The intrinsic impact of mechanical stress on the maintenance of oocyte dormancy

In the mammalian ovary, most oocytes remain dormant, and their dormant status plays a central role in maintaining the reservoir population of the female germ line. The equilibrium between the dormant and active states, the latter of which is responsible for producing mature oocytes, is therefore crucial for ensuring the sustained reproductive capability of females. We have previously reported that mechanical stress in the ovary plays a crucial role in oocyte dormancy. However, the mechanism underlying this relation remains unclear. Here, we demonstrated that the mechanical stress is directly transduced into the oocytes, rather than to the surrounding granulosa cells. Culture experiments and live-imaging analysis revealed the nuclear localization of FOXO3, a hallmark of oocyte dormancy, within oocytes cultured alone in response to mechanical stress. Interestingly, we found that the cytological response to mechanical stress was accompanied by ligand-independent internalization of the c-kit receptor, which dampens intracellular signaling and prevents oocyte activation. These results shed light on the relation between mechanical stress and oocyte dormancy and provide clues toward a greater understanding of female reproductive capability.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-01-16
DOI
https://doi.org/10.1073/pnas.2526249123
Primary Topic
Reproductive Biology and Fertility
Type
article
Field-Weighted Citation Impact
0.00

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article

The intrinsic impact of mechanical stress on the maintenance of oocyte dormancy

Kenjiro Shirane, Yuzuru Kato, Norio Hamada, Hiroko Nakamura et al.
Proceedings of the National Academy of Sciences
Reproductive Biology and Fertility
article

The intrinsic impact of mechanical stress on the maintenance of oocyte dormancy

Kenjiro Shirane, Yuzuru Kato, Norio Hamada, Hiroko Nakamura, Go Nagamatsu, K. Kato, Katsuhiko Hayashi, Hiroshi Kimura
article en

Abstract

In the mammalian ovary, most oocytes remain dormant, and their dormant status plays a central role in maintaining the reservoir population of the female germ line. The equilibrium between the dormant and active states, the latter of which is responsible for producing mature oocytes, is therefore crucial for ensuring the sustained reproductive capability of females. We have previously reported that mechanical stress in the ovary plays a crucial role in oocyte dormancy. However, the mechanism underlying this relation remains unclear. Here, we demonstrated that the mechanical stress is directly transduced into the oocytes, rather than to the surrounding granulosa cells. Culture experiments and live-imaging analysis revealed the nuclear localization of FOXO3, a hallmark of oocyte dormancy, within oocytes cultured alone in response to mechanical stress. Interestingly, we found that the cytological response to mechanical stress was accompanied by ligand-independent internalization of the c-kit receptor, which dampens intracellular signaling and prevents oocyte activation. These results shed light on the relation between mechanical stress and oocyte dormancy and provide clues toward a greater understanding of female reproductive capability.

Proceedings of the National Academy of SciencesVol. 123(3)
Kyushu University (JP), Ube Frontier University (JP), Osaka University of Human Sciences (JP), Japan Science and Technology Agency (JP), Kai Research (United States) (US), University of Yamanashi (JP), The University of Osaka (JP)
Open Philanthropy Project, Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science, Japan Science and Technology Agency, Precursory Research for Embryonic Science and Technology
Gender equality
Openalex Percentile: Top 87%
Reproductive Biology and Fertility
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