Development of a one-step embryonic stem cell-based assay for the screening of sprouting angiogenesis
- Bastien Hermant†1, 2, 3,
- Agnès Desroches-Castan†1, 2, 3, 4,
- Marie-Laure Dubessay1, 2, 3,
- Marie-Hélène Prandini1, 2, 3,
- Philippe Huber1, 2, 3 and
- Daniel Vittet1, 2, 3Email author
© Hermant et al; licensee BioMed Central Ltd. 2007
Received: 24 January 2007
Accepted: 16 April 2007
Published: 16 April 2007
Angiogenesis assays are important tools for the identification of regulatory molecules and the potential development of therapeutic strategies to modulate neovascularization. Although numerous in vitro angiogenesis models have been developed in the past, they exhibit limitations since they do not recapitulate the entire angiogenic process or correspond to multi-step procedures that are not easy to use. Convenient, reliable, easily quantifiable and physiologically relevant assays are still needed for pharmacological screenings of angiogenesis.
Here, we have optimized an angiogenesis model based on ES cell differentiation for screening experiments. We have established conditions leading to angiogenic sprouting of embryoid bodies during ES cell differentiation in type I three-dimensional collagen gels. Immunostaining experiments carried out during these cultures showed the formation of numerous buds comprising CD31 positive cells, after 11 days of culture of ES cells. Moreover, this one-step model has been validated in response to activators and inhibitors of angiogenesis. Sprouting was specifically stimulated in the presence of VEGF and FGF2. Alternatively, endothelial sprouting induced by angiogenic activators was inhibited by angiogenesis inhibitors such as angiostatin, TGFβ and PF4. Sprouting angiogenesis can be easily quantified by image analysis after immunostaining of endothelial cells with CD31 pan-endothelial marker.
Taken together, these data clearly validate that this one-step ES differentiation model constitutes a simple and versatile angiogenesis system that should facilitate, in future investigations, the screening of both activators and inhibitors of angiogenesis.
Angiogenesis, the process of growth of blood capillaries from the pre-existing vascular tree, is a complex phenomenon that is either associated with or involved in the development of numerous physiological or pathological situations [1, 2]. Among them, angiogenesis is considered crucial for revascularization after cardiac ischemia, and is also implicated in the pathogenesis of rheumatoid arthritis, diabetic retinopathy, and tumoral progression. In particular, numerous clinical and experimental data show that the growth of cancerous tumors and the formation of metastases are highly dependent on the establishment of tumoral neovascularization from the pre-existing vascular network . The tumor microvascular network then represents a new target for cancer treatment and the identification and characterization of molecules that control the formation of blood vessels become of interest in the development of anti-cancer therapies. In addition, there is also a great interest in combining antiangiogenic therapy with other conventional cytotoxic therapies in cancer treatment since several studies have demonstrated that the delivery of therapeutics may be increased during vessel normalization induced by angiostatics .
Several angiogenesis regulators have now been identified and characterized . Although first clinical trials of single agent antiangiogenic treatment have not always given satisfactory results, the use of an antiangiogenic therapy still remains highly promising in pathologies where angiogenesis is undesired . In contrast, strategies aimed at stimulating angiogenesis could also present interest in many cases where neovascularization is needed such as after cardiac ischemia or after tissue graft. Then, there is a great challenge to find new potential angiogenesis activators or inhibitors that may be candidate for therapeutics. Within this context, the setting up of models for screening active molecules (angioactive or angiostatic) on the angiogenic response, is of considerable importance. Numerous in vitro angiogenesis models have been developed [6, 7]. They are either two-dimensional (2D) models such as conventional cell proliferation and migration tests or more elaborated three-dimensional (3D) assays. Concerning 3D angiogenesis models, assays involving Matrigel, a matrix derived from mouse Engelbreth-Holm-Swarm sarcoma, are among the most common commercially available in vitro angiogenesis assays. Other 3D models are based on the use of fibrin or type-1 collagen as a support matrix for endothelial cells. However, both 2D and 3D models mostly involve the study of one particular step of the angiogenic response, but do not recapitulate the entire angiogenic process including proliferation, migration and tubulogenesis. Although they exhibit some interest for primary screening because of their simplicity, an assay recapitulating all the sprouting angiogenic process should be preferable since it would be more physiologically relevant. Other models that more closely recapitulate the sprouting angiogenic response have therefore been established. They include models based on the 3D culture of endothelial cell-coated microcarriers or endothelial cell spheroids embedded in collagen gels [8, 9]. However, they require multi-step procedures and are not easy to perform. Mouse embryonic stem cells (ES cells) have also been shown to be a good alternative as a system for the study of differentiation towards the endothelial lineage [10–14]. In addition, this cellular system, into which genetic modifications can easily be introduced, can go through most of the stages of budding angiogenesis as observed in vivo [15–17]. In the previously described ES cell model, two steps are required for angiogenesis to proceed . First, ES cells are induced to differentiate into embryoid bodies (EBs). EBs are then collected and further cultured into a type I 3D collagen matrix for another period, during which the EB primary vascular structures extend and invade the collagen matrix, leading to complex and ramified endothelial sprouts mimicking the sprouting angiogenesis process. This two-step model makes possible to carry out qualitative and quantitative studies by cell imaging . All of these characteristics together, therefore, make it a powerful study model that enables to evaluate, in vitro, the efficiency of active molecules with respect to both vascular development and angiogenesis, and to improve the understanding of the molecular mechanisms that are called into play during these responses.
Ideally, an in vitro angiogenesis assay suitable for the screening of potentially active compounds should be convenient, reliable, easily quantifiable and physiologically relevant. In addition, it should allow evaluation of multiple samples in one experiment. Although the ES cell-based angiogenesis model fills most of these requirements, it remains time consuming since it proceeds in two culture steps and requires many manual interventions before being processed for angiogenesis visualization and quantification that may constitute an inconvenient for screening experiments.
Matrix proteins, including type I collagen, support cell differentiation in many lineages . A recent study indicated that ES cells can undergo multi-lineage differentiation including differentiation into cells of the endothelial lineage when plated directly into collagen gels . A 3D collagen environment for ES cell differentiation then appears to constitute a mean to improve ES two-step angiogenesis models. Moreover, some early unpublished data have also postulated that ES cell differentiation into a mixture of type I and type III collagens could be used for the screening of angiogenesis regulating factors . In this context, the aim of the present work was to simplify the in vitro differentiation model of ES cells in order to establish and to validate a one-step model that may be relevant for the preclinical screening of active molecules on angiogenesis.
In this paper, we report the development and the validation of a simple one-step ES cell differentiation model for the screening of angiogenesis regulators. We provide evidence that this one-step model can recapitulate the various stages of sprouting angiogenesis, as initially reported for previously established two-step ES differentiation models. Moreover, we describe a standardized procedure to obtain reproducible and efficient development of endothelial sprouts from EBs using this one-step model. Compared with the two-step procedure, only one growth factor addition is required after initial seeding without any further intervention, which greatly simplifies the test. In comparison with other available in vitro models, the one-step ES cell based angiogenesis model shows the major advantage of reproducing at least three aspects of the sprouting angiogenesis response: proliferation, migration and vascular morphogenesis. As previously observed in two-step ES cell differentiation procedures [22, 15, 21], the vascular endothelial sprouts that develop in the one-step ES cell model are associated with pericytes, which confers to the one-step model superiority to many in vitro angiogenesis models that mostly recapitulate only limited aspects of the angiogenic response .
Multiple steps of the angiogenic process may be altered by an angiogenesis-targeted drug. The fact that the ES differentiation model mimicks the complexity of the sprouting angiogenesis response makes it relevant for further identification of novel molecules and mechanisms regulating this process. EB endothelial sprouting was specifically induced by angioactive molecules, namely VEGF and to a minor extent FGF2, and inhibited by known angiostatic factors. These data validate the one-step ES differentiation model as a versatile angiogenesis system for the screening of both activators and inhibitors of angiogenesis.
The ES differentiation one-step procedure is easier to use than the other 3D angiogenesis existing models since they all proceed into two steps and require extensive manipulations. Screening experiments can be performed in both 6-well or 12-well-microplaque format that could be very useful for further adaptation of the model for automatization and may be convenient to further characterize molecules identified by primary screens using less complete cellular models.
Thus, the one-step ES-based angiogenesis model, that allows routine and reproducible accomplishment in a reduced time, constitutes a good alternative for existing in vitro angiogenesis models. In addition, in view of its simplicity, it allows an easy transfer to non-specialist investigators. We expect the one-step ES angiogenesis model to be particularly valuable to extend drug discovery screening.
Embryonic Stem (ES) cell differentiation
CJ7-ES cells , and on rare occasions R1-ES cells , were used. ES cells were cultured on gelatin-coated cell culture dishes and were maintained undifferentiated in the presence of 103 U/ml Leukemia Inhibitory Factor (LIF) (ESGRO, Chemicon, Temecula, CA) as previously described . At day 0, to initiate the differentiation, cells were collected by trypsin, counted and resuspended in Iscove modified Dulbecco's medium (IMDM), before being gently mixed into a type I collagen-medium in the presence of angiogenic factors: 50 ng/ml VEGF (Peprotech, Rocky Hill, NJ) and 100 ng/ml FGF2(a generous gift from Dr Ana Maria Gonzales, Queen Elizabeth medical center, Birmingham, UK). Final composition of the collagen-medium was 15% fetal calf serum (FCS) (Biowest, Nuaillé, France), 450 μM of monothioglycerol, 1.2 mg/ml type I collagen (BD Biosciences, Bedford, MA) neutralized with 1 N NaOH (according to the manufacturer recommendation), 10 μg/ml insulin and 0.5% penicillin-streptomycin. Practically, final ES cell suspensions in the collagen medium were obtained by mixing ES cells in collagen solution with a concentrated solution of medium as previously detailed in the procedure for EB secondary culture into type I collagen gels . ES cells in collagen-medium were poured either in 35-mm bacterial dishes (1.5 ml per well) or in 12-well bacterial microplaque (1 ml per well) at a concentration of 2,000 cells/well, leading to the obtention of a 1.5 mm-thick or a 2.4 mm-thick gel, respectively. The cells were incubated at 37°C, in a 5% CO2, 95% air atmosphere. At day 6, a second addition of VEGF and FGF2 was done using the same concentrations of growth factors as used at day 0. Factors were diluted either into 100 μl or into 200 μl medium lacking collagen before being added to 12-well plates or 35-mm dishes, respectively. Cultures were stopped at day 11 for EBs analysis.
At day 11 of differentiation, collagen gels containing EBs were collected on glass slides. Dehydration was obtained using nylon linen and adsorbent cards, thus allowing 2D projection of the sprouts. EBs were then fixed using 3% paraformaldehyde in PBS for 15 minutes at room temperature. After three washes with PBS, slides were incubated 1 hour at room temperature with rat anti-mouse CD31 monoclonal antibody MEC-13.3 , (a generous gift from Dr A. Vecchi, Mario Negri Institute, Milan, Italy), used as undiluted hybridoma supernatant. After 3 rinses, slides were incubated for one hour at room temperature with cyanine 3-conjugated goat anti-rat IgG (Jackson Immunoresearch Laboratories, West Grove, PA) diluted 1:300. After three further washes in PBS, slides were counterstained with Hoescht 33258. Slides were mounted in Fluorsave (Calbiochem, La Jolla, CA).
In some experiments, EBs were double labeled with rat anti-mouse CD31 monoclonal antibody MEC13.3, used as undiluted hybridoma supernatant, and rabbit antibodies directed against rat proteoglycan NG2 (1 μg/ml) (a generous gift from Dr W.B. Stallcup, La Jolla, CA) or against human von Willebrand factor (vWF) (DakoCytomation, Trappes, France) (dilution 1:500), and the staining was revealed by incubation with a mixture of cyanine 3-conjugated goat anti-rabbit IgG (Jackson Immunoresearch Laboratories) and of Alexa488-conjugated goat anti-rat IgG (Molecular Probes, Eugene, OR). When immunofluorescence experiments were performed with vWF antibodies, EBs were fixed and permeabilized with 3% paraformaldehyde and 0.5% Triton X-100 for 3 min, followed by a supplementary 15 min fixation with 3% paraformaldehyde alone, before rinses with PBS and immunostainings.
When tested, angiogenesis inhibitors were added at day 6 at the same time of the second angiogenesis activators addition. They were used at optimal concentrations known to affect endothelial sprouting from EBs in the two-step ES cell angiogenesis model [15, 33]. Platelet factor 4 (PF4) (Diagnostica Stago, Asnières, france) was used at 2.5 μg/ml; angiostatin (fragment K1–4) (Calbiochem) was used at 2.5 μg/ml and Transforming Growth factor β1 (TGFβ) (R&D Systems, Abingdon, UK) was used at 10 ng/ml. Inhibitors were added with angiogenesis growth factor activators (VEGF and FGF2) diluted in differentiation medium to each well (100 μl) or dishes (200 μl).
After dehydration of the collagen gels to allow the complete 2D projection of the sprouts and immunostaining with anti-CD31 antibodies, the slides were observed using a Zeiss Axioplan fluorescence microscope (Zeiss, Oberkochen, Germany). Images were captured, at 5× or at 10× magnification, depending on the size of the sprouting EBs, with a computer-supported digital Spot RT camera using Spot advanced software (Diagnostic instruments, Sterling Heights, MI). In order to quantify the sprouting, images were processed for morphometric analysis using Metamorph Offline software (Molecular Devices, Downingtown, PA). A macrocommand was edited to give the total endothelial sprout length of each EB after binarization and skeletonization of the image of the CD31 staining.
The authors are indebted to Dr Rolande Berthier and Mrs Annie Schweitzer, who first initiated the ES cell differentiation procedure in collagen gels in the laboratory, for having shared with them protocols and expertise. The authors are also grateful to Dr Ana Maria Gonzales (Queen Elizabeth medical center, Birmingham, UK) for the generous gift of recombinant FGF2, to Dr Thomas Gridley (The Jackson Laboratory, Bar harbor, ME) and to Dr Dietmar Vestweber (University of Munster, Munster, Germany) for the CJ7 ES cell line, to Dr Andras Nagy (Samuel Lunenfeld Research Institute, Toronto, Canada) for the R1 ES cell line, to Dr William B. Stallcup (The Burnham Institute, La Jolla, CA) for rabbit antibodies against recombinant rat NG2, and to Dr Annunciata Vecchi (Mario Negri institute, Milan, Italy) for providing the MEC13 hybridoma. The authors would like to thank Dr Jean-Baptiste Sibarita (Institut Curie, Paris, France) and Dr Marie-George Côme (Roper Scientific, Evry, France) for macrocommand edition on MetaMorph software for image analysis and endothelial sprouting quantitation.
This study was supported by Inserm, CEA, The Ligue Nationale Française Contre le Cancer (Bastien Hermant was a fellow from Ligue Nationale Française Contre le Cancer), The Région Rhône-Alpes, The Canceropôle Lyon Auvergne Rhône-Alpes and the Groupement d'Entreprises Françaises de Lutte contre le Cancer (GEFLUC) Dauphiné-savoie.
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