Orlowski RZ: The immunoproteasome as a target in hematologic malignancies. Semin Hematol. 2012, 49: 258-262. 10.1053/j.seminhematol.2012.04.003.View ArticlePubMedGoogle Scholar
- Muchamuel T, Basler M, Aujay MA, Suzuki E, Kalim KW, Lauer C, Sylvain C, Ring ER, Shields J, Jiang J, Shwonek P, Parlati F, Demo SD, Bennett MK, Kirk CJ, Groettrup M: A selective inhibitor of the immunoproteasome subunit LMP7 blocks cytokine production and attenuates progression of experimental arthritis. Nat Med. 2009, 15: 781-787. 10.1038/nm.1978.View ArticlePubMedGoogle Scholar
- Johnsen A, France J, Sy M, Histocompatibility CIM, Lines C, Harding CV: Down-regulation of the transporter for antigen presentation, proteasome subunits, and class I major histocompatibility complex in tumor cell lines. Cancer Res. 1998, 58: 3660-3667.PubMedGoogle Scholar
- Kirk CJ: Discovery and development of second-generation proteasome inhibitors. Semin Hematol. 2012, 49: 207-214. 10.1053/j.seminhematol.2012.04.007.View ArticlePubMedGoogle Scholar
- Altun M, Galardy PJ, Shringarpure R, Hideshima T, LeBlanc R, Anderson KC, Ploegh HL, Kessler BM: Effects of PS-341 on the activity and composition of proteasomes in multiple myeloma cells. Cancer Res. 2005, 65: 7896-7901.PubMedGoogle Scholar
- Busse A, Kraus M, Na IK, Rietz A, Scheibenbogen C, Driessen C, Blau IW, Thiel E, Keilholz U: Sensitivity of tumor cells to proteasome inhibitors is associated with expression levels and composition of proteasome subunits. Cancer. 2008, 112: 659-670. 10.1002/cncr.23224.View ArticlePubMedGoogle Scholar
- Yang Z, Gagarin D, St Laurent G, Hammell N, Toma I, Hu C-A, Iwasa A, McCaffrey TA: Cardiovascular inflammation and lesion cell apoptosis: a novel connection via the interferon-inducible immunoproteasome. Arter Throm Vas. 2009, 29: 1213-1219. 10.1161/ATVBAHA.109.189407.View ArticleGoogle Scholar
- Suzuki E, Demo S, Deu E, Keats J, Rastu-Kapur S, Bergsagel PL, Bennett MK, Kirk CJ: Molecular mechanisms of bortezomib resistant adenocarcinoma cells. PLoS One. 2011, 6: e27996-10.1371/journal.pone.0027996.PubMed CentralView ArticlePubMedGoogle Scholar
- Van Meerloo J, Kaspers GJ, Cloos J: Cell sensitivity assays: the MTT assay. Methods Mol Biol. 2011, 731: 237-245. 10.1007/978-1-61779-080-5_20.View ArticlePubMedGoogle Scholar
- Blackburn C, Gigstad KM, Hales P, Garcia K, Jones M, Bruzzese FJ, Barrett C, Liu JX, Soucy TA, Sappal DS, Bump N, Olhava EJ, Fleming P, Dick LR, Tsu C, Sintchak MD, Blank JL: Characterization of a new series of non-covalent proteasome inhibitors with exquisite potency and selectivity for the 20S beta5-subunit. Biochem J. 2010, 430: 461-476. 10.1042/BJ20100383.PubMed CentralView ArticlePubMedGoogle Scholar
- Ücer U, Bartsch H, Scheurich P, Ãœcer U, Berkovic D, Ertel C, Pfizenmaier K: Quantitation and characterization of γ-interferon receptors on human tumor cells. Cancer Res. 1986, 46: 5339-5343.PubMedGoogle Scholar
- Ebstein F, Kloetzel P-M, Krüger E, Seifert U: Emerging roles of immunoproteasomes beyond MHC class I antigen processing. Cell Mol Life Sci. 2012, 69: 2543-2458. 10.1007/s00018-012-0938-0.View ArticlePubMedGoogle Scholar
- Heink S, Ludwig D, Kloetzel PM, Kruger E: IFN-gamma-induced immune adaptation of the proteasome system is an accelerated and transient response. Proc Natl Acad Sci U S A. 2005, 102: 9241-9246. 10.1073/pnas.0501711102.PubMed CentralView ArticlePubMedGoogle Scholar
- Vigneron N, Van den Eynde BJ: Proteasome subtypes and the processing of tumor antigens: increasing antigenic diversity. Curr Opin Hematol. 2012, 24: 84-91.Google Scholar
- Kale AJ, McGlinchey RP, Lechner A, Moore BS: Bacterial self-resistance to the natural proteasome inhibitor salinosporamide A. ACS Chem Biol. 2011, 6: 1257-1264. 10.1021/cb2002544.PubMed CentralView ArticlePubMedGoogle Scholar
- Kale AJ, Moore BS: Molecular mechanisms of acquired proteasome inhibitor resistance. J Med Chem. 2012, 55: 10317-10327. 10.1021/jm300434z.PubMed CentralView ArticlePubMedGoogle Scholar
- Shuqing L, Jianmin Y, Chongmei H, Hui C, Wang J: Upregulated expression of the PSMB5 gene may contribute to drug resistance in patient with multiple myeloma when treated with bortezomib-based regimen. ExpHematol. 2011, 39: 1117-1118.Google Scholar
- Leung-Hagesteijn C, Erdmann N, Cheung G, Keats JJ, Stewart AK, Reece DE, Chung KC, Tiedemann RE: Xbp1s-negative tumor B cells and pre-plasmablasts mediate therapeutic proteasome inhibitor resistance in multiple myeloma. Cancer Cell. 2013, 24: 289-304. 10.1016/j.ccr.2013.08.009.PubMed CentralView ArticlePubMedGoogle Scholar
- Singh AV, Bandi M, Aujay MA, Kirk CJ, Hark DE, Raje N, Chauhan D, Anderson KC: PR-924, a selective inhibitor of the immunoproteasome subunit LMP-7, blocks multiple myeloma cell growth both in vitro and in vivo. Br J Haematol. 2011, 152: 155-163. 10.1111/j.1365-2141.2010.08491.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Britton M, Lucas MM, Downey SL, Pletnev AA, Verdoes M, Tokhunts RA, Goddard AL, Pelphrey PM, Wright DL, Overkleeft S, Kisselev AF: Selective inhibitor of proteasome’s caspase-like sites sensitizes cells to specific inhibition of chymotrypsin-like sites. Journ Chem Biol. 2009, 16: 1278-1289.View ArticleGoogle Scholar
- Huber EM, Basler M, Schwab R, Heinemeyer W, Kirk CJ, Groettrup M, Groll M: Immuno- and constitutive proteasome crystal structures reveal differences in substrate and inhibitor specificity. Cell. 2012, 148: 727-738. 10.1016/j.cell.2011.12.030.View ArticlePubMedGoogle Scholar
- Murata S, Yashiroda H, Tanaka K: Molecular mechanisms of proteasome assembly. Nat Rev Mol Cell Biol. 2009, 10: 104-115. 10.1038/nrm2630.View ArticlePubMedGoogle Scholar
- Gaczynska M, Rock KL, Spies T, Goldberg AL: Peptidase activities of proteasomes are differentially regulated by the major histocompatibility complex-encoded genes for LMP2 and LMP7. Proc Natl Acad Sci USA. 1994, 91: 9213-9217. 10.1073/pnas.91.20.9213.PubMed CentralView ArticlePubMedGoogle Scholar
- Fehling HJ, Swat W, Laplace C, Kühn R, Rajewsky K, Müller U, von Boehmer H: MHC class I expression in mice lacking the proteasome subunit LMP-7. Science. 1994, 265 (80): 1234-1237.View ArticlePubMedGoogle Scholar
- Kincaid EZ, Che JW, York I, Escobar H, Reyes-Vargas E, Delgado JC, Welsh RM, Karow ML, Murphy AJ, Valenzuela DM, Yancopoulos GD, Rock KL: Mice completely lacking immunoproteasomes show major changes in antigen presentation. Nat Immunol. 2012, 13: 129-135.View ArticleGoogle Scholar
- Krüger E, Kloetzel P-M: Immunoproteasomes at the interface of innate and adaptive immune responses: two faces of one enzyme. Curr Opin immunol. 2012, 24: 77-83. 10.1016/j.coi.2012.01.005.View ArticlePubMedGoogle Scholar
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