Abstract
The adhesion receptors of the integrin family play an essential role during tumour progression and thus represent interesting potential targets for the development of new therapeutic agents. The snake venom contains natural inhibitors of integrin–ligand interactions called disintegrins. It also contains C-type lectin proteins mainly known as modulators of platelet aggregation. In this study, we demonstrate that lebectin, a novel C-type lectin isolated from Macrovipera lebetina venom, displayed an anti-integrin activity. Lebectin inhibited the integrin-mediated attachment of various tumour cell lines to different adhesion substrata. The C-type lectin also completely blocked cell migration towards fibronectin in haptotaxis assays and prevented invasion of fibrin gels by tumour cells. In addition, lebectin proved to be a potent inhibitor of tumour cell proliferation. Although the specific integrins affected by lebectin are not identified in this study, the integrin α5β1 might be involved.
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Main
The acquisition of cell motility and the capacity to invade basement membranes and adjacent tissues plays a central role in the complex multistep process of metastasis. Cell migration results in dynamic interactions between the cell, the extracellular matrix (ECM) and the cytoskeleton. These interactions are partly mediated by integrins, a family of cell surface adhesion receptors composed by the noncovalent association of α and β subunits.1 Integrins connect the ECM proteins outside to the actin cytoskeleton within the cell, allowing the traction required for cell migration.2, 3 In addition to regulating cell adhesion, integrins relay molecular cues regarding the cellular environment that influence cell shape, survival, proliferation and gene transcription. Integrins therefore play a pivotal role during tumour progression (for reviews, see [Parise et al4 and Hood and Cheresh5]).
C-type lectin proteins (CLPs) are a family of snake venom proteins that are structurally homologous to the carbohydrate recognition domain of animal C-type lectins. CLPs are 30 kDa proteins consisting of the association of two subunits. In spite of their highly conserved primary structure (40–70% similarity), CLPs are characterized by very distinct biological activities (see Marcinikiewicz6, Wang et al7 and references therein). For example, several CLPs inhibit von Willebrand factor (vWF) binding to the GPIb/IX complex, thus impeding platelet agglutination, whereas alboaggregins activate the GPIb complex, causing platelet agglutination. Other CLPs exhibit anticoagulant activities by binding to vWF or to the coagulation factors IX and/or X, while convulxin induces platelet aggregation by activating the collagen receptor GPVI (for a review, see Andrews and Berndt8).
Besides the action on platelet aggregation, it has recently been reported that venom CLPs, such as EMS16 from Echis multisquamatus,6 or bilinexin from Agkistrodon bilineatus9 have an anti-α2β1 integrin activity. In the case of aggretin from Calloselasma rhodostoma, recent studies gave rise to conflicting results concerning its interaction with α2β1 integrin.10, 11, 12, 13, 14 However, the targeting of CLPs might not be restricted to the α2β1 integrin, as we recently showed that lebecetin, isolated from Macrovipera lebetina venom, inhibits platelet aggregation15 and adhesion of tumour cells to various ECM ligands.16
In this work, we report a novel CLP, termed lebectin, also from M. lebetina venom that inhibits various integrin-mediated functions in tumour cells, including adhesion, proliferation and cell migration.
Materials and methods
Reagents
Venom was collected from M. lebetina snake in the serpentarium of Institut Pasteur, Tunis. Fast protein liquid chromatography (FPLC) column and Sephadex G75 were purchased from Amersham-Pharmacia and high-performance liquid chromatography (HPLC) column was obtained from Beckman. Dulbecco's modified Eagle's medium (DMEM) was purchased from GIBCO (Cergy-Pontoise, France) and foetal calf serum (FCS) from BioWhittaker (Fontenay-sous-Bois, France). Human fibrinogen, human laminin and poly-L-lysine were from Sigma (St Louis, MO, USA). Rat type I collagen was from Upstate (Lake Placid, NY, USA) and human fibronectin from Chemicon (Temecula, CA, USA). Human vitronectin was purified according to Yatogho et al.17 The 5–bromo-2′–deoxyuridine (BrdU) kit was from Boehringer (Mannheim, Germany).
Purification and N-terminal Amino-Acid Sequence of Lebectin
M. lebetina crude venom (267 mg) was dissolved in 0.2 M ammonium acetate, pH 6.8 and fractionated by a Sephadex G75 column equilibrated with the same buffer. The fractions from peak II were loaded onto a MonoS HR5/5 column pre-equilibrated with 50 mM HEPES pH 7.5. Elution was performed with a linear gradient of 0–1 M NaCl. Finally, resulting fractions were purified by reverse-phase HPLC on a C8 column (5 μm; 4.6 × 250 mm) equilibrated with 0.1% trifluoroacetic acid in 10% acetonitrile and then eluted at a flow rate of 1 ml/min with an acetonitrile linear gradient 10–80% over 60 min.
The homogeneity and apparent molecular mass of the purified lebectin and its subunits were determined by SDS-PAGE in 12.5% acrylamide gel under reducing or nonreducing conditions and confirmed by mass spectrometry analysis as previously described.15 The protein concentration was determined by the BCA protein assay (Pierce, Rochford, IL, USA).
The N-terminal amino-acid sequence of isolated native lebectin was determined as already described by using an Applied Biosystems 477A instrument. Sequence alignment was made by CLUSTAL X program.
Cell Adhesion Assay
The human fibrosarcoma (HT1080), melanoma (IGR39) and adenocarcinoma (HT29–D4) cell lines were routinely cultured in DMEM containing 10% FCS. Human leukaemia cells K562 were cultured in RPMI medium with 10% FCS.
Adhesion assays were performed as previously described.18, 19 Briefly, cells in single cell suspension were added to wells coated with purified ECM proteins and allowed to adhere to the substrata for 1 h (HT1080 and IGR39 cells) or 2 h (HT29–D4 and K562 cells) at 37°C. After washing, attached cells were stained by 0.1% crystal violet and lysed with 1% SDS. Absorbance was then measured at 600 nm. To test the dependency on divalent cations, adhesion was performed in Ca2+- and Mg2+-free Hanks' solution/0.2% borine serum albumin (BSA) (supplemented or not with 1 mM CaCl2 and 1 mM MgCl2) instead of adhesion buffer.
Cell Migration and Invasion Assays
In vitro cell migration assays were performed using modified Boyden chambers (NeuroProbe Inc, Bethesda, MD, USA) as previously described,18 except that incubation medium was DMEM/10% FCS. Cells were stained with 0.1% crystal violet and migration was quantified by measure of absorbance at 600 nm.
Tumour cell invasion of fibrin gels was carried out as described by Naito et al,20 except type I collagen (0.67 mg/ml) and lebectin (2–10 μg/ml) were incorporated to fibrinogen prior adding thrombin.
Cell Proliferation
IGR39, HT1080 and K562 cells were seeded at 15 000 cells/cm2 in the presence or absence of 10 μg/ml lebectin. Every day, IGR39 and HT1080 cells were quantified by crystal violet staining as for adhesion assay. K562 cells were enumerated by manual counting of an aliquot.
Proliferation was confirmed by BrdU incorporation into DNA of cells treated for 18 h at 37°C with 10 μg/ml lebectin. Nuclei of proliferating cells are stained by alkaline phosphatase activity using the detection kit according to the manufacturer's instructions. Images of cells were captured and analysed using a Leica DM IRBE microscope with cool Snap FX camera and the Metaview software (Princeton Instrument, Paris, France).
Results
Effect of Snake Venom on Tumour Cells Adhesion
To screen for venom peptides able to inhibit tumour cells integrins, we performed cell adhesion assays using a large array of purified ECM proteins. As illustrated in Figure 1a, attachment of the melanoma cell line IGR39 to fibrinogen, fibronectin and laminin-1 was completely abolished by venom from M. lebetina, while no effect could be observed on type I collagen. This is not restricted to melanoma cells, as adhesion of human tumour cells from ovarian (IGROV1) and colonic (HT29-D4) carcinomas was also affected (data not shown). The inhibition of attachment to fibrinogen of IGR39 (Figure 1b) and IGROV1 cells (not shown) was dosedependent. As illustrated in Figure 1c, IGR39 cells attached to immobilised proteins from venom and to fibrinogen with similar efficiencies. The effect of venom likely implicated the integrin family, as no inhibition was observed when using an integrin-independent substratum, such as poly-L-lysine (Figure 1a). Moreover, the attachment of IGR39 cells to immobilised proteins from venom was dependent on Ca2+/Mg2+ and was increased by Mn2+, two typical properties of integrin–ligand interactions (Figure 1d).
Purification and Characterisation of Lebectin
In order to isolate the proteins acting on tumour cells adhesion, crude venom from M. lebetina was first fractionated by Sephadex G75 gel filtration chromatography (Figure 2a). Proteins from peak II, which contained most of the antiaggregating activity on platelets, were then subjected to cation exchange chromatography on a Mono S column (Figure 2b). Peak P2S appeared to be composed of a single protein, as separation by reverse-phase HPLC gave only one peak (Figure 2c). It is a protein with an isoelectric point of 7.8 (data not shown). The purity of this protein, designated as lebectin, was confirmed by SDS-PAGE. Lebectin has a molecular mass of 30 kDa under nonreducing conditions and 16 kDa under reducing conditions (Figure 2c, inset). Moreover, mass spectroscopy analysis revealed a molecular mass of 30 468 Da for native lebectin and 16 158 Da upon treatment with a reducing agent (data not shown). This suggested that lebectin is composed of two 16 kDa subunits (either identical or with similar hydrophobicity) linked with disulphide bonds.
The N-terminal amino-acid sequence of the 39 first residues of lebectin confirmed that this protein is likely composed of two identical subunits and shows a relatively high degree of sequence identity with other known members of the CLP superfamily (Figure 3). The identity was higher with heterooligomeric CLPs, such as lebecetin, alboaggregin B, habu IX/X-bp or botrocetin, than with the homodimeric CLP LmsL.
Lebectin Affects Adhesion of Tumour Cells
Besides binding to platelet membrane proteins or blood coagulation factors, CLPs have recently demonstrated anti-integrin activity.6, 9, 10 In order to investigate the effect of lebectin on the behaviour of tumour cells, we first performed adhesion assays on a panel of purified ECM proteins by using various established human cell lines. As shown on Figure 4a, lebectin completely blocked the attachment of the melanoma cell line IGR39 to fibrinogen, fibronectin and laminin–1, while adhesion to vitronectin was only slightly decreased. The effect on attachment of K562 cells to fibronectin and IGR39 cells to fibrinogen (Figure 4b), fibronectin or laminin-1 (data not shown) was dosedependent. Lebectin also inhibited the adhesion of the fibrosarcoma cell line, HT1080 to fibrinogen and fibronectin (Figure 4c), but only partially affected that of the colonic HT29–D4 cells (Figure 4d). Whatever the cell line, lebectin did not affect the attachment to type I and IV collagens. Moreover, no inhibition could be observed with any cell line on the integrin-independent substratum, poly-L-lysine, suggesting that the effect of lebectin indeed involved the integrin family of adhesion receptors.
Lebectin Abolishes Tumour Cells Migration and Invasion
In order to colonise new organ sites, tumour cells have to access the lymphatic or blood vessel system, disseminate, extravasate and invade the new organ parenchyma. These events require cell adhesion, but also migration. We tested the ability of lebectin to inhibit integrin-dependent migration of HT1080 cells, using haptotaxis assays towards attractive proteins in modified Boyden chambers. As shown in Figure 5 25 μg/ml lebectin totally abolished HT1080 cells migration towards fibronectin (Figure 5a, upper panels). This inhibition was dosedependent with a partial effect at a concentration as low as 1 μg/ml (about 30 nM) (Figure 5b). Lebectin also affected migration of HT29-D4 and IGR39 cell lines (data not shown). However, as observed with cell adhesion, lebectin had not effect on migration of HT1080 cells towards type I collagen (Figure 5a, lower panels).
We next evaluated the effect of lebectin on tumour cell invasion using a previously described in vitro assay.20 Because HT1080 cells secrete large amounts of matrix metalloproteinases that rapidly hydrolyse fibrin gels,21 we therefore incorporated small amounts of collagen to perform invasion studies. As illustrated in Figure 6, lebectin at concentrations as low as 2 μg/ml (∼60 nM) completely blocked invasion of fibrin/collagen gels by HT1080 cells. In this assay, the venom peptide likely inhibited migration to fibrin, because invasion of collagen gels was unaffected (not shown).
Lebectin Inhibits Proliferation of Tumour Cells
It has long been known that most cell types require attachment to a substrate to be able to grow. As integrins are primarily responsible for cell adhesion to ECM, it is not surprising that they are involved in cell proliferation,22, 23 In order to know whether lebectin interferes with proliferation, we first followed the growth of IGR39, HT1080 and K562 cells in the absence or in the presence of the peptide. For all cell lines, the number of cells in the wells was dramatically reduced by the presence of 10 μg/ml (∼0.3 μM) lebectin in culture medium (Figure 7a). To confirm that the reduced cell number was really due to growth inhibition, HT1080 cells were cultured with lebectin for 18 h and proliferation was then visualised by detecting cells that have incorporated BrdU into DNA. As shown in Figure 7b, few nuclei exhibited uptake of BrdU in lebectin-treated cells when compared to control condition. Thus, lebectin clearly affected DNA synthesis and appears to be a potent inhibitor of tumour cell proliferation.
Discussion
The snake venom proteins are well-known modulators of platelet adhesion receptors and their ligands (reviewed in [Andrews and Berndt,8 Brand et al24]). Since their characterisation, snake disintegrins have been extensively studied. They specifically antagonise the integrin receptors and can thus prevent invasion of breast cancer cells and in vivo tumour progression.25 On the other hand, very little is known about the effect of venom CLPs on tumour cells behaviour. Here, we report the structural and biochemical characterisation of a new peptide, termed lebectin, isolated from the venom of the North Africa viper M. lebetina. Lebectin demonstrated a potent anti-integrin activity on various cancer cells.
Several lines of evidence suggest that lebectin is a member of the C-type lectins family. First, lebectin is composed of two 16 kDa subunits, a structure found in C-type lectins from snake venom.26, 27, 28 Second, lebectin was recognised (in enzyme-linked immunosorbent assay (ELISA), Western blot and immunoprecipitation assays) by an antibody raised against lebecetin, an already characterised C-type lectin from M. lebetina venom.15, 16 This suggests that, although lebecetin is an heterodimeric C-type lectin while lebectin is homodimeric, both proteins share some structural features. Third, the N-terminal amino-acid sequence shows a relatively high degree of sequence identity with other known members of the CLP superfamily. Curiously enough, the identity was higher with heterooligomeric CLPs such as lebecetin, alboaggregin B, habu IX/X-bp or botrocetin,15, 29, 30, 31 than with the homodimeric CLP LmsL.26 Determination of the entire amino-acid sequence of lebectin is in progress in order to confirm its homodimeric structure.
Until recently, the anti-integrin activity among snake venom proteins was considered to be characteristic for disintegrins. However, it has been reported that EMS16, a CLP from E. multisquamatus inhibits endothelial cells migration by interacting with α2β1 integrin.6 Here, we extend this initial observation to various established human tumour cells from diverse origin and to other integrin-dependent functions. Lebectin inhibits adhesion of melanoma, fibrosarcoma, adenocarcinoma and leukaemia cells to different integrin ligands. Moreover, cell attachment to immobilised lebectin is enhanced by Mn2+ and is divalent cationdependent (not shown), two typical properties of integrins, suggesting that lebectin affects cell adhesion by interacting with ECM receptors of the integrin family.
Cell migration requires the formation of new attachments at the leading edge and the release of attachments at trailing edge of the cell.32 Although the detailed mechanisms are not yet understood, it is clear that dynamic and reciprocal interactions between cell adhesion molecules, ECM and soluble factors are essential.5, 33, 34 Consequently, as primary receptors for ECM proteins, integrins are required for cell motility. Integrins also play a major role in cell invasion along with others protagonists, such as cadherins, matrix metalloproteinases or growth factors.35 The inhibitory effect of lebectin on cell migration and invasion is likely due to the reduced attachment to ECM proteins observed in the presence of the CLP. Indeed, both cell adhesion and migration are inhibited by lebectin in the case of fibronectin, whereas neither attachment nor migration to type I collagen are affected. In the same way, lebectin blocks adhesion to fibrinogen and invasion of three-dimensional matrices of fibrin, which derives from fibrinogen, but do not prevent invasion of collagen gels.
Lebectin also drastically decreases growth of melanoma, fibrosarcoma and leukaemia cell lines. Such an inhibition of tumour and endothelial cell growth has been reported for BJcuL, a CLP from the snake Bothrops jararacussu,36, 37 although this inhibition by BJcuL required higher concentrations. Because lebectin impairs cell adhesion, its antiproliferative effect might be an indirect one, as detachment of adherent cells may cause apoptosis. This is probably not the case for several reasons. First, in the proliferation test, cells are seeded in standard culture conditions. ECM proteins are those brought by FCS, that is, mainly vitronectin and fibronectin. As illustrated in Figure 4, adhesion to vitronectin is barely affected by lebectin. Moreover, cells did not detach from the substrate during the test and no cell debris could be observed. Furthermore, if the effect of lebectin on proliferation was due to cell detachment, the ratio of stained vs unstained nuclei should have been the same in the presence and in the absence of lebectin. This is clearly not the case, as shown in Figure 7b. Finally, the detachment cannot be taken into account in the case of K562 cells because these leukemia cells grow in suspension. The antiproliferative effect of lebectin is thus likely due to the impediment of integrin function, as reported in the case of function-blocking anti-integrin antibodies.23 However, whether the effect on integrins is direct (eg, physical association) or indirect (via a third partner) remains to be determined.
Recent reports have shown that CLPs may interact with the platelet integrin α2β1.6, 9, 10 However, the effect of CLPs on integrin function might not be as simple as suggested by initial observations. Thus, aggretin and trimucytin were first described as activating platelets by binding to α2β1 integrin,11, 12, 38, 39 but there is now evidence to suggest that these CLPs do not bind to α2β1 integrin.13, 14, 40 The fact that cell adhesion to collagens, which involves α2β1 integrins, is not affected by lebectin indicates that this integrin is probably not the target of lebectin. In addition, lebectin has not effect on migration towards type I collagen, a ligand of α2β1 integrin in HT1080 cells.41 The α2β1 integrin is likely not the only target of CLPs. It is possible that lebectin might act on several integrins because various different integrins mediate the adhesion of the tumour cells used in this study to fibrinogen, fibronectin and laminin–1. The integrin α5β1 may likely be involved, at least in some of the effects, because lebectin inhibited the adhesion and growth of the leukemia cell line K562 that only expresses this integrin at its cell surface.42 Moreover, the integrin α5β1 is expressed by both IGR39 and HT1080 cells.41 It is also worth pointing out, that HT29-D4 cells, that do not express α5β1 integrin,18, 43 are very little sensitive to lebectin. The identification of the specific integrin(s) involved in the effects of lebectin on tumour cells behaviour is currently under investigation.
In conclusion, we have isolated and characterised a novel homodimeric C-type lectin protein with a potent anti-integrin activity. Indeed, this venom-derived protein is able to prevent adhesion, migration, invasion and proliferation of tumour cells using in vitro assays. It could thus be interesting to check the effect of lebectin on in vivo tumorigenesis and metastasis development in animal models such as nude mouse or new born immunosuppressed rat.
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Acknowledgements
We thank Professor Koussay Dellagi (Institut Pasteur de Tunis) for his continuous interest in this study and for his support. Dr Benlasfar Zakaria and Ben Zakour Lotfi (laboratoire vétérinaire, Institut Pasteur de Tunis) are acknowledged for providing viper venom. This work was supported in part by a grant from the CMCU (Comité Mixte de Coopération Universitaire France-Tunisie), the ARC (Association pour la Recherche sur le Cancer), the GEFLUC (Groupement des Entreprises Françaises dans la Lutte contre le Cancer) and the Ligue Nationale contre le Cancer.
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Sarray, S., Berthet, V., Calvete, J. et al. Lebectin, a novel C-type lectin from Macrovipera lebetina venom, inhibits integrin-mediated adhesion, migration and invasion of human tumour cells. Lab Invest 84, 573–581 (2004). https://doi.org/10.1038/labinvest.3700088
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DOI: https://doi.org/10.1038/labinvest.3700088
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