» Articles » PMID: 36690655

Simulated Microgravity Reduces Quality of Ovarian Follicles and Oocytes by Disrupting Communications of Follicle Cells

Overview
Publisher Springer Nature
Date 2023 Jan 23
PMID 36690655
Authors
Affiliations
Soon will be listed here.
Abstract

Ovarian follicles are the fundamental structures that support oocyte development, and communications between oocytes and follicle somatic cells are crucial for oogenesis. However, it is unknown that whether exposure to microgravity influences cellular communications and ovarian follicle development, which might be harmful for female fertility. By 3D culturing of ovarian follicles under simulated microgravity (SMG) conditions in a rotating cell culture system, we found that SMG treatment did not affect the survival or general growth of follicles but decreased the quality of cultured follicles released oocytes. Ultrastructure detections by high-resolution imaging showed that the development of cellular communicating structures, including granulosa cell transzonal projections and oocyte microvilli, were markedly disrupted. These abnormalities caused chaotic polarity of granulosa cells (GCs) and a decrease in oocyte-secreted factors, such as Growth Differentiation Factor 9 (GDF9), which led to decreased quality of oocytes in these follicles. Therefore, the quality of oocytes was dramatically improved by the supplementations of GDF9 and NADPH-oxidase inhibitor apocynin. Together, our results suggest that exposure to simulated microgravity impairs the ultrastructure of ovarian follicles. Such impairment may affect female fertility in space environment.

Citing Articles

Ovarian Mechanobiology: Understanding the Interplay Between Mechanics and Follicular Development.

Wang H, Yang L Cells. 2025; 14(5).

PMID: 40072084 PMC: 11898978. DOI: 10.3390/cells14050355.


Exploring the Idea of Human Reproduction in Space: A Potential Area for Future Research.

Sharma P, Malik S, Sarkar A Cureus. 2024; 16(11):e73712.

PMID: 39677198 PMC: 11646162. DOI: 10.7759/cureus.73712.


Beyond Earth's bounds: navigating the frontiers of Assisted Reproductive Technologies (ART) in space.

Chaplia O, Mathyk B, Nichols-Burns S, Basar M, Halicigil C Reprod Biol Endocrinol. 2024; 22(1):123.

PMID: 39394617 PMC: 11468284. DOI: 10.1186/s12958-024-01290-y.


Long-term space missions' effects on the human organism: what we do know and what requires further research.

Tomsia M, Ciesla J, Smieszek J, Florek S, Macionga A, Michalczyk K Front Physiol. 2024; 15:1284644.

PMID: 38415007 PMC: 10896920. DOI: 10.3389/fphys.2024.1284644.


Omics Studies of Tumor Cells under Microgravity Conditions.

Graf J, Schulz H, Wehland M, Corydon T, Sahana J, Abdelfattah F Int J Mol Sci. 2024; 25(2).

PMID: 38255998 PMC: 10815863. DOI: 10.3390/ijms25020926.


References
1.
Zhang H, Liu L, Li X, Busayavalasa K, Shen Y, Hovatta O . Life-long in vivo cell-lineage tracing shows that no oogenesis originates from putative germline stem cells in adult mice. Proc Natl Acad Sci U S A. 2014; 111(50):17983-8. PMC: 4273382. DOI: 10.1073/pnas.1421047111. View

2.
Zhang T, He M, Zhao L, Qin S, Zhu Z, Du X . HDAC6 regulates primordial follicle activation through mTOR signaling pathway. Cell Death Dis. 2021; 12(6):559. PMC: 8164630. DOI: 10.1038/s41419-021-03842-1. View

3.
Higuchi C, Maeda Y, Horiuchi T, Yamazaki Y . A Simplified Method for Three-Dimensional (3-D) Ovarian Tissue Culture Yielding Oocytes Competent to Produce Full-Term Offspring in Mice. PLoS One. 2015; 10(11):e0143114. PMC: 4646357. DOI: 10.1371/journal.pone.0143114. View

4.
Janmey P, McCulloch C . Cell mechanics: integrating cell responses to mechanical stimuli. Annu Rev Biomed Eng. 2007; 9:1-34. DOI: 10.1146/annurev.bioeng.9.060906.151927. View

5.
Hayashi S, McMahon A . Efficient recombination in diverse tissues by a tamoxifen-inducible form of Cre: a tool for temporally regulated gene activation/inactivation in the mouse. Dev Biol. 2002; 244(2):305-18. DOI: 10.1006/dbio.2002.0597. View