Evidence map›Paper›PMID 41437196›Full record

ArticleClinical and experimental reproductive medicine2026

Rapamycin preserves primordial follicles during closed‑system vitrification of mouse ovarian tissue.

Yuji Tanaka, Akie Takebayashi, Mari Deguchi, Tsukuru Amano, Akiko Nakamura, Ayako Inatomi, Shunichiro Tsuji, Takashi Murakami

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Article in Clinical and experimental reproductive medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yuji TanakaDepartment of Obstetrics and Gynecology, Shiga University of Medical Science, Otsu, Japan. yujit@belle.shiga-med.ac.jp.
Akie TakebayashiDepartment of Obstetrics and Gynecology, Shiga University of Medical Science, Otsu, Japan.
Mari DeguchiDepartment of Obstetrics and Gynecology, Shiga University of Medical Science, Otsu, Japan.
Tsukuru AmanoDepartment of Obstetrics and Gynecology, Shiga University of Medical Science, Otsu, Japan.
Akiko NakamuraDepartment of Obstetrics and Gynecology, Shiga University of Medical Science, Otsu, Japan.
Ayako InatomiDepartment of Obstetrics and Gynecology, Shiga University of Medical Science, Otsu, Japan.
Shunichiro TsujiDepartment of Obstetrics and Gynecology, Shiga University of Medical Science, Otsu, Japan.
Takashi MurakamiDepartment of Obstetrics and Gynecology, Shiga University of Medical Science, Otsu, Japan.

Funding

Japan Society for the Promotion of Science 24K12551
6 · The paper itself

Abstract

objectiveOvarian tissue cryopreservation is an essential fertility preservation technique. Two primary methods are used for ovarian tissue cryopreservation: slow freezing and vitrification. Recently, vitrification has been favored over slow freezing, and a closed system is recommended to prevent cross-contamination in liquid nitrogen. Follicular loss during freezing and thawing remains a major challenge. We investigated whether rapamycin, an inhibitor of the mechanistic target of rapamycin (mTOR) pathway, could mitigate primordial follicle loss during closed-system vitrification and thawing of mouse ovarian tissue.

methodsMouse ovaries were vitrified and thawed with or without 750 nanomolar rapamycin, then immediately analyzed or cultured for 5 days. Activation of the mTOR pathway was assessed using phosphorylated S6 kinase immunostaining, and follicle survival and development were evaluated by histological analysis.

resultsClosed-system vitrification did not induce apoptosis in primordial follicles. The median phosphorylated S6K-positive rate in primordial follicles was 7.1% in fresh controls, 87.9% in the rapamycin-free group, and 19.0% in the rapamycin-treated group (fresh-control vs. rapamycin-free and rapamycin-free vs. rapamycin-treated, both p<0.001). Rapamycin treatment suppressed this activation, resulting in significantly higher primordial follicle counts after culture (605 vs. 289 follicles per ovary, p<0.05) and a lower ratio of primary to primordial follicles, indicating reduced follicle activation.

conclusionThese findings demonstrate that rapamycin preserves the primordial follicle pool by preventing follicle activation during cryopreservation and thawing. Incorporating rapamycin into closed-system vitrification protocols may improve ovarian tissue cryopreservation outcomes and enhance fertility preservation for patients with cancer.

Indexed as

CryopreservationFertility preservationOvarySirolimusTOR serine-threonine kinasesVitrification

Identifiers

PMID41437196
PMCPMC13541409

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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.