Table 2:
Model | In vitro effects | Pregnancy outcome | Ref |
---|---|---|---|
RWV versus static controls, alginate encapsulated isolated cultured secondary follicles or ovarian fragments | Decreased proliferation of granulosa cells and oocyte GDF9 in fragments; growth of secondary follicle oocytes in alginate, but abnormal oocyte ultrastructure | ND | 41 |
RCCS with high aspect ratio culture vessels versus static controls, mouse GV oocytes matured in vitro | Inhibited oocyte maturation, abnormal meiotic spindles with abnormal tubulin localization in both meiosis I and II | ND | 55 |
Mouse oocytes and sperm IVF and cultured to blastocyst stage in 3D clinostat versus static 1g controls | Minimal effect fertilization rate NS development to 2-cell stage at 24h; ↓development to blastocyst at 96h |
↓Birth rate of implanted 2-cell embryos and blastocysts | 57 |
RCCS with high aspect ratio culture vessels and rotation and static culture control groups; 2-cell (1.5 dpc), 8-cell (2.5 dpc), and morula or early blastocyst (3.5 dpc) embryos harvested from mice and cultured for 24 h in simulated microgravity, then for 48 h in static culture. Static culture control group | 2-cell and 8-cell arrested development at 24h and 70% and 100% death by 72h, respectively; 40% of 3.5 dpc embryos progressed to late blastocyst stage; ↑SAPK phosphorylation after 24h culture of 3.5 dpc embryos; rotational controls had similar but less severe effects |
ND | 58 |
High aspect ratio vessel RCCS with spinner flask rotational controls or clinostat with static controls; Cultured luteal cells from corpora lutea of pregnant rats |
↓progesterone secretion both microgravity groups; ↑increased DNA damage, apoptosis, ↓active mitochondria in clinostat group |
ND | 42,43 |
Abbreviations: dpc: days post coitum; GV: germinal vesicle stage prior to completion of first meiotic division; IVF: in vitro fertilization; ND: not determined; NS: not statistically significant; RWV: rotating wall vessel; RCCS: rotary cell culture system