Notch1 signaling in NOTCH1-mutated mantle cell lymphoma depends on Delta-Like ligand 4 and is a potential target for specific antibody therapy
NOTCH1 gene mutations in mantle cell lymphoma (MCL) have been described in about 5–10% of cases and are associated with significantly shorter survival rates. The present study aimed to investigate the biological impact of this mutation in MCL and its potential as a therapeutic target.
Activation of Notch1 signaling upon ligand-stimulation and inhibitory effects of the monoclonal anti-Notch1 antibody OMP-52M51 in NOTCH1-mutated and -unmutated MCL cells were assessed by Western Blot and gene expression profiling. Effects of OMP-52M51 treatment on tumor cell migration and tumor angiogenesis were evaluated with chemotaxis and HUVEC tube formation assays. The expression of Delta-like ligand 4 (DLL4) in MCL lymph nodes was analyzed by immunofluorescence staining and confocal microscopy. A MCL mouse model was used to assess the activity of OMP-52M51 in vivo.
Notch1 expression can be effectively stimulated in NOTCH1-mutated Mino cells by DLL4, whereas in the NOTCH1-unmutated cell line JeKo-1, less effect was observed upon any ligand-stimulation. DLL4 was expressed by histiocytes in both, NOTCH1-mutated and –unmutated MCL lymph nodes. Treatment of NOTCH1-mutated MCL cells with the monoclonal anti-Notch1 antibody OMP-52M51 effectively prevented DLL4-dependent activation of Notch1 and suppressed the induction of numerous direct Notch target genes involved in lymphoid biology, lymphomagenesis and disease progression. Importantly, in lymph nodes from primary MCL cases with NOTCH1/2 mutations, we detected an upregulation of the same gene sets as observed in DLL4-stimulated Mino cells. Furthermore, DLL4 stimulation of NOTCH1-mutated Mino cells enhanced tumor cell migration and angiogenesis, which could be abolished by treatment with OMP-52M51. Importantly, the effects observed were specific for NOTCH1-mutated cells as they did not occur in the NOTCH1-wt cell line JeKo-1. Finally, we confirmed the potential activity of OMP-52M51 to inhibit DLL4-induced Notch1-Signaling in vivo in a xenograft mouse model of MCL.
DLL4 effectively stimulates Notch1 signaling in NOTCH1-mutated MCL and is expressed by the microenvironment in MCL lymph nodes. Our results indicate that specific inhibition of the Notch1-ligand-receptor interaction might provide a therapeutic alternative for a subset of MCL patients.
KeywordsMantle cell lymphoma Notch1 Delta-like ligand Angiogenesis OMP-52 M51
Acute lymphoblastic leukemia
American Type Culture Collection
Delta like ligands
Fetal bovine serum
False discovery rate
Gene Expression Omnibus
Gene Set Enrichment analysis
Mantle cell lymphoma
NOTCH1 Intracellular domain
NOD Scid Gamma
Phosphate buffered saline
Robust Multichip Analysis
Although with current standard therapy high initial response rates can be achieved, early relapses and rapid disease progression determine the clinical course of most mantle cell lymphoma (MCL) patients . In the last years, new therapies were approved targeting the proteasome, the PI3K-Akt-mTOR pathway, the B-cell receptor (BCR) signaling pathway and the anti-apoptotic Bcl-2 protein family. Yet, MCL remains an incurable disease . The t (11;14)(q13;q32) translocation leading to Cyclin D1 overexpression is the primary oncogenic event in MCL pathogenesis . Furthermore, constitutive activation of BCR signaling plays an important role in disease development . Additionally, genomic profiling revealed a high number of secondary genetic alterations and recurrent mutations affecting cell cycle, DNA damage response and apoptosis pathways that contribute to pathogenesis and aggressiveness of MCL . Among them, NOTCH1 gene mutations have been described with a frequency of 5–10% and were shown to be associated with shorter survival rates [5, 6]. Therefore, further investigation of the biological effect of this mutation in MCL and its potential as a therapeutic target is of great interest.
The majority of the previously described NOTCH1-mutations in MCL consist of either small frameshift-causing indels or nonsense mutations in exon 34 . These mutations lead to truncation of the C-terminal PEST-domain, thereby removing the recognition site from the ubiquitin ligase degradation complex, resulting in a more stable and transcriptionally active form of Notch1-intracellular domain (NICD). The Notch signaling pathway operates in a context- and tissue-dependent way participating in diverse cellular processes, such as cancer stem cell biology, angiogenesis, cell proliferation and survival . In addition to the well-known Notch target genes HES1 and HEY1, two basic-helix-loop-helix (Bhlh)-class of transcription factors, numerous genes have been identified as directly regulated by activated Notch1 . Some cancer-related target genes of Notch include NF-κB family members, CYCLIN D1, p21, GATA3, MYC and DTX1 . In mammals, Notch signaling is usually activated upon interactions with Delta-like ligands (DLL1, DLL3, DLL4) and Jagged ligands (JAG1, JAG2), resulting in a series of proteolytic cleavage events that finally release NICD from its membrane receptor and lead to its nuclear translocation .
Targeting Notch signaling has been studied in various cancer types and particularly using gamma-secretase inhibitors (GSI) in hematological malignancies [6, 10, 11]. However, the clinical applicability of GSI is limited as it can cause severe diarrhea resulting from simultaneous inhibition of Notch1 and Notch2 signaling in gut epithelial stem cells [12, 13]. Thus, alternative strategies for therapeutic targeting of Notch1 are highly warranted. Recently, antibodies that inhibit signaling of both, wild-type and mutated Notch1 receptors have been characterized . OMP-52M51 (brontictuzumab) is a full length IgG2 humanized monoclonal antibody that selectively binds the negative regulatory region of the Notch1 receptor leading to inhibition of Notch1 signaling . A phase I study has been conducted in subjects with solid tumors showing efficacy in cases with Notch1 pathway activation  . In this study, we investigated the role of the Notch ligands in activating Notch1 signaling in NOTCH1-mutated and - unmutated MCL cell lines and evaluated the effects of OMP-52M51 in these cell lines.
Cell lines and primary MCL cells
MCL cell lines Mino (CRL-3000), JeKo-1 (CRL-3006) and REC-1 (CRL-3004), were obtained from American Type Culture Collection (ATCC). To avoid Mycoplasma contamination, cell lines were routinely tested for Mycoplasma infection by PCR. The identity of all cell lines was verified by using GenePrint® kit (Promega, Madison, WI, USA). MCL cell lines were cultured in RPMI 1640 complemented with 10–20% fetal bovine serum (FBS), 2 mM L-glutamine and 50 μg/mL penicillin/streptomycin (Life Technologies, Carlsbad, CA, USA) and grown in a humidified atmosphere at 37 °C with 5% CO2. The murine bone-marrow derived stromal cell line OP9 (CRL-2749; ATCC) overexpressing DLL4 (OP9-DLL4) was generated and grown as described [17, 18]. Primary cells from MCL patients were isolated and cultured as described  and conserved within the Hematopathology collection of our institution registered at the Biobank from Hospital Clínic-IDIBAPS (R121004–094). The ethical approval for this project including informed patient consent was granted following guidelines of the Hospital Clínic Ethics Committee.
Ligand stimulation and cell treatment
Four micrograms per milliliter of the recombinant Notch-receptor-ligands DLL1, DLL4, JAG1 and JAG2 (R&D Systems, Minneapolis, MN, USA) were resuspended in phosphate buffered saline (PBS) and stored in culture plates for 4 h at 4 °C to let them attach to the plates. MCL cells were treated with 25 μg/mL of OMP-52M51 or human IgG2 (both kindly provided by Oncomed Pharmaceuticals, Redwood City, CA, USA) and incubated at 37 °C for 2 h prior to adding them to the ligand-coated plates for stimulation. For coculture experiments, OP9 cells were plated overnight, and then medium was replaced by MCL cells (0.5 × 106 cells/mL) previously treated for 2 h with OMP-52M51. After 24 h of coculture, MCL cells were collected by carefully rinsing the wells without disturbing the stroma monolayer and processed as required.
Whole-cell protein extracts were obtained using Triton containing lysis buffer (Tris-HCl pH 7.6 20 mmol/L, NaCl 150 mmol/L, EDTA 1 mmol/L, 1% Triton X-100) supplemented with protease and phosphatase inhibitors (10 μg/mL leupeptin, 10 μg/mL aprotinin, 1 mmol/L phenylmethanesulfonyl fluoride, 5 mmol/L NaF, 2 mmol/L Na3VO4). Solubilized proteins were quantified by Bradford protein assay and 50 μg of protein was analyzed by Western Blotting. The following primary antibodies were used: cleaved-NOTCH1 (Val1744)(D3B8), MEK1/2, phospho-MEK1/2 (Ser217/221)(41G9) (Cell Signaling, Boston, MA, USA), ERK1 (K-23), phospho-ERK (Thy202/204) (E-4) (Santa Cruz, Dallas, TX, USA), α-tubulin and β-actin (Sigma Aldrich, Saint Louis, MI, USA). Chemiluminescence was detected with ECL substrate (Pierce Biotechnology Waltham, MA, USA) on a mini-LAS4000 Fujifilm device (Fujifilm, Valhalla, NY, USA). Protein expression was densitometrically quantified using the Image Gauge software (Fujifilm).
Immunohistochemistry and confocal microscopy
Lymph node (LN) biopsies from MCL cases were obtained from the Hematopathology collection of our institution registered at the Biobank from Hospital Clínic-IDIBAPS (R121004–094). Formalin-fixed paraffin-embedded (FFPE) tissue slides (serial 8 μm sections) were dewaxed and tissue antigens were retrieved by boiling for 10–15 min in sodium citrate (10 mM, pH 6.0). Slides were allowed to cool down to room temperature (RT) and then washed in distilled water and PBS. Quenching was carried out using 1% H2O2 in 100% methanol (40 min, RT) and permeabilization with 0,3% Triton-X-100 (20 min, Sigma-Aldrich) in PBS. Sections were incubated overnight with anti-human DLL4 (H-70) (Santa Cruz) and anti-human CD68 (Dako, Glostrup, Germany). Background staining was determined by incubating with irrelevant antibodies. Unspecific fluorescence was quenched by incubating with avidin/biotin blocking solutions (Vector Lab, Burlingame, CA, USA). For DLL4 detection, tissue slides were incubated with anti-rabbit IgG-HRP antibody (Dako). Signal was amplified using the Cyanine-3 Tyramide Signal Amplification Kit (TSA; NEL 744, Perkin Elmer, Waltham, MA). For CD68 detection, a biotinylated anti-mouse IgG (Vector Lab) was added following incubation with avidin/biotin complex (Elite Vectastain ABC Complex kit, Vector Lab). Signal was developed by adding Alexa-488-conjugated streptavidin. Nuclei were stained with Topro-3 (Invitrogen, Carlsbad, CA, USA) and mounted with Fluoromount-G (Southern Biotech., Birmingham, AL, USA). Images were acquired using a LSM510 laser scan confocal microscope (Zeiss, Oberkochen, Germany) coupled to an Axiovert200 (Zeiss) microscope, using 63x Plan-Neofluar magnification.
Cell cycle assay
A total of 3 × 105 MCL cells were collected after stimulation with DLL4 and incubated with OMP-52M51 for 48 h. Then cells were fixed in ice-cold 70% ethanol while being gently vortexed, incubated at − 20 °C for 24 h, washed in PBS and resuspended in 500 μL of staining solution containing 20 μg/mL propidium iodide (Invitrogen) and 100 μg/mL RNase A (Thermofisher) in PBS. Cells were incubated during 30 min at 37 °C and analysed using BD LSRFortessa 4 L cytometer (Becton Dickinson, Franklin Lakes, NJ, USA). Cell cycle analysis was performed using FlowJo software (Becton Dickinson).
MCL cells were stimulated with DLL4 and incubated with OMP-52M51 for 48 h. Transwell culture polycarbonate inserts (6.5 mm diameter, 8 μm of pore size) (Corning, NY, USA) were transferred to wells containing 600 μL of RPMI supplemented with 0.5% BSA with 200 ng/mL of human recombinant CXCL12 (Peprotech). One hundred microliter of cell suspension (0.5 x 106cells) was then added into the transwell inserts. Input cell count was obtained from adding 100 μL of cell suspension to wells containing 600 μL of 0.5% BSA in RPMI 1640. After 3 h, 100 μL were collected in triplicates from each lower chamber and input well, viable cells were counted on an Attune cytometer (Thermofisher, Waltham, MA, USA) under constant flow rate. Migration is represented as the ratio between migrated cells and total viable input cells.
Human umbilical vein endothelial cells (HUVEC) tube formation assay
HUVEC, kindly provided by Dr. MC Cid (IDIBAPS), were cultured as described . Supernatants from MCL cells (1 × 106 cells/mL) were collected after 48 h of OMP-52M51 treatment of DLL4-stimulated cells. 24-well plates were coated with 300 μL of Matrigel (Becton Dickinson) before 500 μL of HUVEC (0.5 × 105 cells/mL] and 500 μL of the supernatants were added. After 24 h, number of branch points was quantified as a measure of in vitro angiogenesis as the mean of five randomly chosen fields from each well. Images were taken with a DM IL LED microscope coupled to a DFC295 camera (magnification 100x) with Leica Application Suite v 3.7 software (Leica, Wetzlar, Germany).
Gene expression profiling
Total RNA was extracted using the TRIzol method (Life technologies) according to manufacturer’s instructions. RNA integrity was examined with the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA) and only high quality RNA samples were further processed. RNA from MCL cell lines was hybridized to a Gene Chip HT HG-U219 array, according to Affymetrix (Santa Clara, CA, USA) standard protocols. RNA from MCL lymph nodes was hybridized to a Gene Chip Human Genome U133 plus 2.0 arrays, according to Affymetrix standard protocols. Determination of the detection call for each probe set of the array was obtained with GeneChip® Command Console® Software (AGCC) (Affymetrix). Raw data was normalized using the Robust Multichip Analysis (RMA) algorithm of the BioConductor Affy Package. Differential expression data analysis was carried out using the Multiexperiment Viewer Platform (TM4-MEV) . The number of statistically significant up- and down-regulated genes was determined using Rank Products methodology  for cell lines, and Volcano plot  for MCL lymph nodes, both setting up a false discovery rate (FDR) < 0.2 and an absolute fold change (FC) > 1.75. PANTHER (http://pantherdb.org/) was used to perform gene ontology (GO) pathways analysis  to visualize the relationships between the significantly modulated genes of NOTCH-mutated MCL lymph nodes and proteins in known pathways of biological processes . Primary microarray data of MCL cell lines and primary MCL lymph nodes are available at the Gene Expression Omnibus (GEO) of the National Center for Biotechnology Information under accession Nos. GSE125349, GSE36000 and GSE46969.
Gene set enrichment analysis (GSEA)
For GSEA, the desktop application version 2.0 (GSEA, Broad Institute at MIT, Cambridge, MA; http://www.broadinstitute.org/gsea/) was applied using experimentally derived custom genes. The “Custom MCL” gene set was designed by manually grouping gene sets involved in pathways of Notch-activated genes in MCL according to the results described by Ryan et al. . Briefly, we searched molecular signatures (http://software.broadinstitute.org/gsea/msigdb/) corresponding to the pathways described in the GO canonical pathways analysis and GSEA analysis of transcripts increased by Notch in Mino cells (except MYC), and the significant genes were grouped into specific pathways (Additional file 1: Table S1). The “NOTCH1 direct targets” gene set was also constructed based on the 79 genes described by Ryan et al. . Similarly, the “NOTCH1 custom” gene set was designed by manually selecting significant Notch1 related genes found in the literature [6, 11, 15, 27, 28, 29, 30]. Two-class analysis with 1000 permutations of gene sets and a weighted metric was used for all cases. The resulting gene sets with a false discovery rate (FDR) < 0.05 were considered to be significant, except for the “NOTCH1” gene set, where a FDR < 0.12 was used. GSEA analysis was performed of MCL cell lines stimulated or not with DLL4 and treated or not with OMP-52M51 and of MCL lymph node tissues with or without mutations in a NOTCH gene. HeatMaps were created using the Morpheus software (https://software.broadinstitute.org/morpheus/) followed by hierarchical clustering using one minus Pearson correlation of the average of gene expression in order to illustrate the differential expression of those genes significantly modulated by DLL4 stimulation and OMP-52M51 treatment in the MCL cell lines and by NOTCH gene mutation in MCL lymph node tissues for the all custom gene sets analysis performed.
In vivo mouse model
NSG (NOD-scid-gamma) mice were injected intravenously (i.v.) with 10 × 106 Mino cells. MCL cell engraftment was periodically monitored over a 3 months period. After 3 months, mice presented infiltration in several organs. Tumor cells from lymph nodes were collected, cultured in RPMI 1640 + 10% FBS as described above and cryopreserved after several passages. We next confirmed that these Mino cells engraft faster in a secondary transplant (45–60 days). Again, these cells obtained from lymph nodes were collected and cryopreserved. These “fast engrafting” tumor cells were then thawed and expanded to get enough cells for in vivo studies. 225 × 106 Mino cells were then stimulated ex vivo by coculturing them with OP9-DLL4 cells (7.5 × 106 Mino cells/plate 100 × 20 mm2 (Corning). After 24 h of incubation, 15 × 106 stimulated Mino cells were injected into the intraperitoneal cavity (IC) of 12 female NSG mice at the age of 10 weeks. Mice were treated intraperitoneally 1 day prior to injection of cells and then every 4 days with 20 mg/kg of OMP-52M51 or control antibody human IgG2 (6 mice/group). After 10 days, mice were sacrificed and a peritoneal lavage (PL) was done by injecting the cavity with 5 mL of cold PBS. Human B-cells were purified by using human CD19 beads. Protein extracts were obtained and expression of cleaved Notch1 was analyzed by Western Blot. Procedures involving animals and their care are conforming to institutional guidelines that comply with national and international laws and policies (EEC Council Directive 86/609, OJ L 358, 12 December, 1987) and were authorized by the local ethical committee.
Data is represented as the mean ± SD of 3 independent experiments. All statistical analyses were done by using GraphPad Prism 6.01 software (GraphPad Software, La Jolla, CA, USA). Volcano plot of P values as a function of weighted FC for mRNA was performed by using Multiplot Studio v1.5.20 software (Benooist-Mathis Lab, Harvard Medical School, MA, USA). Comparisons between 2 groups of samples were analyzed with Kruskall-Wallis nonparametric test followed by Mann-Whitney U test. Results were considered statistically significant when P < 0.05 (*P < 0.05; **P < 0.01; ***P < 0.001).
Activation of Notch1 signaling can effectively be achieved by stimulation with DLL4 in NOTCH1-mutated MCL cells
A NOTCH1-mutation affecting the PEST-domain in exon 34 (p.Q2487*) was described in the established MCL cell line Mino [5, 6]. The effect of this mutation is considered to be ligand-dependent. In contrast, the MCL cell line REC-1 presented an intragenic deletion in exon 28 encoding for a truncated Notch1 protein with increased activity in a ligand-independent fashion [26, 31].
Treatment of NOTCH1-mutated MCL cells with OMP-52M51 effectively prevents DLL4-dependent activation of Notch1
We next investigated the effect of the humanized monoclonal Notch1 antibody OMP-52M51 in NOTCH1-mutated (Mino) and unmutated (JeKo-1) MCL cell lines. Since the recognition-binding site of OMP-52M51 in the EGF-like domain is missing in the REC-1 cell line due a deletion in this site , this cell line was not suitable for further investigation.
To evaluate the effect of OMP-52M51 on downstream signaling of Notch1, we performed a gene expression profile analysis in JeKo-1 and Mino cells stimulated with DLL4 and treated with OMP-52M51 for 48 h. Using the GSEA software analyzing a customized NOTCH1 set of genes (NOTCH1 custom) [6, 11, 15, 27, 28, 29, 30], we detected 44 significantly upregulated leading edge genes (Fig. 2c, Additional file 2: Table S2) upon DLL4-treatment in Mino cells (FDR < 0,123; p < 0,005, NES > 1.48). As displayed in the Z score heatmap, the significantly modulated genes upon DLL4 stimulation in Mino cells were effectively downregulated by treatment with OMP-52M51 (Fig. 2c).
When we applied a signature of NOTCH1 target genes described in MCL cells (NOTCH1 direct targets) , a strong upregulation of these genes was detected in Mino cells stimulated with DLL4 (FDR < 0.001; p < 0.001, NES = 3.00). A good correlation was also observed in JeKo-1 stimulated with DLL4 (FDR = 0.025; p = 0.025, NES = 1.40) (Additional file 3: Table S3 and Figure S1), confirming again that in NOTCH1-unmutated cells the activation of Notch signaling is less potent than in mutated cells. This may be due to the fact that the signaling would not be sustained enough as the wild type Notch1 protein has a rapid turnover . Again, OMP-52M51 was able to revert the expression of these direct Notch-target genes in Mino cells (Fig. 2d).
OMP-52M51 significantly impedes DLL4-induced upregulation of genes involved in lymphoid biology, lymphomagenesis and disease progression
Next, we analyzed the gene expression profile of lymph nodes from primary MCL cases (n = 21), 3 of them harboring NOTCH1/2 mutations. By using the same GSEA analysis, in lymph nodes from primary MCL cases with NOTCH1/2 mutations, we detected an upregulation of the same gene sets as observed in DLL4-stimulated Mino cells (Fig. 3b, Additional file 5: Table S5). In these cases, to maintain Notch signaling, a crosstalk between tumor MCL cells and accessory cells, probably histiocytes, is required. In addition, the PANTHER GO analysis of the 55 genes differentially expressed in MCL lymph nodes carrying NOTCH gene mutations compared to NOTCH-unmutated MCL lymph nodes, filtered by Volcano plot (Fig. 3c, Additional file 6: Table S6), revealed 818 signaling pathways associated with leukocyte biology primarily enriched for biological processes associated with disease progression such as regulation of tethering/rolling, adhesion and migration of leukocytes (Fig. 3d).
We next studied the effect of aberrant Notch1 signaling on cell migration by means of chemotaxis assays. As shown in Fig. 4c, DLL4 stimulation of Notch1 significantly increased CXCL12-induced migratory capacity of Mino cells that could be abrogated by treatment with OMP-52M51. In contrast, no effect could be observed in unmutated JeKo-1 cells (Fig. 4c).
The DLL4-Notch1 signaling pathway plays an important role in regulating blood vessel formation during physiological and pathological angiogenesis [33, 34]. Furthermore, data from our gene expression arrays revealed that DLL4 stimulation induces several genes related to angiogenesis. This prompted us to investigate the impact of activating NOTCH1 mutations on tumor angiogenesis. We therefore used supernatants of Mino and JeKo-1 cells stimulated or not with DLL4 and treated or not with OMP-52M51 in a tube formation assay with HUVEC. Supernatants of DLL4 stimulated NOTCH1-mutated Mino cells significantly increased number of branch points as a measure of in vitro angiogenesis compared to those of unstimulated cells. Importantly, the proangiogenic effect of these supernatants could be effectively abolished by treatment of cells with OMP-52M51. Again, no differences were detected in unmutated JeKo-1 cells (Fig. 4d).
OMP-52 M51 effectively inhibits DLL4 induced activation of Notch1 in an in vivo model
Activating NOTCH1 mutations are among the most frequent secondary genetic alterations in MCL detected in 5–10% of cases [5, 6, 35]. Similar to CLL, the majority of NOTCH1 alterations described in MCL are nonsense truncating mutations and small frame-shift indels located in exon 34 which encodes the PEST domain, resulting in enhanced Notch1 signaling [7, 30]. The clinical significance of this mutation is highlighted by the fact that patients harboring a NOTCH1-mutation had significantly shorter overall survival rates [5, 6]. Yet, the molecular impact of NOTCH1 mutations in MCL is not well understood. Recently, it has been postulated that Notch signaling regulates genes involved in BCR and cytokine signaling as well as the oncogene MYC, which sustains proliferation of Notch-dependent MCL cell lines . Targeting Notch signaling has been studied in various cancer types [6, 10, 36], and particularly in hematological malignancies carrying NOTCH1 mutations [10, 37]. It has been reported that GSI-mediated inhibition of Notch signaling in NOTCH1-mutated MCL cells resulted in reduction of cell proliferation and apoptosis induction . However, the clinical applicability of GSI is limited due to severe gastrointestinal toxicities [12, 13]. Thus, alternative strategies for targeting Notch signaling are highly warranted. In this way, we analyzed the effect of a humanized IgG2 monoclonal antibody OMP-52M51 that showed encouraging antitumor efficacy in T-acute lymphoblastic leukemia (ALL) xenograft models . Recently, phenotypic and molecular features of resistance after long-term treatment with OMP-52M51 have been reported, that are highly heterogeneous, suggesting that leukemia cells can adopt several strategies to evade Notch inhibition according to the therapeutic drug used .
In Non-Hodgkin lymphomas, only little is known about the dependency of Notch1 signaling activation upon a certain ligand. Candidate cellular sources include other hematopoietic cells; endothelial cells, which are capable of inducing Notch signaling in B lymphoma cells  and DLL1/4-expressing fibroblastic cells in secondary lymphoid organs . In this study, we show for the first time that DLL4 is a potent ligand to activate Notch1 signaling in MCL cells harboring a NOTCH1 mutation in the PEST domain, whereas JAG1 and JAG2 could not sufficiently stimulate Notch1 activity. DLL4 was shown to be constitutively expressed in some lymphoid organs, where it influences regulation of Notch signaling during hematopoiesis . In T-ALL cells, where mutations in NOTCH1 are frequent and well characterized, DLL4 plays an important role as part of the tumor microenvironment contributing to early steps of T-ALL cell growth . Although immobilized DLL1 was also used to model ligand-dependent Notch1 activation in MCL , the effect of DLL1 in MCL cells is lower than of DLL4. Only a minor effect upon any ligand stimulation was observed in NOTCH1-wt cells corroborating the fact that NOTCH1 mutations in the PEST domain lead to a more stabilized protein due to loss of the recognition site from the ubiquitin ligase degradation complex . Furthermore, we provide evidence that DLL4 is expressed in the lymph node MCL compartment, where it could promote Notch activation. In particular, we detected DLL4 to be highly expressed in the vascular endothelium and by some CD68-positive cells, indicating that DLL4 expressed by the LN microenvironment might provide a specific niche for Notch activation.
Furthermore, our results confirm that stimulation of Notch signaling by Delta-like ligands could have a critical role in MCL pathogenesis as we observed upregulation of several direct Notch target genes  involved in angiogenesis, apoptosis, migration and adhesion, cell cycle, cytokine signaling, DNA damage and repair, MTOR and MAPK signaling, leukocyte proliferation and defense response of B cell activation, cell cycle progression and oncogenesis both in DLL4-stimulated Mino cells and in lymph nodes from primary MCL cases carrying NOTCH mutations. In this way, we detected the induction of transcription factors genes implicated in B-cell differentiation and activation, PAX5 and IRF8 [43, 44, 45, 46] as well as of MYBL2, a transcription factor participating in cell cycle progression [47, 48] and recently described as a direct Notch1 target in B cell lymphomas . We confirmed a possible interaction between Notch and BCR signaling in B cell malignancies  as we observed the upregulation of several genes related to B cell activation (FYN, FGR, NEDD9 and SH2B2) and an increase of cell proliferation after DLL4 stimulation in NOTCH1-mutated MCL cells. Moreover, the results obtained for NOTCH -mutated MCL lymph nodes could be considered a proof-of-concept for those observed in DLL4-stimulated Mino cells, and are in concordance with the poor overall survival  and prognosis  associated with NOTCH mutations in MCL. Our next aim was to analyze the potential effect of the anti-Notch1 antibody OMP-52M51 on blocking the Delta-like ligand-induced signal in MCL. Treatment of Mino cells with OMP-52M51 could effectively inhibit DLL4-dependent Notch1-activation and suppress transcriptional expression of several direct Notch target genes described in MCL . These findings are in line with results observed in T-ALL, where OMP-52M51 treatment of T-ALL patient samples harboring mutations in the NOTCH1-PEST-domain caused strong inhibitory effects on the expression of Notch-target genes . Furthermore, we confirmed that in our model anti-Notch1 therapy attenuated the expression levels of the four well known Notch-target genes that have been described as a marker of the effect of OMP-52M51 in T-ALL (CR2, DTX1, HES1 and HES4) . Moreover, we elucidated a functional relationship between Notch1 signaling and microenvironment processes related to MCL aggressiveness such as cell proliferation, cell migration and angiogenesis. Notch1 signaling has been shown to play a role in CCL19-driven homing of CLL cells  and Notch1 signaling inhibition in multiple myeloma was described to prevent tumor cell migration . Accordingly, we showed that OMP-52M51 reverts the strong induction of gene signatures related to tumor cell migration and adhesion upon Notch1 activation and prevents DLL4-stimulated migratory capacity of MCL cells.
The DLL4-Notch1 axis is known to play an important role in regulating angiogenesis. Previous studies have shown that productive tumor angiogenesis requires cooperation between VEGF-A, which induces proliferation of endothelial ‘tip’ cells and expression of DLL4 in ‘stalk’ cells . In this context, DLL4 inhibits endothelial proliferation and promotes branching morphogenesis, and the balance between proliferation and branching is key to the formation of a functional capillary network. As such, treatment with anti-DLL4 antibodies resulted in disorganized angiogenesis, characterized by endothelial proliferation without formation of functional capillaries . In line with this, we showed that supernatants of NOTCH1-mutated MCL cells stimulated with DLL4 increased HUVEC tube formation, whereas OMP-52M51 blocked this proangiogenic effect. We therefore postulate that by promoting pronounced vasculature development, DLL4-stimulated Notch1 signaling might contribute to the clinically observed aggressive behavior of NOTCH1-mutated MCL. Interestingly, NRARP, one of the genes with the strongest induction upon Notch1 stimulation in our gene expression array, has been described to be related to Notch signaling  and shown to act as a molecular link between Notch and Wnt signaling in endothelial cells to control stability of new vessel connections . In this sense, our results suggest that in MCL, the link between Notch1 and NRARP might promote angiogenesis and needs to be further explored.
Importantly, we showed that even if DLL4 could potentially activate Notch1 signaling irrespective of the mutational status of NOTCH1, its functional effects are specific for NOTCH1-mutated MCL cells. This might be due to the fact that in NOTCH1-unmutated MCL, the weak expression of intracellular cleaved Notch1 upon ligand-activation seems to be very unstable due to rapid proteasomal degradation and might not be potent enough to cause functionally relevant transcriptional effects. This observation is of clinical relevance as a specific Notch1-antibody therapy might be a promising therapeutic alternative for the subgroup of patients with NOTCH1-PEST-mutations.
We show for the first time that DLL4 is a potent stimulator of Notch1 signaling in NOTCH1-mutated MCL and that expression of this ligand observed in histiocytic cells from MCL lymph nodes might provide a specific niche for Notch activation. We propose a link between Notch1-induced expression of tumor-promoting genes and activation of processes contributing to a more aggressive MCL phenotype. Furthermore, our findings indicate that specific inhibition of the Notch1-ligand-receptor interaction provides an efficient and specific therapeutic alternative for a subset of MCL patients.
The authors thank Jocabed Roldan and the Genomics Unit of IDIBAPS for their technical support.
Conception and design: ES, MLG, DC. Development of methodology and performance of research: ES, FA, BCS, SXT, MH, AG, VR, PF. Acquisition and management of samples: ES, FA, BCS, SXT, MH, SB, AG, VR, PF. Analysis and interpretation of data: ES, FA, PV, MLT, MLG, DC; Writing of manuscript: ES, MLG, DC. Review of manuscript: SXT, WRA, SB, MLT, EC, FA. Study supervision: MLG, DC. All authors read and approved the final manuscript.
The study was supported by research funding from the Spanish Ministry of Economy and Competitiveness through the Plan Estatal de Investigación Científica y Técnica y de Innovación [MINECO], SAF15–67633-R and RTI2018–094584-B-I00 [to DC], SAF2016–75442-R [to MLT] and was cofunded by the European Regional Development Fund [ERDF] and the CERCA program from Generalitat de Catalunya, Centro de Investigación Biomédica en Cáncer [CIBERONC] [CB16/12/00334 and CB16/12/00225] and Generalitat de Catalunya Suport Grups de Recerca [2017 SGR 1009] and the Robert-Bosch-Foundation.
Ethics approval and consent to participate
Primary cells from MCL patients conserved within the Hematopathology collection of our institution registered at the Biobank from Hospital Clínic-IDIBAPS (R121004–094). The ethical approval for this project including informed patient consent was granted following guidelines of the Hospital Clínic Ethics Committee.
Procedures involving animals and their care are conforming to institutional guidelines that comply with national and international laws and policies (EEC Council Directive 86/609, OJ L 358, 12 December, 1987) and were authorized by the local ethical committee.
Consent for publication
The authors declare that they have no competing interests.
- 38.Agnusdei V, Minuzzo S, Pinazza M, et al. Dissecting molecular mechanisms of resistance to Notch1-targeted therapy in T-cell acute lymphoblastic leukemia xenografts. Haematologica. 2019. https://doi.org/10.3324/haematol.2019.217687 [Epub ahead of print].
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