A MT1-MMP/NF-κB signaling axis as a checkpoint controller of COX-2 expression in CD133(+) U87 glioblastoma cells
- Borhane Annabi†1,
- Carl Laflamme†1,
- Asmaa Sina1,
- Marie-Paule Lachambre2 and
- Richard Béliveau2Email author
© Annabi et al; licensee BioMed Central Ltd. 2009
Received: 17 February 2009
Accepted: 09 March 2009
Published: 09 March 2009
The CD133(+) stem cell population in recurrent gliomas is associated with clinical features such as therapy resistance, blood-brain barrier disruption and, hence, tumor infiltration. Screening of a large panel of glioma samples increasing histological grade demonstrated frequencies of CD133(+) cells which correlated with high expression of cyclooxygenase (COX)-2 and of membrane type-1 matrix metalloproteinase (MT1-MMP).
We used qRT-PCR and immunoblotting to examine the molecular interplay between MT1-MMP and COX-2 gene and protein expression in parental, CD133(+), and neurospheres U87 glioma cell cultures.
We found that CD133, COX-2 and MT1-MMP expression were enhanced when glioma cells were cultured in neurosphere conditions. A CD133(+)-enriched U87 glioma cell population, isolated from parental U87 cells with magnetic cell sorting technology, also grew as neurospheres and showed enhanced COX-2 expression. MT1-MMP gene silencing antagonized COX-2 expression in neurospheres, while overexpression of recombinant MT1-MMP directly triggered COX-2 expression in U87 cells independent from MT1-MMP's catalytic function. COX-2 induction by MT1-MMP was also validated in wild-type and in NF-κB p65-/- mutant mouse embryonic fibroblasts, but was abrogated in NF-κB1 (p50-/-) mutant cells.
We provide evidence for enhanced COX-2 expression in CD133(+) glioma cells, and direct cell-based evidence of NF-κB-mediated COX-2 regulation by MT1-MMP. The biological significance of such checkpoint control may account for COX-2-dependent mechanisms of inflammatory balance responsible of therapy resistance phenotype of cancer stem cells.
Despite significant improvements, current therapies have yet to cure infiltrative gliomas. Therapy resistance is possibly attributable to cancer stem cells (CSC), a small subpopulation of cells within the brain tumor mass responsible for the initiation and maintenance of the tumor . Recently, small populations of CSC in adult and pediatric brain tumors were identified and, once isolated from tumor tissues, formed neurospheres when cultured in vitro [2, 3]. Based upon their high expression of the neural precursor cell surface marker CD133 (prominin-1), these CSC have been further hypothesized to bear properties such as resistance to apoptosis and resistance to both drugs and ionizing radiation [4, 5]. While the brain tissue microenvironmental niche is a prerequisite for expression of the stem cell marker CD133 antigen in brain tumors , its expression level is also thought to predict clinical outcome in glioma patients [7, 8].
High cyclooxygenase (COX)-2 expression is another condition associated with clinically more aggressive gliomas and is, along with CD133, a strong predictor of poor survival [9, 10]. COX-2 is an inducible enzyme responsible for prostaglandin production at sites of inflammation [11, 12]. In human glioblastoma, COX-2 performs important functions in tumorigenesis  and inhibitors of eicosanoid biosynthesis have been shown to suppress cell proliferation and to promote astrocytic differentiation . Since COX-2 protein is overexpressed in the majority of gliomas, it is therefore considered to be an attractive therapeutic target [15, 16]. In fact, enhancement of glioblastoma radioresponse by the selective COX-2 inhibitor celecoxib was recently reported . Paradoxically, the effectiveness of COX-2 inhibitors on glioma cell proliferation and radioresponse enhancement was also found to be independent of COX-2 protein expression . This evidence suggests that alternate signaling molecules are associated to therapy resistance and involved in regulating COX-2 expression. These alternate molecules may possibly become attractive therapeutic targets.
Membrane-type matrix metalloproteinases (MT-MMP) constitute a growing subclass of MMP . While most of the MMP are secreted, the MT-MMP are membrane-associated and a number of these have cytoplasmic domains which are important in cellular signaling [20–22]. MT1-MMP is the best-characterized MT-MMP. In addition to activation of proMMP-2, MT1-MMP displays intrinsic proteolytic activity towards extracellular matrix (ECM) molecules. The increased expression levels of several members of the MMP family have been shown to correlate with the graded level of gliomas, including MT1-MMP. Aside from its classical roles, many new functions of MT1-MMP were recently demonstrated, including a role in PGE2-induced angiogenesis , platelet-mediated calcium mobilization , regulation of cell death/survival bioswitch [22, 25], and radioresistance in both glioma cells [26, 27] and endothelial cells . Finally, the recent demonstration that MT1-MMP also plays a role in medulloblastoma CD133(+) neurosphere-like formation and increased invasiveness  reinforces the need to design new therapeutic strategies that either directly target MT1-MMP functions or its associated signaling functions.
In the present study, we examined whether CD133(+) U87 glioma cells are characterized by increased COX-2 and MT1-MMP expression, and whether a potential MT1-MMP/COX-2 signalling axis might be important with respect to the therapy-resistant phenotype of CSC.
Sodium dodecylsulfate (SDS) and bovine serum albumin (BSA) were purchased from Sigma (Oakville, ON). Cell culture media was obtained from Invitrogen (Burlington, ON). Electrophoresis reagents were purchased from Bio-Rad (Mississauga, ON). The enhanced chemiluminescence (ECL) reagents were from Amersham Pharmacia Biotech (Baie d'Urfé, QC). Micro bicinchoninic acid protein assay reagents were from Pierce (Rockford, IL). The polyclonal antibodies against CD133 and COX-2, and the monoclonal antibody against GAPDH were purchased from Abcam (Cambridge, MA) and Advanced Immunochemical Inc. (Long Beach, CA) respectively. The polyclonal antibody against MT1-MMP (AB815) was from Chemicon (Temecula, CA). Horseradish peroxidase-conjugated donkey anti-rabbit and anti-mouse IgG secondary antibodies were from Jackson ImmunoResearch Laboratories (West Grove, PA). All other reagents were from Sigma-Aldrich Canada.
Cell culture and neurosphere-like formation
The human U87 glioblastoma cell line was purchased from American Type Culture Collection (Manassas, VA) and was maintained in Eagle's Minimum Essential Medium (EMEM) containing 10% (v/v) calf serum (CS) (HyClone Laboratories, Logan, UT), 2 mM glutamine, 100 units/ml penicillin and 100 mg/ml streptomycin. Cells were incubated at 37°C with 95% air and 5% CO2. Neurosphere-like formation was triggered in a defined serum-free neural stem cell medium  containing Ex Vivo 15 (Lonza, Walkersville, MD), 20 ng/ml basic fibroblast growth factor, 20 ng/ml of epidermal growth factor (Wisent, St-Bruno, QC), 20 ng/ml leukemia inhibitory factor (Sigma, Oakville, ON) and 1× neural survival factor-1 (Lonza, Walkersville, MD). Murine L929 (L) cells were maintained as previously described . NF-κB p50-/- and p65-/- immortalized fibroblasts were obtained from Dr David Baltimore (California Institute of Technology, Pasadena, CA, USA).
Magnetic cell sorting and flow cytometry
Confluent U87 glioma parental cells were harvested with cell dissociation buffer (Hank's based; Invitrogen), centrifuged at 800 × g for 5 min and resuspended in 1× PBS with 0.5% BSA and 2 mM EDTA. Magnetic labeling with 100 μl AC133 (CD133/1) Microbeads per 108 cells was performed for 30 minutes at 4°C using a CD133 Direct Cell Isolation kit (Miltenyi Biotec, Auburn, CA). Fifty μl of 293C3 (CD133-2)-phycoerythrin (fluorochrome-conjugated mouse monoclonal IgG2b; Miltenyi Biotec) was added for an additional 10 min at 4°C to evaluate the efficiency of magnetic separation by flow cytometry. Magnetic separation was carried out using LS columns and a MACS separator (Miltenyi Biotec) under a biological hood. CD133(+) fractions were eluted by removing the colunm from the magnetic field and using a sterile plunger. Aliquots of CD133(+)-sorted cells were evaluated for purity by flow cytometry with a FACSCalibur machine (BD Biosciences). CD133(+)-sorted cell populations were resuspended in SFM with growth hormones.
Total RNA isolation and quantitative reverse transcription-polymerase chain reaction (qRT-PCR) analysis
Total RNA was extracted from monolayers or neurosphere-like cells using TRIzol reagent (Life Technologies). For cDNA synthesis, 1 μg total RNA was reverse-transcribed into cDNA using a high capacity cDNA reverse transcription kit (Applied Biosystems, Foster City, CA). cDNA was stored at -80°C until PCR. Gene expression was quantified by real-time quantitative PCR using iQ SYBR Green Supermix (BIO-RAD, Hercules, CA). DNA amplification was carried out using an Icycler iQ5 machine (BIO-RAD, Hercules, CA) and product detection was performed by measuring the binding of the fluorescent dye SYBR Green I to double-stranded DNA. All the primer sets were provided by QIAGEN (Valencia, CA). The relative quantities of target gene mRNA against an internal control, 18S ribosomal RNA, was measured by following a ΔCT method. An amplification plot comparing fluorescence signal vs. cycle number was drawn. The difference (ΔCT) between the mean values in the triplicate samples of target gene and those of 18S ribosomal RNA were calculated by iQ5 Optical System Software version 2.0 (BIO-RAD, Hercules, CA) and the relative quantified value (RQV) was expressed as 2ΔCT.
RNA interference experiments were performed using HiPerFect (QIAGEN, Valencia, CA). A small interfering RNA (siRNA; 20 nM) against MT1-MMP (siMT1-MMP) and mismatch siRNA were synthesized by EZBiolab Inc. (Westfield, IN), and annealed to form duplexes. The sequence of the siMT1-MMP used in this study was derived from the human MT1-MMP gene (NM_004995) and is as follows: 5'-CCAGAAGCUGAAGGUAGAAdTdT-3' (sense) and 5'-UUCUACCUUCAGCUUCUGGdTdT-3' (antisense) . Evaluation of the transient knockdown duration was performed by real-time quantitative RT-PCR and the targeted gene expression was found to be routinely diminished by 65–90% 24 to 48 hrs post-transfection (not shown).
Cell transfection method
Sub-confluent U87 monolayer cells were transiently transfected with 10 μg of the cDNA encoding full length (Wt) MT1-MMP fused to GFP  using Lipofectamine 2000 (Invitrogen, Burlington, ON). Mock transfections of U87 cultures with the empty vector, pcDNA (3.1+), were used as controls. Transfected cells were left to recuperate and were used 48 hrs post-transfection. MT1-MMP specific gene expression and function was evaluated by semi-quantitative RT-PCR and immunoblotting procedures, and was validated by assessing MT1-MMP-mediated proMMP-2 activation by gelatin zymography.
Gelatin zymography was used to assess the extracellular levels of proMMP-2 and MMP-2 activities. Briefly, an aliquot (20 μl) of the culture medium was subjected to SDS-PAGE in a gel containing 0.1 mg/ml gelatin. The gels were then incubated in 2.5% Triton X-100 and rinsed in nanopure distilled H2O. Gels were further incubated at 37°C for 20 hrs in 20 mM NaCl, 5 mM CaCl2, 0.02% Brij-35, 50 mM Tris-HCl buffer, pH 7.6 and then stained with 0.1% Coomassie Brilliant blue R-250 and destained in 10% acetic acid, 30% methanol in H2O. Gelatinolytic activity was detected as unstained bands on a blue background.
Proteins from control and treated cells were separated by SDS-polyacrylamide gel electrophoresis (PAGE). After electrophoresis, proteins were electrotransferred to polyvinylidene difluoride membranes which were then blocked for 1 hr at room temperature with 5% non-fat dry milk in Tris-buffered saline (150 mM NaCl, 20 mM Tris-HCl, pH 7.5) containing 0.3% Tween-20 (TBST). Membranes were further washed in TBST and incubated with the primary antibodies (1/1,000 dilution) in TBST containing 3% bovine serum albumin, followed by a 1 hr incubation with horseradish peroxidase-conjugated anti-rabbit or anti-mouse IgG (1/2,500 dilution) in TBST containing 5% non-fat dry milk. Immunoreactive material was visualized by enhanced chemiluminescence (Amersham Biosciences, Baie d'Urfée, QC).
CD133, COX-2 and MT1-MMP expression is increased in neurosphere-like U87 glioma cultures
Cell-based evidence that MT1-MMP directly regulates COX-2 expression in U87 glioma cell lines
CD133-sorted U87 glioma cells grow as neurospheres and express high levels of COX-2
MT1-MMP-mediated regulation of COX-2 expression is independent of MT1-MMP's catalytic functions
COX-2 induction by MT1-MMP occurs through NF-κB-mediated mechanisms
Overexpression of COX-2, the enzyme responsible for the synthesis of prostaglandin subtype PGE2, has been found to be important in the development of several human tumor types such as colon, gastric, pancreatic, and brain tumors [9, 37], and has also been associated with high tumor aggressiveness and poor patient prognosis [15, 38]. In cell studies, the growth rate of glioblastoma multiforme (GBM) cells correlated with the level of COX-2 enzyme expression, and PGE2 is thought to inhibit these cells' apoptosis  and to act as a radioprotector [40, 41]. As GBM is a high-grade primary brain tumor that is refractory to current forms of treatment possibly due to the presence of tumor-derived CSC, such molecular and cellular attributes may therefore reflect the CSC therapy resistance phenotype. In light of our results showing increased expression of COX-2 in CD133(+) U87-derived glioma cells as well as in CD133-enriched U87 neurospheres, it could be hypothesized that this molecular signature may, in part, be responsible for the therapy resistance phenotype attributable to CSC.
Membrane-type matrix metalloproteinases (MT-MMP) constitute a growing subclass of MMP, with MT1-MMP being the best-characterized MT-MMP whose expression correlates with high-grade gliomas . Aside from its well-established roles in the activation of proMMP-2 and its intrinsic proteolytic activity towards ECM molecules, many new functions of MT1-MMP have recently been demonstrated which include a role in PGE2-induced angiogenesis  as well as radioresistance in glioma cells [26, 27]. The recent demonstration that MT1-MMP also plays a role in medulloblastoma CD133(+) neurosphere-like formation and increased invasiveness  further supports the concept of a molecular interplay between MT1-MMP and COX-2. Besides glioblastoma cells, such a link has also been observed in cells derived from malignant fibrous histiocytoma, one of the highest-grade sarcomas arising in bone and soft tissue, where concomitant increased levels of expression of COX-2 and of MT1-MMP were described . Overexpression of COX-2 was also found to elevate tumorigenicity, tumor growth and invasion of human KB carcinoma cells via up-regulated MT1-MMP activity . Finally, co-distribution of MT1-MMP, MMP-2 and COX-2 was demonstrated in grade IV atheroma, again indicating a possible link between these enzymes in the destabilization of atherosclerotic plaques . Altogether, these published data suggest a molecular signaling convergence linking COX-2 to MT1-MMP expression.
By virtue of its ability to regulate the expression of genes involved in cell apoptosis, differentiation, adhesion, and survival, NF-κB constitutes the point of convergence of many oncogenic pathways . Aside from its critical role in the development of human cancer, NF-κB has also been implicated at the molecular level in the promotion of angiogenesis, which is of particular interest since malignant astrocytomas are highly vascular tumors . NF-κB is also a transcriptional regulator of inducible expression of genes including COX-2 . Interestingly, a consensus binding site for NF-κB p65 (TGGAGCTTCC) was found in the 5'-flanking region of the human MT1-MMP gene  and NF-κB-mediated induction of MT1-MMP was confirmed in murine melanoma cells  and in human fibrosarcoma cells . Further studies also implicated NF-κB as a potentially critical factor in astrocytic tumorigenesis and astrocytoma progression through analysis of cell lines and preclinical models [51–53]. NF-κB functions as a hetero- or homo-dimer which can be formed from five NF-κB subunits, NF-κB1 (p50 and its precursor p105), NF-κB2 (p52 and its precursor p100), RelA (p65), RelB and c-Rel. The most studied dimer, p50:p65, is activated by the classical pathway and usually promotes gene expression. In the current study, we provide evidence for a MT1-MMP-mediated signaling cascade that leads to activation of COX-2 expression that is independent of MT1-MMP's catalytic function (Figure 4). We also demonstrate that this new MT1-MMP/COX-2 signaling axis, in fact, absolutely requires NF-κB p50 while knockdown of NF-κB p65 still enabled MT1-MMP to trigger COX-2 expression. In support to our results, an increase in NF-κB p50 was recently found to rapidly induce MT1-MMP expression in trabecular meshwork cells . Given MT1-MMP's well documented roles in actin/tubulin cytoskeleton perturbation associated to cell migration or tubulogenesis processes, very exciting and recent studies documented a new and underestimated role for dynein/dynactin complex in the nuclear translocation of NF-κB . Whether such microtubule involvement is affected by MT1-MMP and that would mediate specific p50 nuclear translocation certainly deserves further experimentation.
Among the therapeutic molecules that could be envisioned to target COX-2 functions in CSC, the radiosensitizing actions of meloxicam and celecoxib may be considered in light of their inhibition of PGE2 production [18, 56]. Future experimental studies on the growth inhibitory and radiosensitizing effects of these two molecules should focus on PGE2synthesis and on apoptosis induction in CSC. In fact, our present findings that COX-2 induction correlates with CD133 expression in human glioma cell lines demonstrates that selective COX-2 inhibitors may thus yield a promising perspective to further improve the therapy of glioma patients. Therefore, the development of pharmaceutical approaches that alter expression of MT1-MMP or the MT1-MMP/COX-2 signaling axis in neuroinflammation provides new biological significance that prompts in targeting invading glioma cells.
cancer stem cells
mouse embryonic fibroblasts
membrane type-1 matrix metalloproteinase
nuclear factor kappaB.
BA holds a Canada Research Chair in Molecular Oncology from the Canadian Institutes of Health Research (CIHR). AS is a Fonds de la Recherche en Santé du Québec (FRSQ) awardee. This study was funded by grants from the Natural Sciences and Engineering Research Council of Canada (NSERC) to BA, and by the CIHR and the Claude Bertrand Chair in Neurosurgery to RB.
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