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Osteopontin (SPP1, a secreted phosphoprotein 1) is primarily involved in immune responses, tissue remodelling and biomineralization. However, it is also overexpressed in many cancers and regulates tumour progression by increasing migration, invasion and cancer stem cell self-renewal. Mechanisms of SPP1 overexpression in gliomas are poorly understood. We demonstrate overexpression of two out of five SPP1 isoforms in glioblastoma (GBM) and differential isoform expression in glioma cell lines. Up-regulated SPP1 expression is associated with binding of the GLI1 transcription factor to the promoter and OCT4 (octamer-binding transcription factor 4) to the first SPP1 intron of the SPP1 gene in human glioma cells but not in non-transformed astrocytes. GLI1 knockdown reduced SPP1 mRNA and protein levels in glioma cells. GLI1 and OCT4 are known regulators of stem cell pluripotency. GBMs contain rare cells that express stem cell markers and display ability to self-renew. We reveal that SPP1 is overexpressed in glioma initiating cells defined by high rhodamine 123 efflux, sphere forming capacity and stemness marker expression. Forced differentiation of human glioma spheres reduced SPP1 expression. Knockdown of SPP1, GLI1 or CD44 with siRNAs diminished sphere formation. C6 glioma cells stably depleted of Spp1 displayed reduced sphere forming capacity and downregulated stemness marker expression. Overexpression of the wild type Spp1, but not Spp1 lacking a Cd44 binding domain, rescued cell ability to form spheres. Our findings show re-activation of the embryonic-type transcriptional regulation of SPP1 in malignant gliomas and point to the importance of SPP1-CD44 interactions in self-renewal and pluripotency glioma initiating cells.
Osteopontin/SPP1, a secreted phosphoprotein 1, acts via integrin receptors and the glycoprotein CD44, and regulates adhesion, migration, invasion, chemotaxis and cell survival . Multi-functionality of osteopontin is due to the presence of different isoforms, generated by an alternative splicing, and various post-translational modifications such as phosphorylation, sulfation, glycosylation and protelytic cleavage. The levels of SPP1 mRNA are up-regulated in many malignant cancer tissues, and elevated levels of SPP1 in patients’ tumour tissue and blood are associated with poor prognosis [2, 3]. SPP1 modulates many functions of cancer cells: it stimulates cancer cell proliferation and invasion, and supports tumour angiogenesis [4, 5] and distant tumour outgrowth by instigating dormant tumours . On the other hand, SPP1 expression is increased under acute and chronic inflammatory conditions, wound repair and fibrosis. SPP1 is implicated in chemotaxis and recruitment of immune cells to inflamed sites, and production of inflammation mediators by immune cells [7, 8]. These various and to some extent opposing functions of SPP1 are attributed to its differential posttranscriptional processing in normal and transformed cells [9–11].
Glioblastoma (GBM) is the most common primary brain tumour in adults and its treatment remains a major challenge for clinicians because these aggressive and invasive tumours are highly resistant to radio- and chemotherapy . Previous studies reported the elevated expression of three SPP1 isoforms in tumour tissues and sera from GBM patients, and found an inverse correlation of its expression with patient survival [13–16]. Isoforms of SPP1 displayed different effectiveness in stimulation of glioma invasion and cell survival . GBM contains a subpopulation of glioma initiating cells (GIC) with stem cell features and an ability to self-renew. These cells are believed to contribute to therapy resistance and tumour recurrence [18, 19]. A couple of recent studies demonstrated the important role of autocrine and paracrine SPP1-CD44 signalling in maintenance of glioma initiating cells [20, 21].
Despite numerous reports regarding SPP1 up-regulation in many cancers, there is a scarce information regarding the transcriptional regulation of SPP1, in particular in cancer stem cells. The SPP1 expression is regulated mainly at the level of transcription . Deletion analyses of the SPP1 gene promoter and gel shift studies demonstrated c-Myc and OCT-1 binding to the proximal promoter of SPP1 gene in U251MG and U87MG human glioma cells . Transcription factors ETS-1 and RUNX2 regulated SPP1 expression in colorectal cancer cells . In melanoma cells transcription factors c-Myb , AML-1a and C/EBPα bind to the SPP1 gene promoter  and the transcription factor GLI1, a mediator of Hedgehog (HH) signalling have been shown to regulate SPP1 expression . Transcriptional regulation of SPP1 in GBM cells and its role in GIC compartment needs further clarification.
In this study we present the expression pattern of five SPP1 isoforms in low and high grade gliomas, five glioma cell lines and non-transformed astrocytes, and transcriptional regulation of SPP1 by stemness transcription factors GLI1 and OCT4, expressed in glioblastoma cells, but not in normal astrocytes. Moreover, we report up-regulation of the SPP1 expression in glioma initiating cells, defined by high efflux capacities, sphere forming abilities and the upregulated expression of stemness markers. In glioma sphere cultures undergoing forced differentiation the expression of SPP1 was reduced. Using siRNA and shRNA-mediated gene interference we demonstrated the involvement of SPP1/osteopontin in glioma sphere formation and the importance of SPP1-CD44 interactions.
Previous studies have determined the expression of SPP1-a,-b,-c isoforms in tumour tissues [2, 3]. Examination of SPP1 records in the NCBI database (http://www.ncbi.nlm.nih.gov/gene/6696) shows the presence of five isoforms of this gene. We determined their expression in normal brains (n = 5, one being a mixture of 24 RNA samples), benign juvenile pilocytic astrocytomas (PA, WHO grade I, n = 20) and highly malignant glioblastomas (GBM, WHO grade IV, n = 57). SPP1-e (former SPP1-a) and SPP1-d isoforms were significantly overexpressed in GBMs (Figure (Figure1A).1A). The analysis of TCGA (The Cancer Genome Atlas) data set confirmed these results. Kaplan-Meyer survival plot derived from TCGA data illustrates negative correlation between high SPP1 expression and survival time (Figure (Figure1B).1B). The expression of SPP1 did not differ significantly between four GBM subtypes (Supplementary Figure S1). A distinctive expression pattern of SPP1 isoforms was detected in a panel of human glioma cells when compared to normal astrocytes (NHA). The expression of all SPP1 isoforms was increased in U87MG glioma cells, SPP1-c, -d, -e mRNA levels were upregulated in LN229 glioma cells; GBM patient-derived WG4 cells had the higher SPP1-c level in comparison to non-transformed human astrocytes. T98G and LN18 glioblastoma cells had lower levels of SPP1 mRNAs than astrocytes (Figure (Figure1C).1C). A scheme in the Figure Figure1D1D depicts exons and corresponding protein domains present in various SPP1 isoforms as well as sites of potential interactions with other proteins. The SPP1-e mRNA encodes a full length protein, while SPP1-d mRNA encodes the SPP1 isoform lacking 4, 5 and 6 exons.
We performed a computational analysis of the human SPP1 promoter region using the Nencki Genomics Database  which integrates information about sequence motifs and epigenetic modifications in the non-coding regions, conserved between human, rat and mouse. Two putative GLI1 binding sites were identified in the human SPP1 gene promoter (Figure (Figure2A).2A). GLI1 (Glioma-Associated Oncogene Homolog 1) is a transcription factor activated downstream Hedgehog signalling pathway. We demonstrated binding of GLI1 to the proximal promoter of SPP1 gene by chromatin immunoprecipitation (ChIP) assay in three human glioma cell lines, including primary human WG4 glioma cultures, but not in NHA (Figure (Figure2B).2B). Knockdown of GLI1 expression in glioma cells (Figure (Figure2C)2C) significantly reduced the levels of SPP1 mRNA and protein production (Figure 2D–2E).
A stemness factor Oct4 was shown to bind within the first intron of the murine Spp1 gene  and regulate its expression in murine embryonic cells. Using chromatin immunoprecipitation we found binding of the OCT4 protein to the first intron of the SPP1 gene in human glioma cells, but not in NHA (Figure (Figure2F).2F). Effective binding of RNA Polymerase II to the constitutive promoter was assessed as a positive control to ensure a good quality of the immunoprecipitated DNA from NHA (Figure (Figure2F).2F). We have attempted silencing of the OCT4 expression with the specific siRNA, however, due to barely detectable OCT4 levels in glioma cells, we could not verify its knockdown by Western blotting.
The levels of GLI1 and OCT4 mRNAs were determined in the same samples of normal brain, pilocytic astrocytomas and glioblastomas analyzed for SPP1 expression. The GLI1 mRNA level was significantly up-regulated in GBMs in comparison to low grade tumors and normal brains. The OCT4 expression was detectable in all tested tumors and was not significantly different in GBMs versus PAs (Figure (Figure2G).2G). The presented results show co-expression and binding of GLI1 and OCT4 transcription factors to the SPP1 gene. The transcriptional regulation of the SPP1 expression by GLI1 (and likely OCT4) in glioma cells resembles the stem cell-type regulation.
Transcription factors GLI1 and OCT4 are involved in a control of self-renewal of both somatic stem cells and cancer stem cells . The observed regulation of SPP1 expression by stemness transcription factors led us to quantify the SPP1 mRNA levels (specifically SPP1-e, a full form of SPP1) in a subpopulation enriched in glioma initiating cells (GIC). These cells are implicated in tumour formation and recurrence [30, 31]. To obtain a subpopulation enriched in GIC, we isolated a side population (SP) using a Rhodamine123 (Rhod123) exclusion assay and flow cytometry. Stem-like cells exclude dyes more efficiently due to up-regulated expression/activity of ABC transporters . Gating strategy of the Rhod123(–) subpopulation is presented in the Supplementary Figure S2. The lower panel shows gating of the Rhod123(–) subpopulation stained with propidium iodide to control for cell viability and demonstrates a clear separation of those cells from Rhod123(+) and dead cells. It shows that FACS sorted Rhod123(–) cells were alive and excluded a Rhodamine123 dye more efficiently. Representative dot plots and histograms of sorted cells are presented in Figure Figure3A.3A. The Rhod123(–) subpopulation was detected in all tested cell lines and constituted from 3% to 8% of the total cell population in agreement with previous reports . The percentage of Rhod123(–) cells was: 8.1 ± 7.9% in T98G cells, 4.46 ± 3.56% in LN18 cells, 6.85 ± 1.05% in U87MG cells, 4.3 ± 2.9% in U373MG cells and 18.65 ± 7.39% in C6 cells.
The expression of NANOG and OCT3/4 (coding for stemness markers) in sorted Rhod123(–) subpopulation and bulk cells was measured by a quantitative PCR and considered as an indicator of GIC enrichment . The levels of NANOG and OCT3/4 mRNA were significantly higher in sorted Rhod123(–) cells than in the bulk cells in all tested glioma cultures (Figure 3B–3C). The SPP1 expression was 1000-fold up-regulated in the Rhod123(–) LN18 cells. The relative SPP1 overexpression in the Rhod123(–) subpopulation of T98G and LN18 cells versus bulk cells was similar in magnitude to SPP1 overexpression in U87MG and U373MG cells (having the highest SPP1 expression in the total cell population) when compared to NHA. The levels of Spp1, Nanog and Oct3/4 mRNAs were augmented in the Rhod123(–) cells isolated from the rat C6 glioma cultures when compared with their expression in non-transformed astrocytes (Figure (Figure3C3C).
Cancer stem cells could be grown and maintained in suspension using the neurosphere assay. These 3-D sphere cultures formed by clonally growing, anchorage-independent cells in serum-free media supplemented with specific growth factors are employed to enrich in self-renewing, multipotent cells. The resulting spheres can be expanded or forced to differentiate into cells expressing neuronal and glial differentiated cell markers . It has been demonstrated that cells growing as glioma sphere cultures are able to form tumours closely resembling human pathology when transplanted intracerebrally to immunosuppressed mice . To determine whether SPP1 is overexpressed in GIC, we measured SPP1 mRNA levels in adherent and 3-D, sphere cultures developed from human and rat glioma cells. We found the increased expression of NANOG, OCT3/4 and SPP1 mRNAs in LN18 spheres (Figure (Figure4A)4A) and C6 spheres (not shown). Western blot analysis confirmed the higher expression of stemness markers: NANOG, OCT4A and SOX2 in LN18 spheres when compared with parental flat cultures (Figure (Figure4B).4B). The expression of those markers in Ntera2 cells (human embryonic teratoma cells expressing stemness markers at very high levels) served as a positive control (Figure (Figure4B4B).
Serum and bone morphogenetic proteins (BMP) are potent inducers of glioma differentiation in vitro and in vivo, and have been shown to reduce a number of glioma initiating cells, decrease glioma proliferation and induce astrocytic or neuronal-like differentiation, respectively . We demonstrate that LN18 spheres undergo differentiation in the presence of 2% FBS or 100 ng/ml BMP4 (Figure (Figure4C).4C). Light microscopy shows morphological alterations of LN18 spheres: 5 days after treatments the cells migrated out of spheres and became flatten and adherent, in particular in the presence of 2% FBS (Figure (Figure4C).4C). Immunoflurescence analysis of spheres exposed to BMP4 shows an increase of the TUB-βIII staining (Figure (Figure4D),4D), which is consistent with neuron-like differentiation. The expression of SPP1 was significantly reduced under differentiating conditions (p = 0.0021 for serum and p = 0.0236 for BMP4 treated cultures, n = 5 experiments). Reduction of SPP1 expression was associated with the significant downregulation of NANOG expression in spheres cultured in the presence of 2% serum and OCT3/4 in BMP4 -treated spheres (Figure (Figure4E).4E). Treatment with 2% serum or to less extend with BMP4 reduced the expression of stemness genes NANOG and OCT4 to the levels detected in adherent cells (the Supplementary Figure S3). The expression of TUB-bIII did not changed significantly at the mRNA level, but we observed the increase of TUB-bIII staining intensity in BMP4 treated cultures indicative of increased protein expression (Figure (Figure4D).4D). These data demonstrate that forced differentiation of GIC cultures is associated with the reduction in the SPP1 expression.
To determine if tumour-derived SPP1 plays a role in glioma sphere formation, we knocked down its expression with the specific siRNA in cells from dissociated spheres and analysed a number of resulting secondary spheres. We demonstrated that siRNA-mediated knockdown of SPP1 expression in human LN18 cells reduced their ability to form spheres (Figure (Figure5).5). GIC spheres were counted as spheres if they reached 100–200 μm in size; quantification was performed 7 days after transfection. SPP1 knockdown in LN18 cells was very efficient (80% reduction of the SPP1 mRNA level as determined by qPCR) (Figure (Figure5A)5A) and the number of spheres was reduced by 20% (Figure (Figure5B).5B). This moderate reduction could be due to a transitory nature of SPP1 knockdown during 7 days of sphere culturing. Previous studies suggested the important role of autocrine and paracrine SPP1-CD44 signalling in maintenance of glioma initiating cells [20, 21]. To evaluate the role of GLI1-SPP1-CD44 signalling in a control of sphere formation, we knocked down the expression of GLI1 or CD44. GLI1 knockdown was verified by qPCR and CD44 knockdown was confirmed by qPCR, Western blotting and flow cytometry (Supplementary Figure S4). The efficient reduction of GLI1 or CD44 expression reduced sphere formation by 22% and 55%, respectively (Figure 5C–5D).
To achieve long term knockdown of Spp1, we developed C6 glioma cell lines stably transduced with lentiviral vectors carrying a control shNeg or shSpp1 (corresponding to a siRNA sequence). Transduced clones were sorted by flow cytometry for GFP (encoded in a lentiviral vector) to reduce cell handling before establishment of stably clones. The control shNeg cells expressed the similar level of Spp1 mRNA and protein as parental C6 glioma cells (Figure 6A, 6B). The levels of Spp1 mRNA and protein were reduced by > 90% in shSpp1 clones (Figure 6A, 6B). Knockdown of Spp1 in glioma cells did not affect basal cell viability and proliferation determined with MTT metabolism and BrdU incorporation test (Supplementary Figure S5). However, C6 glioma cells depleted of Spp1 had reduced sphere forming capacity (> 50%) (Figure 6C, 6D) and the reduced expression of stemness factors Nanog and Oct3/4 (Figure (Figure6E6E).
A recent study in a murine model of PDGFB-driven gliomas (resembling a proneural type GBM) showed that osteopontin secreted by tumour-associated astrocytes, via CD44 signalling promotes stem cell properties and glioma resistance to radiation . We demonstrate that knockdown of CD44 in glioma cells reduced sphere formation suggesting an important role of CD44-SPP1 interactions in GIC self-renewal. A C-terminus of SPP1 carries a CD44 binding site. To elucidate if the CD44 binding domain of Spp1 is critical for glioma cell capacity to self-renew, we generated constructs carrying RNA interference resistant (R) variants of a wild type Spp1 or a C-terminal truncated Spp1. These constructs were overexpressed in Spp1-depleted glioma cells and the efficient reconstitution of the Spp1 expression was achieved in transfected cells, as determined by qPCR at 48 h after transfection (Figure (Figure7A).7A). Cell proliferation of different clones overexpressing a neutral plasmid pEGFP, WtSpp1-R or Spp1ΔC-R was similar, as determined by a BrdU incorporation assay (Figure (Figure7B).7B). However, the transfected cells differed in their ability to form spheres. GIC spheres were counted 7 days after transfection. Glioma cells depleted of the endogenous Spp1 and overexpressing a neutral plasmid pEGFP failed to form spheres. Overexpression of WtSpp1-R restored glioma cell capability to form spheres, while overexpression of Spp1ΔC-R did not restore a cell ability to form spheres (Figure 7C, 7D).
The main findings of this study are: i) SPP1 overexpression in glioma initiating cells, ii) a novel mechanism of transcriptional regulation of the SPP1 by GLI1 and OCT4, and iii) demonstration of the supportive role of tumour-derived osteopontin/SPP1 in self-renewal of glioma initiating cells. We confirmed upregulated expression of a full form of SPP1 - SPP1-e in human glioblastomas and several glioma cell lines. We demonstrated that transcription factors OCT4 and GLI1, involved in maintenance of the stemness phenotype in embryonic and cancer stem cells, bind to the SPP1 gene in glioma cells, but not in normal astrocytes. This binding was detected in human glioma cell lines and GBM patient-derived WG4 cultures. The GLI1 expression was significantly upregulated in GBMs in comparison to pilocytic astrocytomas and normal brains (Figure (Figure2G).2G). Silencing of GLI1 expression with siRNA in human glioma cells reduced the levels of SPP1 expression and protein secretion. Knockdown of GLI1 significantly reduced sphere formation (Figure 5C, 5D). Binding of GLI1 to the SPP1 gene promoter was reported in metastatic melanoma cells  indicating it could be a general feature of malignant cells. The OCT4 expression was not significantly different between PA and GBM (Figure (Figure2G).2G). Due to its very low level in glioma cells, we could not demonstrate the efficacy of OCT4 silencing (not shown) and prove its role in the transcriptional SPP1 regulation. However, we demonstrate the up-regulated OCT4 expression in GIC-enriched cells isolated in the side population and in glioma sphere formation assays. We demonstrated that OCT4 binds to the regulatory element in the first intron of SPP1 gene in a manner typical for embryonic cells. Regulation of Spp1 expression by the Oct4 transcription factor, which binds to the first intron of the murine Spp1 gene, was previously demonstrated in mouse embryonic cells at an early, pre-implantation stage of development . Altogether, our results show a novel mechanism of the transcriptional SPP1 regulation, which operates in malignant tumour cells containing a subpopulation of rare cells with stemness features.
We demonstrate that even in T98G and LN18 glioblastoma cells exhibiting low levels of SPP1 expression, the expression of SPP1 is highly up-regulated in the Rhod123(–) subpopulation and glioma spheres when compared with its levels in adherent cells. Moreover, the increased SPP1 expression is associated with up-regulated NANOG and OCT3/4 mRNA levels. The higher SPP1 expression in LN18 spheres versus adherent cells is associated with the significantly increased GLI1 expression (not shown). This is the first demonstration of concomitant up-regulation of SPP1 and stemness transcription factors in glioma initiating cells.
In the present study we show the important role of tumour-derived SPP1 in stemness maintenance. We demonstrate that RNAi against SPP1 reduced the number of spheres formed by LN18 and rat C6 glioma cells, and down-regulated OCT4 and NANOG. Rat C6 glioma cells with stable knockdown of Spp1 had reduced levels of Oct3/4 and Nanog expression in sphere cultures along with the reduced sphere numbers (Figure (Figure6).6). Our observation is consistent with recently reported data demonstrating that stably knockdown of SPP1 in U87MG and GBM4371 glioma cells reduced their sphere forming capacity. The authors showed time-dependent decrease of OCT3/4, NANOG and SOX2 expression in glioma spheres after SPP1 knockdown . In murine PDGFB-induced glioma cultures and primary human GBM cultures stroma-derived osteopontin was responsible for up-regulation of NANOG, SOX2, OCT4, and ID1 expression . The crucial role of SPP1 in maintenance of human GIC stemness is strengthen by our results demonstrating the reduced SPP1 expression in LN18 sphere cultures undergoing differentiation in the presence of BMP4 or 2% FBS (Figure (Figure4).4). This is in agreement with the observations of up-regulated expression of TUJ1 and GFAP, neural differentiation markers, in GBM4371 spheres in response to 10% FBS and withdrawal of growth factors EGF and bFGF . Altogether, these data support the crucial role of ostepontin in maintaining the stemness phenotype of glioma initiating cells across various models. Undoubtedly further research is needed to verify the existence of positive loops in which SPP1 would increase the expression of OCT4 or other stemness factors, which in turn would regulate SPP1 expression. The role of SPP1 in sphere-forming capacity of cancer stem cells is likely cell type dependent. In mammary cancer spheroids blockade of osteopontin with a specific antibody decreased cell proliferation . In the hematopoietic stem cell niche osteopontin inhibited proliferation of hematopoietic stem cells  in a manner consistent with maintaining quiescence .
Our results defined mechanisms mediating SPP1 action on glioma cells. We demonstrate the importance of SPP1-CD44 interaction in maintaining the stemness phenotype as a variant of Spp1 lacking C-terminal domain responsible for interactions with CD44 was not able to restore the impaired sphere formation (Figure (Figure7).7). Using a rescue strategy, we demonstrate that overexpression of WtSpp1-R, but not Spp1ΔC-R, restored glioma cell capability to form spheres (Figure 7C, 7D). This provides evidence that the C-terminus of SPP1 carrying the CD44 binding site is critical for stemness maintaining SPP1 activity. The variant of Spp1 lacking C-terminal domain contains an intact RGD domain responsible for integrin binding. The lack of functional rescue suggests that binding of Spp1 with integrins was not sufficient to restore sphere formation capacity. CD44, a transmembrane glycoprotein, was initially identified as a receptor for hyaluronic acid, and high CD44 expression was associated with cancer stem cells and epithelial-mesenchymal transition. Previous studies have shown that CD44 expression is upregulated in GIC and the CD44high cells have higher self-renewal capacity and generate more spheres than CD44low population . We detected similar levels of CD44 mRNA and protein in adherent and spheres cultures of LN18 cells. Forced differentiation did not change CD44 expression levels (Supplementary Figure 4A). In murine model of PDGF-induced glioma osteopontin secreted by glioma-associated astrocytes enhanced the cancer stem cell phenotype through interactions with CD44 . Transcriptomic data showed that Spp1 was up-regulated specifically in glioma-associated astrocytes compared to normal astrocytes in murine PDGFB-driven gliomas and proneural human GBMs . Our data show an alternative mechanism of an autocrine action of glioma-derived SPP1/osteopontin. Despite different cell sources of SPP1/osteopontin (whether SPP1 is produced by tumour or stromal cells) all presented data confirmed the important role of osteopontin-CD44 interactions in maintaining the glioma stem cell phenotype. Our data show a novel transcriptional mechanism driving SPP1 expression in glioma cells that is not in operation in non-transformed astrocytes.
Frozen glioma biopsies were obtained from the Brain Tumour Tissue Bank (London Health Sciences Centre, CA) and Institute of Psychiatry and Neurology (IPIN) in Warsaw. Additional pilocytic astrocytoma (PA) samples and 5 normal brain tissues were obtained the Children's Memorial Health Institute, Warsaw. The study was conducted under protocol #14/KBE/2012, approved by the Research Ethics Board at IPIN.
Rat C6 and human T98G, LN18, LN229, U87 MG, U373 glioma cells, human teratocarcinoma Ntera and HeLa cells were from ATCC. Cells were passaged twice a week up to a passage 20 and were maintained for no longer than 15 weeks. Human cells were grown in DMEM with 10% foetal bovine serum (FBS) and antibiotics (50 U/ml penicillin, 50 μg/ml streptomycin); C6 cells were grown in DMEM with 10% newborn calf serum (NCS) and antibiotics as described . Normal human astrocytes were from Lonza and were cultured in the supplier-recommended medium (Lonza, CC-3186) for 2–3 weeks before experiments. Astrocyte cultures were > 98% GFAP-positive and were cultivated in DMEM with 10% FBS, passaged every week. WG4 primary glioma cultures originated from a GBM patient surgical sample. Freshly resected tumour tissue was washed in Hank's balanced sodium solution (HBSS) and subjected to mechanical and enzymatic dissociation using Neural Tissue Dissociation Kit (MiltenyiBiotec) according to the manufacturer's instructions. Tumour cells were re-suspended in DMEM F-12 supplemented with 10% FBS (Gibco) and plated at a density of 1–2 × 106 cells/60 mm plate. The fresh medium was replaced every 4 days.
ChIP assays were performed on human glioma cells and non-transformed astrocytes as previously described [42, 43]. ChIP was performed with Chip-IT Express Active Motif kit according to manufacturers’ protocol. Cells were fixed with 2% formaldehyde, sonicated with Bioruptor Plus (Diagenode) with 9 cycles 30 sec ON/OFF. Positive controls for ChIP were from Active Motif Chip-IT Control Kit Human (#53010). Antibodies for ChIP included: anti-GLI1 (Santa Cruz N-16x), anti-OCT4 (Abcam ab18976), goat IgG (Abcam ab37373), rabbit IgG (Calbiochem NI01); all antibodies were used at 3 μg per reaction. The following ChIP-PCR primers were used: for the OCT4 binding site in the first intron of SPP1 gene forward CACCTAAGTAGCACCTACTTG, reversed CCTACAAACAGATCAACAGTAAC and for the GLI1 binding site in the SPP1 gene promoter: forward CTGACAGAAAATCCTACTCAGAAAA, reversed: AAA GTAGGAAATGGATGCTGCG. Two putative GLI1 binding sites have been identified in the SPP1 promoter using MathInspector (Genomatix, Germany) and the Ensembl funcgen database as described . ChIP primers were designed for both putative sites but only the binding to the proximal GLI binding site of the SPP1 gene was confirmed. Primers for the potential OCT4 binding site in the first intron of the SPP1 gene corresponded to the Oct4 binding site in the murine Spp1 gene previously described . The PCR products were resolved in 1% agarose gel with ethidium bromide and visualized with UV light.
For side population isolation, Rhodamine 123 (Rhod123) exclusion assay was performed. Glioma cells from the earliest passages were trypsinized and 107 cells were incubated with 0.1 μg/ml Rhod123 (in DMSO, Sigma) for 20 min in 37°C. Cells were rinsed, re-suspended in 0.5 ml of medium and placed in 37°C for 90 min for Rhod123 exclusion. A portion of cells kept on ice to inhibit the exclusion of Rhod123 served as a positive control. Fractions of Rhod123(+) and (–) cells were sorted using FACS Aria (Becton Dickinson, USA) and collected in Qiagen RLT lysis buffer. We did not observe any significant increase in the number of dead cells in our preparation, cell debris were removed from quantification by appropriate gating as previously described . For the experiment presented in the Supplementary Figure S3B, prior to a flow cytometry analysis the cells were labelled with 5 μg/ml of propidium iodide to determine numbers of live/dead cells.
For sphere forming assay, cells were seeded at a low density (4000 or 8000 cells/ml of medium) onto non-adherent plates and cultured in DMEM/F-12 medium (Gibco, 31331-028), supplemented with B27 (Gibco, 0080085SA), 20 ng/ml bFGF (Miltenyi Biotec), 20 ng/ml EGF (Stemcell Technologies) and antibiotics. After 7 or 14 days resulting spheres were collected by centrifugation at 1500 rpm and lysed in Qiagen RLT lysis buffer.
For differentiation experiments, spheres were maintained for 8 days in the sphere culture medium followed by incubation for 5 days in the presence of 100 ng/ml BMP4 (Sigma-Aldrich, Germany) or 2% FBS.
Western blot analysis was performed as previously described . Primary antibodies included: anti-SOX2, anti-OCT4A (Cell Signaling Technology, Beverly MA, USA), anti-NANOG (Cell Signaling Technology, Beverly MA, USA). Immunocomplexes were visualized using ECL (Amersham, Germany). The membranes were stripped and re-probed with horseradish peroxidase-conjugated anti-β-actin antibody (1:10000, #A3854 Sigma-Aldrich, Saint Louis, MO, USA). The molecular weight of proteins was estimated with pre-stained protein markers (Sigma-Aldrich, Saint Louis, MO, USA). CD44 was detected by Western blotting with polyclonal Sheep IgG anti-human CD44 (#AF3660, R&D System, Minneapolis, MN, USA, 1:500) followed by a rabbit Anti-Sheep IgG-HRP conjugate (#AP147P, Merck Millipore KGaA, Darmstadt, Germany, 1:5000). For flow cytometry we used Alexa Fluor 700 Mouse Anti-Human CD44 Clone G44-26 RUO (#561289, BD Pharmingen); Alexa Fluor 700 Mouse IgG2b, κ Isotype Control RUO (#560543, BD Pharmingen).
For immunofluorescence analysis, cells grown on coverslips were fixed with 4% paraformaldehyde (PFA). After blocking for 1 h with 0.1% Triton X-100 containing 1% bovine serum albumin, sections were incubated with anti-β Tubulin III antibody (Millipore, Temecula, CA, USA) diluted in 1% bovine serum albumin containing 0.1% Triton X-100 at 4°C overnight. Reactions were visualized by incubating with a secondary, anti-mouse antibody conjugated to Alexa-555 (Life Technologies, Karlsruhe Germany). Cells were counterstained with 1 μg/ml DAPI and images were acquired with Olympus X70 fluorescent microscope.
Total RNA was isolated from glioma cells using Qiagen RNeasy kit, 1 μg was used as a template. Amplifications were performed in duplicates in 20 μl containing 2× SYBR PCR MasterMix (Applied Biosystems) and a set of primers (human SPP1, NANOG and POU5F1_1_SG/OCT4 primers were from QuantiTect Primer Assays: QT01008798, QT01844808 and QT00210840, respectively, Qiagen). Sequences of primers for rat Spp1 stemness and differentiation genes are in the Table Table1.1. The amount of target mRNA was normalized to the 18S rRNA amplified from the same sample. Data were analysed using the Relative Quantification (ΔΔCt) method with 7500 System SDS software (Applied Biosystems).
LN18 cultures were transfected with 25 nM SMARTpool: siGENOME SPP1 siRNA and siGENOME Non-Targeting siRNA Pool #1 (Thermo Scientific) using DharmaFECT. Transfection efficacy estimated with a rhodamine labelled control siRNA was 89%. Osteopontin levels in glioma conditioned media were determined by ELISA (#ADI-900-142, ENZO Life Sciences). Human GLI1 was knocked-down using ON-Target PlusSMARTpool Human GLI1 (L-003896-00-005, Dharmacon), ON-Target PlusSMARTpool Human CD44 siRNA (L-009999-00-0005, Dharmacon); ON-TARGETplus Non-targeting Pool (D-001810-10-05) served as a control. Transfection was performed with 4D-nucleofector AMAXA (Lonza) using 1.5 μg of siRNA/1 × 106 cells. Efficacy of transfection was verified after 48 h.
Oligonucleotides corresponding to Spp1 shRNA (5′-AGCTAGTCCTAGACCCTAA-3′ against rat Spp1, NM_012881.2) and control shRNA Neg (5′ GTCTCCACG CGCAGTACATTT-3′, based on pSilencer shNeg from Ambion) were cloned into a lentivector pLenti-U6-shRNA-Rsv(GFP-Puro) (GenTarget Inc, San Diego, USA). Rat C6 glioma cells (5 × 104) were seeded onto 24-well plates, transduced with 5 × 105 ready-to-use lenitiviral particles in 0.5 ml culture medium according to a manufacturer's protocol, and shSpp1 or shNeg clones were enriched by incubation with puromycin 2 μg/ml (BioShop, Canada Inc., Burlington). Efficacy of Spp1 gene silencing in heterogeneous pools was examined by qPCR and ELISA. For “rescue” experiments 6 × 104 C6 LVSpp1 cells were seeded on 24-wells plates and after 24 h cells were transfected with 18 ng/μl of plasmid DNA and a transfection reagent Viromer® RED (Lypocalyx, Germany). Twenty four hours after transfection cells were transferred to sphere culture medium and grown for 7 or 14 days.
In order to generate shRNA resistant constructs coding for a wild type and a ΔC-term pSpp1 (lacking a CD44 domain of Spp1), we performed a site-directed mutagenesis. We designed mismatched oligonucleotides binding to Spp1 shRNA binding site: Spp_mut_R: CTTCCTTACTCTTTGGATCGA GTACTAGTTTGTCC TCATGGCTGTG and Spp_mut_F: CCATGAGGACAAA CTAGTACT CGATCCAAAGAGTAAGGAAGATGAT AG. Primer-extension reaction amplified pEGFP-N1 vector carrying a wild type Spp1 cDNA (wtSpp1) or Spp1ΔC cDNA. The PCR reaction was performed with Phusion polymerase (New England Biolobs) using reaction conditions recommended by the manufacturer. Primer annealing was performed in 60°C. In order to eliminate template DNA, PCR product was digested with DpnI restriction enzyme and further transformed into XL1-Blue E.coli strain. Designed mutagenesis introduced point mutations without affecting aminoacid sequence and in the same time generated a new restriction site for SpeI enzyme. Simultaneous digestion with SpeI (Thermo Scientific) and EcoRI (Thermo Scientific) helped us to preselect proper clones before sequencing. The resulting plasmids were verified by sequencing.
Statistical significance was determined by Student's t-test; p values < 0.05 were considered significant. The results are expressed as a mean ± standard deviation from 3–5 independent experiments (different cell passages).
This work was supported by a grant 2012/04/A/NZ3/00630 from the Polish National Science Center (BK) and by INSERM (RP).
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