Evidence map›Paper›PMID 41543895›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

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

Go Nagamatsu, Kenjiro Shirane, Yuzuru Kato, Hiroko Nakamura, Norio Hamada, Kiyoko Kato, Hiroshi Kimura, Katsuhiko Hayashi

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Mechanics of compression-driven morphogenesis.Development (Cambridge, England) · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Go NagamatsuDepartment of Stem Cell Biology and Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.ORCID 0000-0002-4901-8514
Kenjiro ShiraneDepartment of Stem Cell Biology and Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.
Yuzuru KatoDepartment of Genome Biology, Graduate School of Medicine, Osaka University, Suita, Osaka 565-0871, Japan.
Hiroko NakamuraDivision of Medical Engineering Collaboration for Medical Research, Micro/Nano Technology Center, Tokai University, Kanagawa 259-1292, Japan.
Norio HamadaDepartment of Obstetrics and Gynecology, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.ORCID 0000-0002-0906-8277
Kiyoko KatoDepartment of Obstetrics and Gynecology, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.ORCID 0000-0003-0047-7637
Hiroshi KimuraDivision of Medical Engineering Collaboration for Medical Research, Micro/Nano Technology Center, Tokai University, Kanagawa 259-1292, Japan.
Katsuhiko HayashiDepartment of Stem Cell Biology and Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.ORCID 0000-0002-2479-2941

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 23H04947MEXT | Japan Society for the Promotion of Science (JSPS) 23H04949MEXT | Japan Society for the Promotion of Science (JSPS) 23K18078MEXT | Japan Society for the Promotion of Science (JSPS) 23K18137MEXT | Japan Society for the Promotion of Science (JSPS) 23K20043MEXT | Japan Society for the Promotion of Science (JSPS) 24H00059MEXT | Japan Society for the Promotion of Science (JSPS) 24H02040Open Philanthropy Project N/ATakeda Science Foundation (TSF) N/A
6 · The paper itself

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.

Indexed as

OocytesStress, MechanicalAnimalsFemaleForkhead Box Protein O3Forkhead Transcription FactorsGranulosa CellsMiceProto-Oncogene Proteins c-kitSignal TransductionForkhead Box Protein O3Forkhead Transcription FactorsFoxO3 protein, mouseProto-Oncogene Proteins c-kitFOXO3oocyteovary

Identifiers

PMID41543895
PMCPMC12818438

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.