Method for in vitro culture of ovarian follicles
一种体外培养、卵泡的技术,应用在培养过程、组织培养、细胞培养活性剂等方向,能够解决不可能评价等问题
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Embodiment 1
[0040] Isolation and preculture of secondary follicles ( figure 1 Step 1) in:
[0041] Ovarian tissue was isolated from 12- to 14-day-old F1 generation C57B1 / j6XCBAca hybrid mice and placed in GlutaMAXI TM Petri dishes of Leibovitz's L15 medium (Gibco BRL 31415-029) containing 10% HIA FBS (heat-inactivated fetal bovine serum) and 0.1% penicillin-streptomycin mixture (Gibco BRL 3032908). The ovaries remove the fallopian tubes and fat.
[0042] The surface of the ovary is scratched with a needle and the follicles are released in suspension in L15 medium. Under normal conditions, 30 to 40 suitable follicles can be obtained from each ovary by this isolation method.
[0043] To isolate primary follicles, use 7- to 8-day-old mice. In this case 10 to 15 suitable follicles can be obtained from each ovary.
Embodiment 2
[0045] The method of the present invention selects follicles ( figure 1 Step 2) in:
Embodiment 3
[0049] The establishment and application of follicular storage ( figure 1 Step 3) in:
[0050] Follicles can be stored using cryopreservation techniques known to those skilled in the art. The next paragraph describes an embodiment of this technique.
[0051] The follicles obtained in Example 2 were collected into plastic cryovials (Simport, Quebec, Canada). Twenty-five follicles per vial were suspended in 150 microliters of L15 medium supplemented with 10% heat-inactivated FCS and 1.5M DMSO. Slow freezing was performed using a programmable freezer (Cell Freezer R204, Planer, Sunbury-on-Thames, UK) that could be controlled. Follicles were equilibrated in the 4°C freezing mixture for 15 min and then cooled to -7°C at a rate of 2°C / min. After manual inoculation, the temperature was lowered to -40°C at a rate of -0.3°C / min. Follicles were rapidly cooled to -110°C at a rate of -50°C / min before storage in liquid nitrogen.
[0052] Follicles were ultra-rapidly thawed by heating...
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