Table 3.
Species | Age | Initial follicle stage and isolation method | Culture system and interval | Basal media, supplement and O2 level | Oocyte assessment and outcomes | References |
---|---|---|---|---|---|---|
Olive baboon | 9–16 years | Multilayer preantral; Liberase and DNase |
Fibrin-0.25% (w/v) alginate-matrigel embedded individual culture for 14 days followed by 48-h IVM | αMEM, 5 μg/ml insulin; No rhFSH; No O2 control |
2/16 MIIs with typical spindle structure by immunofluorescence | [56] |
Rhesus macaque | 6.4 years in average | Small antral; Mechanical |
Individual culture without or with 0.25% (w/v) alginate-embedding for 34 h | αMEM, 5 μg/ml insulin; 220 mIU/ml rhFSH, without or with 200 IU/ml hCG; No O2 control |
-Alginate/-hCG: 4/27 MIIs, −alginate/+hCG: 14/41 MIIs, and + alginate/+hCG: 4/11 MIIs by light microscopy | [57] |
4–9 years | Multilayer preantral; Mechanical |
Individual culture in media droplets covered with oil for 14 days followed by IVM | αMEM, 5 μg/ml insulin; 200 mIU/ml rhFSH, 100 or 200 mIU/ml rhLH; No O2 control |
2/24 MIIs by light microscopy | [58] | |
5–10 years | Secondary; Collagenase and DNase |
0.25% (w/v) alginate embedded individual culture for 40 days followed by 34-h 100 ng/ml hCG treatment | αMEM, 5 μg/ml insulin; 0.3 (low) or 15 (high) ng/ml rhFSH; No O2 control or 5% O2 |
High rhFSH/5% O2: 1/25 MII with typical spindle structure by immunofluorescence; Low rhFSH/5% O2: 1/8 MII developed to a 2-cell embryo after ICSI; Low rhFSH/no O2 control: 1 MII by light microscopy |
[59] | |
7–14 years | Secondary and primary; Mechanical |
Secondary: 0.25% (w/v) alginate embedded individual culture for 5 weeks, and primary: fibrin-0.25% (w/v) alginate embedded individual culture for 13 weeks followed by 34-h 100 ng/ml hCG treatment | αMEM, 5 μg/ml insulin; 3 ng/ml rhFSH; 5% O2 |
Secondary: 1/15 MII developed to the morula stage after ICSI; Primary: 1/5 MII formed a zygote after ICSI |
[60] | |
7 years | Secondary; Mechanical |
0.25% (w/v) alginate embedded individual culture for 5 weeks followed by 34-h 100 ng/ml hCG treatment | αMEM, 5 μg/ml insulin; 3 ng/ml rhFSH in week 0–3 followed by 0.3 ng/ml in week 4–5; 5% O2 |
2/22 MIIs developed to the morula stage after IVF | [61] | |
Reproductive age | Secondary; Mechanical |
0.25% (w/v) alginate embedded individual culture for 40 days followed by 34-h 100 ng/ml hCG treatment | αMEM, 5 μg/ml insulin; 3 ng/ml rhFSH in Days 0–20 followed by 0.3 ng/ml in Days 21–40, without or without androgen modulation; 5% O2 |
-Androgen modulation: 4/49 MIIs with 2 formed zygotes and 1 developed to the morula stage after IVF; TRL steroid depletion+50 ng/ml T: 1/13 MII, and TRL steroid depletion+50 ng/ml DHT: 1/13 MII formed a zygote after IVF |
[62] | |
9.5 ± 2.1 years | Secondary; Mechanical |
0.25% (w/v) alginate embedded individual culture for 5 weeks followed by 34-h 100 ng/ml hCG treatment | αMEM, 0.5 μg/ml insulin; 3 ng/ml/100 mIU rhFSH in week 0–3 followed by 0.3 ng/ml in week 4–5, without or without estrogen modulation; 5% O2 |
-Estrogen modulation: 1/13 MII, and TRL steroid depletion+100 ng/ml E2: 1/14 MII developed to the morula stage after IVF | [63] | |
6–14 years | Secondary; Mechanical |
0.15% (w/v) alginate embedded individual culture for 5 weeks followed by 34-h 100 ng/ml hCG treatment | αMEM, 5 μg/ml insulin; 1 ng/ml rhFSH, 25 pg/ml VD3 in weeks 3–5; 5% O2 |
1/22 MII by light microscopy | [64] | |
7–13 years | Secondary; Mechanical |
Individual culture in 96-well round-bottom ultra-low attachment plate for 5 weeks followed by 34-h 100 ng/ml hCG treatment | αMEM, 5 μg/ml insulin; 1 ng/ml rhFSH, without or with 100 ng/ml rhAMH in week 0–2; No O2 control |
-rhAMH: 1/14 MII, and + rhAMH: 2/19 MIIs developed to the morula stage after IVF | [65] | |
Reproductive age | Secondary; Mechanical |
0.25% (w/v) alginate embedded individual culture for 40 days followed by 34-h 100 ng/ml hCG treatment | αMEM, 5 μg/ml insulin; 1 ng/ml rhFSH, 120 ng/ml AMH-Ab in week 3–5; 5% O2 |
1/10 MII developed to an 8-cell embryo after IVF | [68] | |
6–10 years | Secondary and primary; Mechanical |
Secondary: individual culture in 96-well round-bottom ultra-low attachment plate for 5 weeks, and primary: group culture in 96-well round-bottom ultra-low attachment plate for 7 weeks followed by 34-h 100 ng/ml hCG treatment | αMEM, 5 μg/ml insulin; 1 ng/ml rhFSH, primary: 100 ng/ml rhAMH in week 0–5 and secondary: without or with AMH modulation; No O2 control |
Secondary/-rhAMH modulation: 2/16 MIIs developed to the morula stage after ICSI; Secondary/+rhAMH in week 0–3 + AMH-Ab in week 4–5: 10/36 MIIs with 9 developed to the morula stage and 1 developed to the blastocyst stage after ICSI; Primary: 2/34 MII developed to the morula stage after IVF |
[66] |
AMH, anti-Müllerian hormone; AMH-Ab, neutralizing anti-human anti-Müllerian hormone antibody; DHT, dihydrotestosterone; DNase, deoxyribonuclease; E2, estradiol; hCG, human chorionic gonadotropin; ICSI, intracytoplasmic sperm injection; IVF, in vitro fertilization; IVM, in vitro maturation; αMEM, alpha minimum essential medium; MII, metaphase II; O2, oxygen; rhAMH, anti-Müllerian hormone; rhFSH, human recombinant follicle-stimulating hormone; rhLH, human recombinant luteinizing hormone; T, testosterone; TRL, trilostane; VD3, 1α,25-dihydroxyvitamin D3.