From: Research advances in the construction of stem cell-derived ovarian organoids
Tissue | Method | Species | Effect in vitro | Effect in vivo | Ref |
---|---|---|---|---|---|
Small tissue pieces | Rotated in 0.1% SDS at room temperature for 24Â h | Bovine and human | Supports ovarian somatic cell growth | Initiates puberty in ovariectomized mice | [56] |
1.5-mm-thick pieces | 1% Triton X-100 for 9 h and 0.5% SDS for 3 h at room temperature with agitation (100 rpm); treated with 200 U/mL DNase I in PBS at 37 °C for 12 h | Bama miniature pigs | Non-cytotoxic for rat ovarian cells, supported rat granulosa cell penetration and estradiol (E2) secretion | Minimal immunogenic response in rats | [57] |
Manageable strips | 1% sodium lauryl ester sulfate (SLES) for 48Â h, followed by DNase I in PBS for 24Â h | Women | Suitable cytocompatibility of the scaffolds | Oocyte growth, folliculogenesis, and endocrine function (estradiol and progesterone) in rats | [58] |
Tissue pieces | 0.1% sodium dodecyl sulfate (SDS) for 18–24 h, followed by 24 h of 1 mg/mL DNase treatment and washing | Women | Supports survival of human follicles and growth of murine follicles, with 39% reaching antral stages | Follicular recovery rates after three-weeks grafting were low but similar for both human (25%) and murine follicles (21%) | [59] |
Small pieces | 0.5% SDS for 3Â h, 1% Triton X-100 for 9Â h, and 2% deoxycholate for 12Â h | Gilts | Encouraged rapid cell adhesion and migration, with repopulating cells increasing in number and aggregating into cluster-like structures | - | [60] |
Whole organ | Immersed in 0.5% sodium dodecyl sulfate (SDS) in deionized water for 3 h and incubated overnight in 1% Triton X-100 in deionized water | Porcine | porcine ovarian cells(pOCs) recellularize the ECM-based scaffold and survive for 7 days, verifying ECM-based scaffolds’ ability to properly drive and address cell differentiation | - | [61] |
Pieces | Immersed and shaken in a combined solution of 2% sodium deoxycholate and 4% Triton X-100 for 36 h, with an exchange every 6 h. Followed by 36 h in 1% sodium dodecyl sulfate. Tissues were incubated in RNase/DNase solution (80 U/mL) for 6 h at 37 °C | Porcine | Scaffolds support GC survival for at least 15 days but might not sustain follicle growth for 7 days | Mainly caused an innate immune response in mice | [62] |
Small pieces | Treated in a 0.69% tris (hydroxymethyl) aminomethane and 2.5 mM sodium deoxycholate solution at 50Â rpm for 24Â h | Porcine | Preantral follicles cultured in a biomimetic ovary, and embryos were generated from MII oocytes | - | [63] |
Slices | Treated with 0.1% sodium dodecyl sulfate (SDS) in 1× phosphate-buffered saline (PBS) | Bovine | Supports follicle growth and survival | - | [52] |
Slices | Treated with 0.1% SDS and 0.02Â M NaOH for 12Â h | Bovine | No toxicity to human ovarian cells when cocultured for up to 72Â h | - | [64] |
Whole ovary | Submerged in liquid nitrogen for 10Â h, treated with 0.5% SDS for 2Â h, 1% Triton X-100 for 8Â h, and 2% deoxycholic acid for 8Â h. Rinsed with DI-H2O for 6Â h, changing every 2Â h to remove cell remnants | Porcine | Higher number of granulosa cells in vitro co-culture | - | [65] |