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Updated: May 31, 2026

In Vitro Growth of Mouse Preantral Follicles Under Simulated Microgravity
Published on: December 17, 2017
Simulated microgravity compromises mouse oocyte maturation by disrupting meiotic spindle organization and inducing
Changli Wu1, Xinzheng Guo, Fang Wang
1Guangdong Provincial Key Lab of Agro-Animal Genomics and Molecular Breeding, College of Animal Science, South China Agricultural University, Guangzhou, Guangdong, People's Republic of China.
Abstract:
In the present study, we discovered that mouse oocyte maturation was inhibited by simulated microgravity via disturbing spindle organization. We cultured mouse oocytes under microgravity condition simulated by NASA's rotary cell culture system, examined the maturation rate and observed the spindle morphology (organization of cytoskeleton) during the mouse oocytes meiotic maturation. While the rate of germinal vesicle breakdown did not differ between 1 g gravity and simulated microgravity, rate of oocyte maturation decreased significantly in simulated microgravity. The rate of maturation was 8.94% in simulated microgravity and was 73.0% in 1 g gravity. The results show that the maturation of mouse oocytes in vitro was inhibited by the simulated microgravity. The spindle morphology observation shows that the microtubules and chromosomes can not form a complete spindle during oocyte meiotic maturation under simulated microgravity. And the disorder of γ-tubulin may partially result in disorganization of microtubules under simulated microgravity. These observations suggest that the meiotic spindle organization is gravity dependent. Although the spindle organization was disrupted by simulated microgravity, the function and organization of microfilaments were not pronouncedly affected by simulated microgravity. And we found that simulated microgravity induced oocytes cytoplasmic blebbing via an unknown mechanism. Transmission electron microscope detection showed that the components of the blebs were identified with the cytoplasm. Collectively, these results indicated that the simulated microgravity inhibits mouse oocyte maturation via disturbing spindle organization and inducing cytoplasmic blebbing.
Insights
Simulated microgravity significantly inhibits mouse oocyte maturation by disrupting meiotic spindle organization and causing cytoplasmic blebbing. This gravity-dependent effect impacts cytoskeleton organization crucial for cell division.
Area of Science:
- Reproductive Biology
- Cell Biology
- Space Biology
Background:
- Oocyte maturation is critical for successful reproduction.
- Understanding the effects of microgravity on reproductive cells is essential for space exploration.
- Cytoskeletal organization plays a vital role in meiosis.
Purpose of the Study:
- To investigate the impact of simulated microgravity on mouse oocyte maturation.
- To determine the effects of microgravity on meiotic spindle organization and cytoplasmic integrity.
- To elucidate the underlying mechanisms of microgravity-induced oocyte developmental failure.
Main Methods:
- Mouse oocytes were cultured under simulated microgravity using NASA's rotary cell culture system.
- Oocyte maturation rates were assessed.
- Spindle morphology and microtubule organization were observed using microscopy.
- Cytoplasmic blebbing was analyzed via transmission electron microscopy.
Main Results:
- Simulated microgravity significantly reduced the oocyte maturation rate (8.94% vs. 73.0% in 1g control).
- Microgravity disrupted meiotic spindle formation, preventing proper microtubule and chromosome alignment.
- Disorganization of gamma-tubulin was implicated in microtubule disruption.
- Microgravity induced cytoplasmic blebbing in oocytes, though microfilament organization remained largely unaffected.
Conclusions:
- Simulated microgravity inhibits mouse oocyte maturation.
- Meiotic spindle organization is gravity-dependent, with microgravity disrupting essential cytoskeletal functions.
- Cytoplasmic blebbing is a novel consequence of microgravity exposure in oocytes.
- These findings highlight potential reproductive risks associated with space travel.
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