All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.
1. Isolation of porcine cumulus-oocyte complexes
- To collect material for the isolation of ovarian follicles, excise porcine ovaries from prepubertal gilts (approximately 6-7 months of age, weighing 70 to 80 kg) at a local slaughterhouse. Choose approximately 20 pig ovaries from 10 animals for cumulus-oocyte complexes (COCs) isolation in each experiment.
NOTE: Assuming each ovary yields 3–5 follicles, the total number of follicles varies from 60 to 100.
- Place ovaries in a thermos with sterile phosphate-buffered saline (PBS; pH 7.4; 38 °C) containing 1% antimycotic solution (AAS). Ensure that the experimental material is transported to the laboratory within 1 h where it is rinsed twice with sterile PBS containing antibiotics.
- After rinsing the ovaries, transfer them to the beaker filled with handling medium (HM) (Table of Materials) and store them in an incubator at 38 °C for the time of all manipulations.
NOTE: For optimal results during oocyte handling, carry out all procedures in DMEM/F12 medium (handling medium, HM) with the addition of 2.5% antibiotic/AAS and 10% fetal bovine serum (FBS) and control the pH at the CO2 level in the environment, on a heating table with temperature control (38 °C) and under the laminar flow hood to minimize bacterial contamination.
- From large porcine follicles (6-8 mm in diameter) collect follicular fluid (FF) by aspiration and centrifugation at 100 x g for 10 min at room temperature. After that, filter the supernatant using a sterile syringe attached to 0.2 μm membrane pore filters and snap freeze at -80 ° C.
NOTE: Use an insulin syringe (u- 40) for aspiration of follicular fluid.
- Ensure that only healthy, medium-sized follicles (4-6 mm in diameter) are selected for COCs isolation.
NOTE: COCs of grade I, possessing an intact and round oocyte with homogeneous ooplasm and multi-layered (at least 3-4) compact cumulus are considered suitable for further 3D IVM procedure.
- To isolate COCs, transfer 2-3 ovaries to a sterile 10 cm diameter Petri dish filled with HM. Isolate COCs from medium-sized follicles by following one of the procedures below.
- Gently cut the surface of the protruding ovarian follicles with a sterile surgical blade 15C. This will cause the follicular fluid along with COCs to flow out into the Petri dish.
- Aspirate the follicular content using 28 G needle having a size of 5/8” attached to a disposable syringe and transfer it into the Petri dish.
NOTE: Discard the remains of ovarian tissue. Subsequent stages of isolation are carried out under a stereomicroscope.
- Prepare 3–5 60 mm IVF Petri dishes.
- Add 1 mL of HM to the central wells and place 3-4 drops of HM (50 μL per drop) in their outer rings.
- Then, using a polycarbonate micropipette, move the undamaged COCs to drops of HM in the outer rings to rinse them briefly for 3-4 times.
- At the end, individually transfer them into the central well. Store these IVF plates in an incubator for further procedures.