The CMV early enhancer/chicken β actin (CAG) promoter can be used to drive transgene expression during the differentiation of murine embryonic stem cells into vascular progenitors
© Alexopoulou et al; licensee BioMed Central Ltd. 2008
Received: 11 July 2007
Accepted: 11 January 2008
Published: 11 January 2008
Mouse embryonic stem cells cultured in vitro have the ability to differentiate into cells of the three germ layers as well as germ cells. The differentiation mimics early developmental events, including vasculogenesis and early angiogenesis and several differentiation systems are being used to identify factors that are important during the formation of the vascular system. Embryonic stem cells are difficult to transfect, while downregulation of promoter activity upon selection of stable transfectants has been reported, rendering the study of proteins by overexpression difficult.
CCE mouse embryonic stem cells were differentiated on collagen type IV for 4–5 days, Flk1+ mesodermal cells were sorted and replated either on collagen type IV in the presence of VEGFA to give rise to endothelial cells and smooth muscle cells or in collagen type I gels for the formation of vascular tubes. The activity of the CMV and β-actin promoters was downregulated during selection of stable transfectants and during differentiation to the Flk1 stage, while the CMV immediate enhancer/β-actin promoter in the pCAGIPuro-GFP vector led to 100% of stably transfected undifferentiated and differentiated cells expressing GFP. To further test this system we expressed syndecan-2 and -4 in these cells and demonstrated high levels of transgene expression in both undifferentiated cells and cells differentiated to the Flk1 stage.
Vectors containing the CAG promoter offer a valuable tool for the long term expression of transgenes during stem cell differentiation towards mesoderm, while the CMV and β-actin promoters lead to very poor transgene expression during this process.
Mouse embryonic stem (ES) cells are derived from the inner cell mass (ICM) of the mouse blastocyst and retain pluripotency when cultured in vitro in the presence of factors that inhibit differentiation, such as leukaemia inhibitory factor (LIF). However, when these factors are withdrawn, ES cells have the potential to differentiate into ectodermal, mesodermal, endodermal and germ cell lineages (reviewed in ). ES cells can differentiate either in suspension, forming embryoid bodies (EBs) or as two-dimensional adhesion cultures, either in the presence of feeder cells or extracellular matrix (ECM) molecules . The regulation of ES cell differentiation is currently under intense study, not least for potential therapeutic use. One important area of investigation is ES cell differentiation either in EBs or in 2-dimensional culture, along pathways recapitulating vasculogenesis and early angiogenesis [2, 3]. Related to this is delineation of functions for growth factors, adhesion molecules and transcription factors in the formation of the vasculature.
Elucidating the role of angiogenic factors during differentiation often requires over-expression of wild type and mutant proteins. Transfection of ES cells with plasmids using traditional electroporation and lipofectamine-based methods can be problematic [4–6]. Conflicting data about the activity of different promoters in undifferentiated ES cells have also been obtained, while several studies have suggested that transcriptional inactivation of promoters occurs during selection of stably transfected cells [7–9]. Another problem is obtaining stable transgene expression through stem cell differentiation. Several studies have looked at the efficacy of promoters in plasmid based vector systems with a view to obtaining high transient and stable expression in stem cells. For example, the CAG promoter has been used to express transgenes in undifferentiated ES cells as well as ES cells undergoing differentiation towards neuronal, myogenic and mesodermal cell types [10–12]. In the latter case a transfection system was used (ES cells expressing polyoma large T antigen and a vector with a polyoma virus origin of replication) leading to episomal propagation of the vector carrying the transgene of interest . Although episomal plasmid propagation may lead to very high levels of transgene expression due to a high copy number of plasmid per cell, certain experiments may require lower levels of overexpression that may be more physiologically relevant. Here, we compare the promoter activity of the CMV, chicken β-actin and CAG promoters in undifferentiated murine embryonic CCE cells as well as during differentiation to mesoderm. These cells are routinely used for differentiation into mesodermal lineages  and do not express the polyoma virus large T antigen allowing integration of transgenes into the host's genome. We demonstrate that of these vector systems, only plasmids containing the CAG promoter can be used for long term expression of genes during differentiation of two dimensional cultures of mouse embryonic CCE ES cells grown on collagen substrates towards mesoderm.
Results and Discussion
Differentiation of mesodermal cell lineages from mouse CCE ES cells
Flk1+ cells from either day 4 or day 5 cultures were FACS sorted and replated on collagen type IV-coated plates in the presence of VEGFA for a further 3 days (Fig. 1A). Double immunofluorescence microscopy for the EC markers VE-cadherin or Pecam-1 and the SMC marker α-smooth muscle actin (αSMA) (Fig. 1C, D) showed the presence of EC sheets surrounded by SMCs. Differentiation into ECs was VEGFA-dependent, as only αSMA+ cells were observed in its absence (data not shown). When Flk1+ cells were FACS sorted and plated in three dimensional collagen type I gels in the presence of VEGFA for an additional 6 days, the formation of angiogenic sprouts was observed (Fig. 1E, F). Tubular structures positive for the EC marker Pecam-1 were surrounded by αSMA+ SMCs/pericytes (Fig. 1G, H). The formation of tubes was dependent on VEGFA/Flk1 signalling, since no tubes formed in the absence of VEGFA or when Flk1- cells were sorted and cultured in the presence of VEGFA (data not shown). These data are in agreement with previous studies [13, 3] and suggest that this differentiation protocol mimics aspects of both vasculogenesis and early angiogenesis and is suitable for ectopic expression studies.
The CMV and β-actin promoters are not suitable for sustained expression of transgenes during CCE cell differentiation
Since a higher percentage of transiently transfected cells expressed GFP compared to the stably transfected cells (Fig. 2A–D), cells 2 days post transfection were used for differentiation to test whether this would lead to more GFP+ cells present at the Flk1 stage. However, the use of transiently transfected cells resulted in no cells expressing GFP on day 5 of differentiation (Fig. 2E, F). This suggested that stable integration of the transgene into the host's chromosome is required for its expression.
The above data suggest that to obtain sustained transgene expression in murine CCE cells and during differentiation into mesoderm, alternative promoters to the CMV and the chicken β-actin promoters are required. Furthermore, the above promoters driving expression in a vector that contains an IRES element were inactive in undifferentiated ES cells, in agreement with previous reports .
Vectors containing the CAG promoter can be used to express transgenes in murine CCE cells and during differentiation into mesoderm
Plasmids used in this study.
Antibiotic resistance to
GFP and Puromycin resistance
We then used the pCAGIPuro plasmid to express syndecans-2 and -4. Transfected cells were selected for puromycin resistance and the cells were differentiated on collagen type IV for 5 days. FACS analysis confirmed that high levels of cell surface expression of both proteins was achieved in undifferentiated as well as differentiated cells (Fig. 5D), although overexpression of these receptors had no effect on the percentage of Flk1+ cells obtained during differentiation (Fig. 5E).
Here we optimised a differentiation system of ES cells into Flk1+ mesodermal cells, ECs and SMCs and subsequently used the cells to form angiogenic sprouts in vitro. We then evaluated a number of plasmid vector systems for expressing transgenes during differentiation to Flk1+mesodermal cells and found that vectors which utilise the CAG promoter are most effective at driving gene expression and do not compromise the ability of stem cells to differentiate. The CAG promoter provides long term expression of transgenes in these cells however the system is most effective when the cells can be put under a selective pressure to express the transgene. For this reason bicistronic vectors containing an antibiotic resistance gene offers the best way of obtaining expression of transgenes during differentiation into mesodermal Flk1+ cells. This is in contrast to vectors containing the CMV and β-actin promoters which gave very low levels of expression. This presents a very useful tool for use in studies of angiogenesis and vasculogenesis.
Cell lines and culture conditions
CCE mES cells (StemCell Technologies) were grown in flasks coated with 0.1% gelatin (StemCell Technologies) in Dulbecco's Modified Eagle Medium (DMEM) (StemCell Technologies) supplemented with 15% foetal calf serum (FCS) (StemCell Technologies), 100 μM 2-mercaptoethanol (Invitrogen), 10 ng/ml LIF (StemCell Technologies), 2 mM glutamine (Invitrogen) and 100 μM MEM non-essential amino acids (StemCell Technologies). The CCE cells were maintained in a humidified incubator at 37°C and 5% CO2 in air. Rat embryo fibroblasts (REFs) were cultured in alpha-Minimum Essential Medium (αMEM; Cambrex) supplemented with 5% FCS (Cambrex).
The Flk1 (clone Avas12α; final concentration 50 μg/ml), the Pecam-1 (clone MEC13.3; 5 μg/ml) and the VE-cadherin (clone 11D4.1; 50 μg/ml) antibodies were from BD Pharmingen. The α smooth muscle actin (αSMA) antibody (1A4; 1 μg/ml) was from Sigma, the E-cadherin antibody (clone ECCD2; 20 μg/ml) was from Takara, Japan and the PDGFRβ antibody (10 μg/ml) was a kind gift from Dr W. Stallcup, Burnham Institute, La Jolla, California. R-Phycoerythrin-labelled SSEA-1 (clone 480; 4 μg/ml) and syndecan-2 antibodies (clone M140; 10 μg/ml) were from Santa Cruz. The polyclonal chicken anti-syndecan-4 antibody (Harlan Sera-Lab, UK) was raised against the N-terminal 20 amino acids of the mature human protein. Antibodies were affinity purified from plasma using standard procedures. The secondary antibodies (Molecular Probes) used were: Alexa-488 labelled donkey anti-rat IgG; Alexa-568 labelled goat anti-mouse IgG; Alexa-488 labelled goat anti-rabbit IgG; Alexa-488 labelled goat anti-chicken IgY, with working concentrations of 10 μg/ml.
Flow cytometry analysis and sorting (FACS)
Cells were detached with cell dissociation buffer (Invitrogen) and stained in FACS buffer (0.5% BSA, 2 mM EDTA in 1× PBS) at 4°C. For exclusion of dead cells, the nucleic acid dye Topro-3 (0.1 μM; Molecular Probes) was used. The cells were analysed by a four colour FACS Calibur (BD) and data for 10,000 live cells were analysed by the CellQuest software. Cells stained with secondary antibody only or empty vector transfected cells served as controls for background fluorescence. The gate M1 was set to include 1% of the control cells that exhibited the highest fluorescence within the population and cells were considered to be positive when contained within the gate M1. For FACS sorting, dead cells were excluded by propidium iodide staining (0.5 μg/ml; Molecular Probes). Cell populations were sorted by FACS Diva (BD) and collected in sterile tubes in 2 ml medium. Flk1+ cells were plated either on collagen type IV-coated plates or in collagen type I gels.
Cells on glass coverslips were fixed in acetone (-20°C) for 2 min. After washing in PBS, cultures were incubated with the appropriate concentration of primary antibody in PBS for 1 h at 37°C. Secondary antibody incubation for 1 h at 37°C was followed by further washing in PBS and coverslips were mounted with Immuno-Fluor (MP Biomedicals). Controls included staining with secondary antibody only, while in double labelling experiments, controls included incubation with one primary antibody and both secondary antibodies. Inappropriate cross-reactivity was minimal. Samples were examined on an Olympus Provis AX module fluorescence microscope (objective: UPlanApo 40× 1.0 oil). The images were collected using a SPOT Insight Mono digital camera and were processed by Adobe Photoshop 7.0.
ES cell differentiation into mesodermal, endothelial and smooth muscle cells
Differentiation of CCE cells first into Flk1+ mesodermal cells and then into VE-cadherin+ ECs and αSMA+ SMCs that were able to form angiogenic sprouts was achieved following the protocol described in . Micrographs were taken on an Olympus DP50 microscope and digital camera system. Images were processed using the Viewfinder Lite software and Adobe Photoshop 7.0.
Three dimensional collagen type I cultures were fixed with 3.5% paraformaldehyde for 1 h at room temperature. The samples were washed 3 × 15 min with PBS and were released from the wells and embedded in an 8% gelatin solution to provide rigidity. Fixation with paraformaldehyde was repeated for 1 h at room temperature. Excess gelatin was removed and samples were stored in 0.02% Sodium Azide in 1× PBS at 4°C. Sections of 200 μm thickness were prepared on a Micro-Cut H1200 vibrotome (Bio-Rad). Sections were permeabilised with 0.1% Triton X-100 for 1 h at room temperature, then washed 3 × 15 min with PBS. Primary antibodies against Pecam-1 and αSMA were added at appropriate concentrations and incubated overnight at 4°C. Sections were washed with PBS, then incubated in secondary antibody for 5 h at room temperature. After further extensive washing, sections were mounted onto slides using Gene Frame gaskets (Advanced Biotechnologies) and were sealed with coverslips. The samples were examined on a Leica DM-IRBE confocal microscope and images were processed using Leica TCS-NT and Adobe Photoshop 7.0 software.
RNA extraction and RT-PCR
Primers used in this study.
Deletion of CMV promoter from pIRES2-EGFP
Deletion of CMV promoter from pIRES2-EGFP
Vectors and Cloning
The pEGFP-N1 plasmid was from Clontech. The pMC1neo PolyA plasmid was from Stratagene. The pCAGGS plasmid was a kind gift from Dr C. Huxley , Imperial College London. The pCAGIPuro vector was a kind gift from Dr H. Niwa, Riken Centre for Developmental Biology, Japan (Table 1).
Full length syndecan-2 and -4 cDNA obtained from RT-PCR of mouse brain was cloned into the EcoRI site of vector pCAGIPuro to create pCAGIPuro-sdc2 and pCAGIPuro-sdc4, respectively using the primers described in Table 2.
The GFP cDNA from pCAGGS was removed by EcoRI digestion, the product was gel purified then ligated to the EcoRI site of pCAGIPuro to create pCAGIPuro-GFP.
To insert the neomycin resistance cassette into the pCAGGS vector, pMC1neo polyA was digested with SalI and XhoI to release the neomycin resistance cassette, which was then ligated into the SalI site of pCAGGS to create pCAGGSneo-GFP.
For control purposes, the GFP cDNA was removed from pCAGGS by restriction digest with the enzyme EcoRI to create pCAGGS-ev. The neomycin resistance cassette from pMC1neo PolyA was then ligated to the SalI site of pCAGGS-ev to create pCAGGSneo-EV.
To create pIRES2-EGFP(β-actin), the EcoRI/SalI fragment of pLK444  containing the β-actin promoter was gel purified and the overhangs were filled using Pfu polymerase. To remove the CMV promoter from pIRES2-EGFP (Clontech), PCR was performed using the primer pair IRESdelfor and IRESdelrev (Table 2). The primers were designed to yield a plasmid backbone of the pIRES2-EGFP containing an EcoRV site in place of the CMV promoter (pIRES2-EGFP-CMV). pIRES-EGFP-CMV was then cut with EcoRV, dephosphorylated and ligated to the blunt-ended β-actin fragment to generate pIRES2-EGFP(β-actin).
To create pLK444-GFP, the EGFP cDNA was amplified by PCR from pEGFP-N1 using the primer pair GFPfor and GFPrev (Table 2). The PCR product was digested with HindIII and BamHI and ligated to the HindIII/BamHI sites of pLK444 to yield pLK444-GFP.
For transfection in suspension, 150,000 CCE cells were plated per well of a six-well plate 24 h prior to transfection. Cells were trypsinised and washed in serum free DMEM. 1 μg DNA, 10 μl lipofectamine (Invitrogen) and serum free DMEM to a final volume of 50 μl were added to the cell pellet and incubated for 10 min at room temperature before transfer to a well of a 6-well plate containing 3 ml culture medium (supplemented with FCS). Fresh medium was added after 24 h. Fibroblasts were transfected with lipofectamine following standard procedures.
bovine serum albumin
fluorescence-activated cell sorting
green fluorescent protein
internal ribosomal entry site
leukemia inhibitory factor
phosphate buffered saline
platelet derived growth factor receptor
stage specific embryonic antigen
vascular endothelial growth factor.
This work was supported by the Wellcome Trust Program Grant 065940 to JRC and Wellcome Trust Studentship 069369 to ANA. We gratefully acknowledge the generous gift of the pCAGIPuro vector from Dr. Hitoshi Niwa of the RIKEN Centre for Developmental Biology, Kobe, Japan. In addition we would like to thank Dr. Clare Huxley of Imperial College for her hep and advice.
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