Cell Electrofusion Visualized with Fluorescence Microscopy

I. Loading the cells with Cell trackers CMFDA and CMRA

1. Experiments were performed on previously prepared cells of mouse melanoma cell line (B16-F1). Cells are grown in two separated 25 cm² culture flasks (TPP, ZDA) to 70-80 % confluence in DMEM culture medium (Dulbecco’s modified Eagle’s medium) supplemented with 10 % fetal bovine serum, 0.15 mg/ml L-glutamine, 16 mg/ml gentamicin (all from Sigma-Aldrich, Germany), 200 units/ml crystacillin (Pliva, Croatia), and incubated in 5% CO₂ at 37°C.
2. Prepare two 10 mM stock solutions of Cell trackers (Invitrogen, USA) by adding 10.76 μl and 9 μl (for Green CMFDA and for Orange CMRA, respectively) of DMSO (Sigma-Aldrich, Germany) to 50 μg of the dye in the original Invitrogen vial. The stock solution can be stored in a refrigerator at 4°C for few months. Before starting the experiments, warm up the solution until the crystals of DMSO dissolve.
3. Prepare bicarbonate-free Krebs-Hepes buffer (130 mM NaCl, 4.7 mM KCl, 1.2 mM MgSO₄ , 1.2 mM KH₂PO₄, 11.7 mM D-glucose, 1.3 mM CaCl₂, 10 mM HEPES, pH 7.4). In two 15 ml Eppendorf tubes separately mix 2.1 μl of each stock solution (10 mM CMFDA or CMRA, respectively) in 3 ml of bicarbonate-free Krebs-Hepes buffer. This yields a “loading solution” containing approximately 7 μM CMFDA (or CMRA).
4. Rinse cells twice with bicarbonate-free Krebs-Hepes buffer and then insert loading solutions into the flasks. Incubate cells for 30 minutes in 5% CO₂ at 37 °C. During this first incubation reagents pass freely through cell membranes, but once inside the cell, the reagents are transformed into cell-impermeant fluorescent reaction products.
5. After first incubation, rinse and incubate cells with culture medium for another two hours in 5% CO₂ at 37°C.
6. Trypsinize cells in both flasks (loaded with CMFDA and CMRA) and mix red and green cells together in a ratio 1:1 in a 50 ml centrifuge tube (TPP, ZDA). Adjust cell concentration to 5 x 10⁶ cells/ml by dilution with DMEM medium or by concentration with centrifuge. Place a 20 μl drop of cell suspension in each well of 24 multiwell plate (TPP, ZDA). Incubate cells in 5 % CO₂ at 37 °C for 20 min to allow them to slightly attach to the surface of the well and establish cell contacts.

II. Electrofusion

1. Prepare isoosomolar potassium phosphate buffer (10 mM KH2PO4, 10 mM K₂HPO₄, 1mM MgCl₂, 250 mM sucrose) and hypoosmolar potassium phosphate buffer (10 mM KH2PO4, 10 mM K₂HPO₄, 1mM MgCl₂, 75 mM sucrose).
2. Place the multiwell with cells onto the microscope stage, position the electrodes at the bottom of the well and connect them to the pulse generator.
3. Wash the cells with 1 ml of isoosomolar potassium phosphate buffer. Add 350 μl of hypoosmolar potassium phosphate buffer in order to induce cell swelling. The buffer should cover the electrodes.
4. Leave cells in hypoosmolar buffer for 2 minutes before applying electric pulses. During this time influx of water molecules into the cells due to osmotic imbalance between the interior and the exterior of the cells cause an increase of cell volume. Electric pulses should be applied when cells are close to their maximum volumes, before regulatory volume decrease start.
5. To achieve optimal electrofusion and maintain cell viability, optimal parameters of electric pulses should be used. These depend on cell line used [1]. In this experiment a train of 8 rectangular pulses (each with duration of 100 μs at 1 Hz) is applied to each sample, using electroporation device (in our case Cliniporator, IGEA, Italy). The pulses are delivered to two parallel Pt/Ir wire electrodes with 0.8 mm diameter and 5 mm distance between them, creating an electric field of approximately 1200 V/cm between the electrodes in each well, except for the control well.
6. Leave the cells undisturbed for 10 minutes after pulse delivery. Determine the fusion yield by means of fluorescent and phase contrast microscopy.

III. Image acquisition and determination of the fusion yield

1. The cells are observed using a fluorescence microscope (in our case Zeiss AxioVert 200, Zeiss, Germany) equipped with an objective (x20) and a cooled CCD camera (VisiCam 1280, Visitron, Germany). The images are acquired in MetaMorph 7.1.1 (Molecular Devices, USA), but other similar acquisition software can also be used. CMFDA is excited with a monochromator (Polychrome IV, Visitron, Germany) at 492 nm and CMRA at 548 nm. The fluorescence of CMFDA and CMRA is acquired using two emission filters, one centered at 535 nm (HQ535/30m, for CMFDA) and the other centered at 510 nm (D605/55m, for CMRA, both Chroma, USA). The use of dichroic mirror (Q515LP) prevented the channel cross talk.
2. Acquire three images (phase contrast, red and green fluorescence) for five randomly chosen fields in each well. Create three channel images from each image triplet. In such image fluorescing cytoplasm can be seen together with the cell membranes. Fused cells can thus be easily determined [Figure 1].
3. Count all three types of cells (red, green and dually fluorescent) in each three channel image. Determine the percentage of dually fluorescent cells by dividing the number of dually fluorescent cells with the number of all cells in each image. Fusion yield is defined as the percentage of dually fluorescent cells multiplied by 2 since half of fused cells are not detected (when cells of the same color fuse).

Representative Results

Figure 1. Three channel microscopy image of B16F1 cells after electrofusion: phase contrast, CMRA fluorescence (excitation at 548 nm) and CMFDA fluorescence (excitation at 492 nm), objective magnification 20x