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Menstrual blood-derived stem cell exosomes improve ovarian function in chemotherapy-Induced POF rats via apoptosis regulation
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  • Published: 13 March 2026

Menstrual blood-derived stem cell exosomes improve ovarian function in chemotherapy-Induced POF rats via apoptosis regulation

  • Xianying Cheng1 na1,
  • Yanqin Wu1 na1,
  • Li Cheng2 na1,
  • Minjie Liu3,
  • Kwanghann Gan1,
  • Yuanyuan Wang4,
  • Ting Zhang5,
  • Lingqiao Yang6,
  • Yige Wang7,
  • Liya Xu1 &
  • …
  • Zhenyu Xu7 

Scientific Reports , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Medical research
  • Stem cells

Abstract

Recent studies have demonstrated that exosome therapy can promote the recovery of ovaries in premature ovarian failure (POF) models, which may aid in fertility restoration. This study aimed to investigate the therapeutic efficacy of exosomes derived from menstrual blood-derived mesenchymal stem cells (MenSCs-Exos) in a POF rat model, exploring its underlying mechanisms and detecting the optimal effective therapeutic dose. A POF model was established by an alkylating agent cyclophosphamide (CTX). All POF rats were divided into four groups (eight rats per group) and received a single intervention via the tail vein: phosphate-buffered saline (PBS), low-dose MenSCs-Exos (0.5 mL), middle-dose MenSCs-Exos (1 mL), high-dose MenSCs-Exos (2.0 mL). The concentration of MenSCs-Exos was 1 × 109 particles/mL. Serum was collected from the tail vein before CTX injection and on the 14th day after MenSCs-Exos treatment to measure the serum levels of follicle-stimulating hormone (FSH), luteinizing hormone (LH), anti-Müllerian hormone (AMH), and estradiol (E2) via ELISA. The ovarian pathology and follicle counts were examined by H&E. The protein expression and concentration of B-cell lymphoma-2(Bcl-2) and Bcl-2 associated X protein (Bax) in ovarian tissue were examined by western blot and ELISA. Rats in the middle- and high-dose MenSCs-Exos groups recovered their physical condition after treatment, and their body weight was significantly higher than that of the placebo group but lower than that of the control group, respectively ( P < 0.05). Compared to the placebo group, serum E2 and AMH levels were significantly increased, while serum FSH and LH levels were decreased (P < 0.05). MenSCs-Exos treatment also improved ovarian tissue morphology, and the number of follicles at all stages was markedly increased compared with those in the placebo group ( P < 0.05). In addition, the expression of anti-apoptotic Bcl-2 protein was significantly up-regulated and the expression of pro-apoptotic Bax protein was markedly inhibited after treatment, and the Bcl-2/Bax ratio was also significantly increased ( P < 0.05). Finally, the middle-dose achieved optimal therapeutic effect among the three MenSCs-Exos groups, as the low-dose achieved a less effective outcome and the high-dose exerted no additional therapeutic effects. MenSCs-Exos transplantation could effectively restore ovarian function and promote ovarian regeneration in Chemotherapy-induced POF model, whose mechanism is mainly associated with the regulation of apoptotic-related proteins expression. Additionally, the effective dose is middle-dose MenSCs-Exos (1 mL) or 1 × 109 particles in POF rats. Nevertheless, all these findings require further clinical validation in human models.

Data availability

The data that support the findings of this study are available from the corresponding author, Zhen-Yu Xu, upon reasonable request.

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Acknowledgements

We are grateful to Yong He for animal experiment technical guidance.

Funding

This study was supported by grants from the National Key R&D Program of China grant (No. 2022YFC2304405 and 2022YFA1105603); Zhejiang Provincial Key Research and Development Program (No. 2019C03015); Hangzhou Health Science and Technology Plan Project(No. B20220020); Medical and Health Technology Plan Project in Gongshu District, Hangzhou, Zhejiang Province(No. A202208); Zhejiang Province Traditional Chinese Medicine Technology Plan Project(No. 2023ZL591); the Key laboratory& Women’s Hospital, Zhejiang University School of Medicine (No. ZDFY2022-RG-4). The funders played no role in the design and implementation of the study, data analysis, drafting the manuscript or the decision to submit the manuscript for publication.

Author information

Author notes
  1. These are contributed equally to this work: Xianying Cheng, Yanqin Wu and Li Cheng.

Authors and Affiliations

  1. Department of Obstetrics and Gynecology, Shulan (Hangzhou) Hospital, Shulan International Medical College, Zhejiang Shuren University, Hangzhou, 310022, China

    Xianying Cheng, Yanqin Wu, Kwanghann Gan & Liya Xu

  2. Department of Obstetrics and Gynecology, Hangzhou Xixi Hospital, Hangzhou, 310023, China

    Li Cheng

  3. Clinical Laboratory, Shulan (Hangzhou) Hospital, Shulan International Medical College, Zhejiang Shuren University, Hangzhou, 310022, China

    Minjie Liu

  4. Department of Obstetrics and Gynecology, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, 310015, China

    Yuanyuan Wang

  5. Department of Pathology, Shulan (Hangzhou) Hospital, Shulan International Medical College, Zhejiang Shuren University, Hangzhou, 310022, China

    Ting Zhang

  6. Cellular Therapy Drugs R&D Center, Innovative Precision Medicine (IPM) Group, Hangzhou, 311217, China

    Lingqiao Yang

  7. Cellular Therapy Drugs Innovation Research Institute, Innovative Precision Medicine (IPM) Group, Hangzhou, 311217, China

    Yige Wang & Zhenyu Xu

Authors
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Contributions

All authors contributed to the study conception and design. XY CHENG, YQ W and LC conducted the experiments; ZY XU, LQ YANG and LY XU prepared the exosomes; MJ LIU performed blot and ELISA; TZ conducted HE staining and histological analysis; YY WANG and GH YANG collected and analyzed the data; YG WANG provided technical and writing guidance; XY CHENG and ZY XU prepared the manuscript for publication and reviewed the draft of the manuscript. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Liya Xu or Zhenyu Xu.

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The authors declare no competing interests.

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Cheng, X., Wu, Y., Cheng, L. et al. Menstrual blood-derived stem cell exosomes improve ovarian function in chemotherapy-Induced POF rats via apoptosis regulation. Sci Rep (2026). https://doi.org/10.1038/s41598-026-43562-0

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  • Received: 25 March 2025

  • Accepted: 05 March 2026

  • Published: 13 March 2026

  • DOI: https://doi.org/10.1038/s41598-026-43562-0

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Keywords

  • Premature ovarian failure
  • Chemotherapy
  • Menstrual blood-derived mesenchymal stem cells
  • Exosomes
  • Rat model
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