We previously identified CLEC14A as a tumour endothelial marker. Here we show that CLEC14A is a regulator of sprouting angiogenesis in vitro and in vivo. Using a human umbilical vein endothelial cell spheroid-sprouting assay, we found CLEC14A to be a regulator of sprout initiation. Analysis of endothelial sprouting in aortic ring and in vivo subcutaneous sponge assays from clec14a+/+ and clec14a−/− mice revealed defects in sprouting angiogenesis in CLEC14A-deficient animals. Tumour growth was retarded and vascularity reduced in clec14a−/− mice. Pull-down and co-immunoprecipitation experiments confirmed that MMRN2 binds to the extracellular region of CLEC14A. The CLEC14A-MMRN2 interaction was interrogated using mouse monoclonal antibodies. Monoclonal antibodies were screened for their ability to block this interaction. Clone C4, but not C2, blocked CLEC14A-MMRN2 binding. C4 antibody perturbed tube formation and endothelial sprouting in vitro and in vivo, with a similar phenotype to loss of CLEC14A. Significantly, tumour growth was impaired in C4-treated animals and vascular density was also reduced in the C4-treated group. We conclude that CLEC14A-MMRN2 binding has a role in inducing sprouting angiogenesis during tumour growth, which has the potential to be manipulated in future antiangiogenic therapy design.
It is well established that solid tumour growth relies on the recruitment of endothelial cells and ultimately blood vessels from the surrounding healthy tissue. These recruited blood vessels deliver oxygen and nutrients, through blood flow, to the tumour. A primary mechanism of this recruitment is through sprouting angiogenesis of vessels adjacent to the tumour arising from tumour-derived release of vascular endothelial growth factor (VEGF). Sprouting angiogenesis proceeds by initial formation of a tip cell from a resting endothelial cell. The tip cell then migrates away from the existing vessel leaving dividing stalk cells behind it and creating the new sprout. Sprouting angiogenesis is a tightly regulated process, where the main regulatory components are VEGFR2, Notch and Angiopoietin/Tie2 signalling pathways with cross-talk been these systems essential for direction, growth and cell specification.1, 2 However, recent studies have highlighted the role of multiple other pathways as regulators of this process, including factors involved in glycolysis3 and PKA (protein kinase A) signalling,4 as well as new regulators of extracellular matrix composition.5, 6 Manipulation of these factors has also been shown to suppress angiogenic sprouting in vitro and in vivo.
Targeting angiogenesis in cancer has many therapeutic advantages, including efficient delivery to target tissue type, stable genetic profile and lower potential for side effects than conventional chemotherapy. Current antiangiogenic therapies in the clinic primarily target the VEGF signalling pathway, but with limited success.7 More recent efforts to develop effective antiangiogenic therapies have focussed on understanding and targeting the endothelial tip and stalk cells during sprouting angiogenesis.2 For this to be effective, greater knowledge is required to understand the pathways involved in tip cell formation and behaviour.
CLEC14A is a single-pass transmembrane glycoprotein that belongs to the vascular expressed C-type lectin family 14, whose other members include CD248/TEM1/endosialin, thrombomodulin and CD93.8 Although functionally CLEC14A is relatively unstudied, available data suggest that manipulation of CLEC14A levels or function-blocking antibodies will regulate endothelial migration possibly through an interaction with the extracellular matrix.9, 10, 11, 12 CLEC14A was originally identified to be an endothelial-specific gene that is highly upregulated on vessels associated with multiple solid tumours.9 More recent work has shown CLEC14A as part of a ‘common angiogenesis signature’ in a meta-analysis of 121 head and neck squamous cell carcinomas, 959 breast cancers and 170 clear-cell renal cell carcinomas.13 MMRN2, an endothelial-specific member of the emilin family and component of the extracellular matrix,14, 15 was recently found as an extracellular-interacting protein for CLEC14A, and MMRN2 and CLEC14A were both upregulated in tumour vasculature during tumour progression.11 Thus, although it is becoming apparent that CLEC14A has a likely function in the tumour vasculature, our knowledge is restricted. In this study, we have investigated CLEC14A in sprouting angiogenesis and for the first time examined its role in vivo.
CLEC14A regulates sprouting angiogenesis in vitro
We previously described a role for CLEC14A in endothelial migration and tube formation in vitro.9 To investigate the role of CLEC14A in sprouting angiogenesis in vitro, human umbilical vein endothelial cell (HUVEC) spheroids were generated from HUVECs treated with small interfering RNAs (siRNAs) targeting clec14a or a non-complementary siRNA duplex. Knockdown of clec14a expression was confirmed at the mRNA level by quantitative PCR (qPCR) for both clec14a-targeted siRNAs with an average reduction of 84 and 83% across three experiments (Figure 1a) and at the protein level by western blot analysis of protein extracts probed with an anti-CLEC14A polyclonal antisera (Figure 1b). VEGF-induced sprouting from CLEC14A knockdown spheroids was impaired; knockdown spheroids produced on average 6.9 or 6.4 sprouts per spheroid for duplex 1 or 2, respectively, compared with 13.2 for control cells (Figures 1c and d). To determine the role of CLEC14A in tip/stalk cell formation, control HUVECs and knockdown HUVECs were stained either red or green and mixed, before spheroid formation and induced sprouting (Figure 1e). Knockdown of CLEC14A reduced the percentage of cells at the tip position (33%) compared with control cells (67%); however, there was no effect on the percentage of stalk cells that were derived from CLEC14A knockdown HUVECs (Figure 1f). These data suggest that CLEC14A has a role in sprout initiation and migration.
CLEC14A regulates sprouting angiogenesis in vivo
Previously published data for CLEC14A has demonstrated its role in endothelial biology in vitro; however, its in vivo role has not been reported. To investigate the role of CLEC14A in vivo and ex vivo, mice were generated to replace the clec14a coding sequence (CDS) with a lacZ reporter (Figure 2a). Breeding was normal (Supplementary Table 1). Aortas were isolated from clec14a+/+ and clec14a−/− mice. Extracted cDNA was analysed by qPCR and confirmed the loss of the clec14a coding region, but the expression of the 5′- and 3′-untranslated regions (UTRs) were retained (Figure 2b) and the expression of mmrn2 was unaltered (Supplementary Figure 1). Loss of CLEC14A at the protein level was also confirmed by western blot analysis of lung tissue lysates (Figure 2c).
To confirm the role of CLEC14A in sprouting angiogenesis in a multicellular three-dimensional coculture, aortas were isolated, cut into rings and embedded in collagen. Cellular outgrowth was stimulated by VEGF and monitored over 7 days before end-point quantitation of endothelial sprouting. Again, loss of CLEC14A impaired endothelial sprout outgrowth and migration (Figure 2d). Aortic rings from wild-type mice produced over double the number of tubes compared with that observed for CLEC14A knockout (KO) mice (30.6 tubes compared with 13.4 tubes, respectively) (Figure 2e). In addition, the maximum migration, which is defined by the furthest distance migrated away from each aortic ring, was also reduced in KO cultures (Figure 2f). To assess whether CLEC14A has a similar function in vivo, sponge barrels were implanted subcutaneously into CLEC14A KO mice. Cellular infiltration and neoangiogenesis were stimulated using basic fibroblast growth factor injections into the sponge every 2 days for 2 weeks. Macroscopic analysis of sponge sections stained with haematoxylin and eosin revealed impaired infiltration of cells into the sponge in clec14a−/− animals (Figures 2g and h). In addition, vascularity was significantly reduced (P<0.01) for clec14a−/− animals (Figure 2i). To confirm that the endothelial cells lining the neoangiogenic vessels express clec14a in this model, sponges and livers from CLEC14A KO mice were stained with x-gal. Strong x-gal staining was observed on blood vessels within the sponge compared with matched liver sections (Figure 2j). From these data, we can conclude that mouse CLEC14A expression regulates endothelial migration and angiogenic sprouting in vivo, as well as in vitro, and CLEC14A is upregulated on sprouting endothelium.
CLEC14A promotes tumour growth
CLEC14A expression is found highly upregulated on human tumour vessels compared with vessels from healthy tissue, suggesting that cancer therapies could be targeted against CLEC14A.9 Therefore, to investigate whether loss of CLEC14A affects tumour growth, we used the syngeneic Lewis lung carcinoma (LLC) model. For this, 1 × 106 LLC cells were injected subcutaneously into the right flank of either clec14a+/+ or clec14a−/− mice. Tumour growth was impaired in the clec14a−/− mice compared with clec14a+/+ littermates (Figure 3a). This was confirmed by three independent experiments. Excised tumours taken from clec14a−/− mice were smaller in size (Figure 3b) and smaller in weight (Figure 3c) than clec14a+/+ littermates. To determine whether the vascular density within these tumours was also affected, tissue sections were stained with an anti-CD31 antibody. The analysis shows a reduced density of discrete vessels (Figures 3d and e) and reduced percentage endothelial coverage (Figure 3f). In healthy tissues, highest expression of x-gal in sections from clec14a−/− mice was seen in the liver vessels (black arrow), but was vastly less than that seen on both mature vessels with erythrocyte-filled lumens (Figure 3g, black arrows) and immature microvessels within the tumour (Figure 3g, red arrows), confirming that clec14a is upregulated on tumour vessels.
Identification and confirmation of CLEC14A-MMRN2 interaction
To identify potential binding partners for the extracellular domain for CLEC14A, we first purified CLEC14A extracellular domain protein tagged with human Fc. This protein or Fc alone was incubated with HUVEC whole-cell lysates and precipitated using protein A agarose beads. The precipitated proteins were then washed and separated on a sodium dodecyl sulphate–polyacrylamide gel electrophoresis (SDS–PAGE). Seven gel regions were excised, digested and analysed by mass spectrometry. The most abundant protein identified was MMRN2 with 12 peptides (11 unique), and no peptides in the corresponding control pull-down fraction. Western blot analysis of the precipitates confirmed the presence of MMRN2 in the CLEC14A-ECD-Fc pulldown and was not detected in the Fc-alone pulldown (Figure 4a). To further confirm this interaction, endogenous CLEC14A was immunoprecipitated from HUVEC whole-cell lysates. Western blot analysis confirmed MMRN2 co-precipitation in the CLEC14A precipitate but was not detected in the immunoglobulin G (IgG) control (Figure 4b).
Development and validation of CLEC14A monoclonal antibodies
To further our understanding of CLEC14A, we next produced cross-species-reactive antibodies. To enable this, murine CLEC14A protein with a human Fc tag was expressed in HEK293T cells and purified on a protein A column. Mice were then immunised with 50 μg mCLEC14A with complete Freund’s adjuvant to break tolerance. Clones were screened for activity against human CLEC14A or human Fc. To confirm that the clones could recognise cell-bound CLEC14A, HEK293T cells overexpressing HA-CLEC14A were stained with clone C2 or C4 or a monoclonal HA tag antibody. FACS (fluorescence-activated cell sorter) analysis shows increased fluorescence for each of the antibodies in the HA-CLEC14A-overexpressing cells compared with control-transfected cells (Figure 5a). To confirm that antibodies recognise the endogenous form of CLEC14A, these clones were used to stain HUVEC treated with control or clec14a-targeted siRNAs. Control HUVECs were stained strongly by clone C2 and C4 and this staining was reduced to isotype control levels by knockdown of CLEC14A (Figure 5b). These results confirmed the specificity of the CLEC14A monoclonal antibodies.
To determine whether the C2 and C4 clones bind to the same region of CLEC14A, HUVECs were pretreated with bovine serum albumin, C2 or C4 antibody before C2-FITC (fluorescein isothiocyanate) staining. C2 incubation blocked C2-FITC staining effectively, but C4 had little effect (Figure 5c). The same pretreatment was repeated before C4-FITC staining. C2 antibody did not affect C4-FITC staining; however, HUVECs pretreated with C4 showed reduced binding of C4-FITC (Figure 5d). From these results we can conclude that C2 and C4 bind to discrete regions of CLEC14A.
A CLEC14A monoclonal antibody blocks CLEC14A-MMRN2 binding
To determine whether either of these CLEC14A monoclonal antibodies could inhibit the binding of MMRN2 to CLEC14A, CLEC14A-ECD-Fc was preincubated with increasing concentrations of mIgG1, or C2, or C4, before incubation with lysates from HEK293T cells overexpressing MMRN2. Precipitates were then separated and probed for MMRN2 or CLEC14A-ECD-Fc. MMRN2 binding was observed for CLEC14A-ECD-Fc precipitates blocked with mIgG1 or C2 (Figure 5e) but no MMRN2 binding was observed in the C4-blocked precipitates (Figure 5f). This confirms that the C4, but not the C2, monoclonal antibody blocks MMRN2 binding to CLEC14A.
CLEC14A-MMRN2-blocking antibody inhibits tube formation and sprouting angiogenesis in vitro and in vivo
We previously showed that CLEC14A expression regulates endothelial cell migration and tube formation.9 To assess whether C2 or C4 have a role in modulating endothelial cell migration, wounds were scratched into HUVEC monolayers and treated with 20 μg/ml mIgG1, C2 or C4. Wound closure was assessed at 16–24 h. However, no difference was observed between any of the treatments (data not shown). Antibody treatment also had no effect on CLEC14A expression (Supplementary Figure 2). To determine whether the CLEC14A monoclonal antibodies have regulatory properties in in vitro tube formation, HUVECs were plated onto Matrigel and treated with either mIgG1, C2 or C4 for 16 h. The C2 treatment had no effect on tube formation compared with the mIgG1 control; however, C4 treatment affected branching and meshes (Figure 6a). The number of meshes (Figure 6b) was decreased in the C4 treatment group, with a corresponding increase in the number of branches (Figure 6c) for this treatment group compared with the control and C2 groups. Furthermore, C4-treated HUVECs have decreased branch length (Figure 6d). These data suggest that C4 inhibits the sprouting or sensing and delays interconnectivity of the tubes, but the second CLEC14A-targeted antibody (C2) was without activity on tube formation.
To investigate how disruption of the MMRN2-CLEC14A interaction affects sprouting in vitro, we treated HUVEC spheroids with 20 μg/ml C4 or C2 or mIgG1 control antibodies. Control, mIgG1-treated, spheroids formed sprouts after 16 h, as expected (Figure 6e). C2 treatment had no effect on sprouting, but C4 treatment inhibited sprout formation by 50% (Figures 6e and f). To further investigate, aortic ring cultures were also supplemented with 20 μg/ml C4 or C2 or mIgG1 antibodies. Endothelial outgrowth and tube formation was well established after 7 days culture in the presence of mIgG1 (Figure 6g). C4 antibody effectively inhibited tube outgrowth; however, C2 antibody was inactive in regulating tube/sprout formation from aortic rings (Figures 6g and h).
To confirm the importance of MMRN2, HUVECs were treated with mmrn2-targeted siRNA or a control siRNA duplex. Knockdown of mmrn2 expression was confirmed by qPCR (Figure 6i). Endothelial sprouting from MMRN2 knockdown HUVEC spheroids formed 8.9 (duplex 1) or 8.6 (duplex 2) sprouts per spheroid, compared with 15.7 for control spheroids (Figure 6j).
To evaluate the role of the MMRN2-CLEC14A interaction in vivo, subcutaneous sponge implants were used. Sponge infiltration was stimulated as previously described with the addition of either 10 μg mIgG1 or C4 antibody. Total cellular sponge infiltration was significantly reduced (P<0.01) in the C4 treatment group compared with the mIgG1 controls (Figures 6k and l). Vascular density of the invaded sponge was also reduced for the C4 antibody group (Figure 6m). These data demonstrate that the MMRN2-CLEC14A interaction promotes in vivo angiogenesis.
CLEC14A-MMRN2-blocking antibody inhibits tumour growth
As CLEC14A expression is most abundant on tumour endothelial cells and CLEC14A expression is associated with MMRN2 in tumours,11 we hypothesised that disruption of this interaction would perturb tumour growth. Therefore, mice with LLC tumours were injected intraperitoneally two times per week with 10 μg C4 or mIgG1 (control) for the duration of the experiment. Tumour growth was slowed for mice treated with C4 antibody compared with the control, mIgG1, treatment group (Figure 7a). Tumours from the C4-treated mice were smaller in size (Figure 7b) and weight (Figure 7c) than control animals. Again, we examined the vascular density within these tumours. Tissue sections were stained with an anti-CD31 antibody and fluorescent analysis revealed a reduced density of discrete vessels (Figures 7d and e) and the percentage endothelial coverage (Figure 7f). This suggests that CLEC14A binding to MMRN2 is an important functional component of tumour-induced angiogenesis.
CLEC14A is one of a small group of endothelial genes that contribute to tumour angiogenesis in multiple tumour types.9, 13 Here we demonstrate that through the loss of CLEC14A, tumour growth is inhibited in vivo (Figure 3). A similar phenotype has also been observed for other tumour endothelial markers, such as TEM8,16 endoglin,17 galectin,18 ELTD113 and endosialin;19 this demonstrates the importance of these tumour endothelial-expressed genes in vascularisation and tumour growth. Although many groups have focused on factors involved in physiological sprouting angiogenesis, these tumour endothelial-expressed genes could deliver tumour antiangiogenic therapeutic potential.20
Upregulation of CLEC14A has been observed in human tumours9, 13, 21 and murine models of pancreatic and cervical cancer,11 which supports our findings that clec14a expression is upregulated on tumour vessels in the LLC model (Figure 3). CLEC14A has been shown to regulate multiple aspects of endothelial biology including adhesion,10, 12 migration9, 10, 12 and tube formation,9, 10, 11 and we now demonstrate that, as we first predicted,22 it is also important for sprouting angiogenesis in vitro and in vivo (Figures 1 and 2). We can infer that this role of CLEC14A is through endothelial–endothelial interactions or endothelial–extracellular matrix interactions, because in vitro HUVEC sprouting is perturbed by CLEC14A knockdown, suggesting that the presence of other cell types is dispensable. We also observed for the first time the upregulation of clec14a expression on neoangiogenic vessels in the subcutaneous sponge assay (Figure 2). This is expected as newly formed endothelial sprouts have been modelled to experience extremely low shear stress (0.2 Pa) from the 4.2 μm of the bifurcation point to the tip of the sprout,23 and clec14a expression is known to be upregulated by low shear stress.9 Therefore, it is possible that CLEC14A has a role in regulating physiological sprouting angiogenesis also; however, its role will likely be limited by the coexpression of MMRN2.
Zanivan et al.11 identified MMRN2 as a component of the extracellular matrix that interacts with CLEC14A. We independently verified this interaction through pulldown of proteins from HUVEC lysates using the extracellular domain of CLEC14A, as well as co-immunoprecipitation of the endogenous proteins (Figure 4). Through the generation and validation of CLEC14A monoclonal antibodies, we identified two antibodies that bind to discrete regions of CLEC14A (Figures 5c and d) and have shown that the C4 but not the C2 clone blocks the interaction of CLEC14A with MMRN2 (Figures 5e and f). To probe the function of the CLEC14A-MMRN2 interaction, we used the C4 antibody in Matrigel tube-forming assays and found an increase in branching and decrease in evolved meshes (Figure 6). Knockdown by siRNA or targeting with polyclonal CLEC14A antisera has a similar effect on branching in this in vitro Matrigel assay.9 However, another monoclonal antibody that binds CLEC14A but does not block MMRN2 binding had no effect (Figure 6). In a study using phage display to develop IgGs targeting the c-type lectin domain of CLEC14A, some of the generated IgGs reduced HUVEC cell migration and tube formation, although not all of the clones were tested.12 As our monoclonal antibody has a similar function, it is possible that the MMRN2 binding site is within the c-type lectin domain region of CLEC14A, although further work is required to confirm this. In vitro and in vivo sprouting assays treated with C4 antibodies also demonstrated the role of the CLEC14A-MMRN2 interaction for endothelial sprouting (Figure 6). Lorenzon et al.24 previously observed antiangiogenic activity with soluble MMRN2 protein. These data support our model, as soluble MMRN2 protein could be binding to CLEC14A and disrupting the interaction of CLEC14A with MMRN2 in the extracellular matrix (Figure 8). Finally, we found that the CLEC14A-MMRN2 interaction is important for tumour growth (Figure 7), and C4 treatment recapitulated tumour growth and reduced tumour vascularity as seen in clec14a−/− mice (Figure 3). Antibody inhibition of tumour endothelial marker function has been suggested as a mode of antiangiogenic therapy for TEM8,25 and our studies corroborate this approach. However, in this example no ligand or mode of activity was identified. This is the first time that CLEC14A and a specific extracellular interaction has been shown to be important for tumour growth, and suggests a hitherto unknown avenue into new antiangiogenic therapies.
Materials and methods
For western blotting and immunoprecipitation, the following antibodies were used: primary antibodies—sheep polyclonal anti-human CLEC14A (R&D Systems, Abingdon, UK), mouse monoclonal anti-human tubulin (Sigma, Dorset, UK) and mouse polyclonal anti-human MMRN2 (Abnova, Taoyuan City, Taiwan); secondary antibodies—goat polyclonal anti-mouse IgG conjugated to horseradish peroxidase (Dako, Cambridge, UK) and donkey polyclonal anti-sheep IgG conjugated to horseradish peroxidase (R&D Systems). For immunofluorescence, the antibodies used were: primary antibodies—rabbit polyclonal anti-murine PECAM (Santa Cruz, Heidelberg, Germany); secondary antibodies—donkey polyclonal anti-rabbit conjugated to Alexa Fluor 488 (Invitrogen, Paisley, UK). For flow cytometry, the antibodies used were: primary antibodies—mouse monoclonal anti-HA tag (CRUK, Cambridge, UK) and mouse monoclonal anti-CLEC14A (C2, C4 described below); secondary antibodies—goat polyclonal anti-mouse IgG conjugated to Alexa Fluor 488 (Invitrogen).
For protein production, lentiviral plasmids psPAX2 (lentiviral packaging; Addgene, Cambridge, MA, USA), pMD2G (envelope plasmid; Addgene) and pWPI hCLEC14A-ECD-Fc (lentiviral mammalian expression plasmid containing IRES-EGFP; Addgene) were used. pWPI hCLEC14A-Fc and mCLEC14A-Fc was generated by initial PCR subcloning from clec14a IMAGE clone (Origene, Rockville, MD, USA) into pcDNA3-Fc plasmid. The primers used were as follows: human CLEC14A fwd, 5′-IndexTermTAGTAGGAATTCGAGAGAATGAGGCCGGCGTTCGCCCTG-3′; human CLEC14A rev, 5′-IndexTermAGAACCGCGGCCGCTGGAGGAGTCGAAAGCCTGAGGAGT-3′; murine CLEC14A fwd, 5′-IndexTermTAGTAGGAATTCGAGAGAATGAGGCCAGCGCTTGCCCTG-3′; murine CLEC14A rev, 5′-IndexTermCTACTAGCGGCCGCTCGTGGAAGAGGTGTCGAAAGT-3′. EcoR1 and Not1 restriction sites were used to insert CLEC14A. A further round of PCR subcloning was performed to transfer the CLEC14A-Fc fusion into pWPI. The primers used were as follows: human CLEC14A fwd, 5′-IndexTermTAGTAGTTAATTAAGAGAGAATGAGGCCGGCGTTC-3′; murine CLEC14A fwd, 5′-IndexTermTAGTAGTTAATTAAGAGAGAATGAGGCCAGCGCTT-3′; human Fc rev, 5′-IndexTermCTACTAGTTTAAACTCATTTACCCGGAGACAGGGA-3′. For this step, Pac1 and Pme1 restriction sites were used.
MMRN2 mammalian expression plasmid was constructed by PCR cloning from mmrn2 IMAGE clone (Thermo, Loughborough, UK) into pHL-Avitag3,26 using the following primers: fwd, 5′-IndexTermCCGGACCGGTCAGGCTTCCAGTACTAGCC-3′; rev, 5′-IndexTermCGGGGTACCGGTCTTAAACATCAGGAAGC-3′. Age1 and Kpn1 restriction enzymes were used.
HUVECs were isolated as described previously.9 Umbilical cords were obtained from Birmingham Women’s Health Care NHS Trust with informed consent. HUVECs and HEK293T cells were cultured as described previously.27
SiRNA transfections in HUVECs were performed as previously described for clec14a.9 For mmrn2, predesigned siRNA duplexes were used (Ambion silencer select: ID S36387 and S36388). Lentivirus was produced in HEK293T cells by transient transfection with the lentiviral packaging, envelope and expression plasmids above. Plasmids were incubated in OptiMEM (Invitrogen) with polyethylenimine (36 μg/ml) at a ratio of 1:4 for 10 min at room temperature before adding to HEK293T cells in cDMEM (Dulbecco’s modified Eagle’s medium containing 10% bovine calf serum). Media supernatant was used to transduce fresh HEK293T cells. GFP-positive HEK293T cells were sorted and used for protein production. Expression of MMRN2 in HEK293T cells was achieved by polyethylenimine transient transfection as above using pHL-Avitag3 hMMRN2.
cDNA was prepared using the High-Capacity cDNA Archive Kit (Applied Biosystems) from 1 μg of extracted total RNA. qPCR reactions were performed with Express qPCR supermix (Invitrogen) on an RG-3000 (Corbett, Manchester, UK) thermocycler. Primers for human clec14a and flotillin2 were as described previously.9 Primers for murine clec14a 5′-UTR, CDS, 3′-UTR and murine β-actin are as follows: 5′-UTR fwd, IndexTermTTCCTTTTCCAGGGTTTGTG; 5′-UTR rev, IndexTermGCCTACAAGGTGGCTTGAAT; CDS fwd, 5′-IndexTermAAGCTGTGCTCCTGCTCTTG-3′; CDS rev, 5′-IndexTermTCCTGAGTGCACTGTGAGATG-3′; 3′-UTR, IndexTermCTGTAGAGGGCGGTGACTTT; 3′-UTR rev, IndexTermAGCTGCTCCCAAGTCCTCT; murine β-actin fwd, 5′-IndexTermCTAAGGCCAACCGTGAAAAG-3′; murine β-actin rev, 5′-IndexTermACCAGAGGCATACAGGGACA-3′. Relative expression ratios were calculated according to the efficiency-adjusted mathematical model.28
Western blotting and immunoprecipitation
Whole-cell protein lysates were made and co-immunoprecipitation experiments were performed as described previously,29 but protein was extracted from 2 × 107 HUVECs. For initial isolation of CLEC14A-interacting proteins, 5 μg of CLEC14A-Fc or an equimolar amount of hFc was used. For endogenous immunoprecipitation experiments, 0.4 μg of anti-CLEC14A antibody or sheep IgG was used. For blocking experiments, 5 μg of CLEC14A-Fc or hFc were bound to protein G beads overnight in phosphate-buffered saline (PBS). Beads were blocked for 5–6 h in PBS containing 20% foetal calf serum (PAA, Linz, Austria). Bound CLEC14A-Fc or hFc protein was blocked with increasing concentrations of mIgG, C2 or C4 in binding buffer overnight. Lysates from MMRN2-transfected HEK293T cells were then incubated overnight with the bead complexes before washing and analysing by western blot. Standard protocols were used for western blotting and SDS–PAGE.
Cells were detached with cell dissociation buffer (Invitrogen) and then rinsed in PBS before incubation in the blocking buffer (PBS, 3% bovine serum albumin, 1% NaN3) for 15 min. Subsequent staining was carried out using 10 μg/ml anti-HA tag (CRUK) and 10 μg/ml anti-CLEC14A (C2 and C4 described below), as primary antibodies, in the blocking buffer for 30 min. Cells were rinsed in PBS and stained with goat polyclonal anti-mouse IgG conjugated to Alexa Fluor 488 (Invitrogen) in the blocking buffer. Data (15 000 events per sample) were collected using a FACSCalibur apparatus (Becton Dickinson, Oxford, UK), and results were analysed with Becton Dickinson Cell Quest software (Oxford, UK).
HUVEC spheroid-sprouting assay and in vitro Matrigel tube-forming assay
Generation of HUVEC spheroids and induction of endothelial sprouting in a collagen gel was performed as described previously,30 using 1000 HUVECs per spheroid. Quantification was performed 16 h after embedding. To quantify sprout growth, the number of sprouts was counted, and the cumulative sprout length and the maximal sprout length was assessed. For two-colour sprouting experiments, HUVECs were prelabelled with orange and green CellTracker dyes (Invitrogen). After 24 h, spheroids were fixed in 4% formaldehyde and mounted with Vectorshield (Vector labs, Peterborough, UK). Slides were imaged with an Axioskop2 microscope and AxioVision SE64 Rel4.8 software (Zeiss, Cambridge, UK).
For the Matrigel tube-forming assays, 1.4 × 105 HUVECs were seeded onto 70 μl basement membrane extract (Matrigel; BD Bioscience, Oxford, UK) in a 12-well plate. After 16 h, images were taken of five fields of view per well using a Leica DM IL microscope (Leica, Milton Keynes, UK) with a USB 2.0 2M Xli digital camera (XL Imaging LLC, Carrollton, TX, USA) at × 10 magnification. Images were analysed with the Angiogenesis analyser plugin for Image J (Carpentier G, et al. Angiogenesis analyzer for ImageJ. 4th ImageJ User and Developer Conference Proceedings) and available at the NIH website (http://imagej.nih.gov/ij/macros/toolsets/Angiogenesis%20Analyzer.txt).
Culture media from CLEC14A-Fc-expressing HEK293T cells was collected. Culture media was flowed over a HiTrap protein A HP column (GE Healthcare, Amersham, UK) and protein was eluted using a 0–100% gradient of 100 mM sodium citrate (pH 3) before neutralising with 1 M Tris base. Fractions were run on an SDS–PAGE and assessed for protein purity and specificity by Coomassie staining and western blotting. Fractions containing similar concentrations of protein were combined and dialysed in PBS before functional assays.
Monoclonal antibody generation
Mouse monoclonal antibodies were commercially prepared by Serotec Ltd (Oxford, UK) using the following protocol to break tolerance supplied by us. Purified mouse CLEC14A-Fc fusion protein was given at 50 μg in Freunds complete adjuvant subcutaneously. Two weeks later, mice were given another 50 μg subcutaneously, but this time in Freunds adjuvant. Mice were culled and spleens harvested for fusion 2 weeks later.
Generation of clec14a−/− mice
Mice were housed at the Birmingham Biomedical Services Unit (Birmingham, UK). C57BL/6N VGB6 feeder-dependent embryonic stem cells containing the CLEC14A deletion cassette (Clec14atm1(KOMP)Vlcg; project ID VG10554) were procured from the Knockout Mouse Project (University of California, Davis, Davis, CA, USA). The Transgenic Mouse Facility at the University of Birmingham generated chimeric mice by injection of embryonic stem cells into albino C57BL/6 mice and were bred to C57BL/6 females to generate mice heterozygous for the cassette. Animal maintenance had appropriate Home Office approval and licensing.
Aortic ring and murine subcutaneous sponge angiogenesis assay
Aortas were isolated and processed for aortic ring assays in collagen as described previously.31 Tube/sprout outgrowth, maximal endothelial migration and total endothelial outgrowth was quantitated. The murine subcutaneous sponge angiogenesis assay was performed as described previously,32 with slight modification. Male C57 black mice were implanted with a subcutaneous sterile polyether sponge disc (10 × 5 × 5 mm3) under the dorsal skin of each flank at day 0. One hundred microlitres of basic fibroblast growth factor (40 ng/ml; R&D Systems) was injected through the skin directly into the sponges every other day for 14 days. Sponges were excised on day 14, fixed in 10% formalin and paraffin embedded. Sections were stained with haematoxylin and eosin, sponge cross-sections were taken using a Leica MZ 16 microscope (Leica, Milton Keynes, UK) with a USB 2.0 2M Xli digital camera at × 1 magnification for cellular invasion analysis. Images captured by Leica DM E microscope (Leica, Milton Keynes, UK) at × 40 magnification were analysed for vessel density. Vessel counts were assessed in five fields per section per sponge. All animal experimentation was carried out in accordance with Home Office License number PPL 40/3339 held by RB.
Tumour implantation assays
A total of 106 LLCs were injected subcutaneously into the flank of male mice at 8–10 weeks of age. Tumour growth was monitored by daily calliper measurements, and after 2—4 weeks growth, tumour mass was determined by weight, fixed in 4% paraformaldehyde, paraffin embedded and serial sections cut at 6 μm.
Immunofluorescence and X-gal staining.
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We thank Dr Laurens van der Flier, Somantix and Dr Raj Mehta, Cancer Research Technology, for helpful discussions. PN was funded by Cancer Research UK (CRUK, grant number C4719/A6766 to RB). The Portuguese Fundacao para a Ciencia e tecnologia funded AV. XZ was funded by a knowledge transfer partnership (KTP007696) from the Technology Strategy Board. PL is funded by MRC and the University of Birmingham, and KK is funded by the University of Birmingham. The University of Birmingham Transgenic Mouse Facility is part of the MRC Centre for Immune Regulation.
RB and XZ are named inventors of a patent filed by Cancer Research UK in the United States Patent and trademark Office on 3 September 2009 under No. 61/ 239,584, bearing Attorney Docket No. P0357.70004US00 and entitled ‘Inhibitors’. All the other authors declare no conflict of interest.
Supplementary Information accompanies this paper on the Oncogene website
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Noy, P., Lodhia, P., Khan, K. et al. Blocking CLEC14A-MMRN2 binding inhibits sprouting angiogenesis and tumour growth. Oncogene 34, 5821–5831 (2015). https://doi.org/10.1038/onc.2015.34
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