Evidence map›Paper›PMID 38650029›Full record

ArticleStem cell research & therapy2024

Mesenchymal stem cells promote ovarian reconstruction in mice.

Jiazhao Li, Haonan Fan, Wei Liu, Jing Zhang, Yue Xiao, Yue Peng, Weijie Yang, Wenwen Liu, Yuanlin He, Lianju Qin and 2 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.3field-weighted citation impact, top 6% of its field
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

12 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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  8. Mechanistic study on the role of multi-pathway autophagy in ovarian aging: literature review.Apoptosis : an international journal on programmed cell death · 2025
    Review
  9. Review
  10. Review
  11. Article
  12. Application of adult stem cells in obstetrics and gynecology: A scoping review.European journal of obstetrics & gynecology and reproductive biology: X · 2025
    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

12 authors at 7 institutions in 1 country.

Jiazhao LiState Key Laboratory of Reproductive Medicine and Offspring health, Nanjing Medical University, 210029, Nanjing, China.
Haonan FanState Key Laboratory of Reproductive Medicine and Offspring health, Nanjing Medical University, 210029, Nanjing, China.
Wei LiuState Key Laboratory of Reproductive Medicine and Offspring health, Nanjing Medical University, 210029, Nanjing, China.
Jing ZhangState Key Laboratory of Reproductive Medicine and Offspring health, Nanjing Medical University, 210029, Nanjing, China.
Yue XiaoState Key Laboratory of Reproductive Medicine and Offspring health, Nanjing Medical University, 210029, Nanjing, China.
Yue PengState Key Laboratory of Reproductive Medicine and Offspring health, Nanjing Medical University, 210029, Nanjing, China.
Weijie YangState Key Laboratory of Reproductive Medicine and Offspring health, Nanjing Medical University, 210029, Nanjing, China.
Wenwen LiuState Key Laboratory of Reproductive Medicine and Offspring health, Nanjing Medical University, 210029, Nanjing, China.
Yuanlin HeState Key Laboratory of Reproductive Medicine and Offspring health, Nanjing Medical University, 210029, Nanjing, China.
Lianju QinState Key Laboratory of Reproductive Medicine and Offspring Health, Center of Clinical Reproductive Medicine, Jiangsu Province Hospital, The First Affiliated Hospital of Nanjing Medical University, 210029, Nanjing, China. ljqin@njmu.edu.cn.
Xiang MaState Key Laboratory of Reproductive Medicine and Offspring Health, Center of Clinical Reproductive Medicine, Jiangsu Province Hospital, The First Affiliated Hospital of Nanjing Medical University, 210029, Nanjing, China. sxmaxiang@126.com.
Jing LiState Key Laboratory of Reproductive Medicine and Offspring health, Nanjing Medical University, 210029, Nanjing, China. ljwth@njmu.edu.cn.ORCID 0000-0001-8692-4981
Nanjing Medical University · CNJiangsu Province Hospital · CNNanjing Maternity and Child Health Care Hospital · CNWannan Medical College · CNFirst Affiliated Hospital Zhejiang University · CNKingmed Diagnostics · CNSir Run Run Shaw Hospital · CN

Funding

Jiangsu Provincial Science and Technology Department Social Development Surface Program BE2021743the National Key Research and Development Program of China 2022YFC2703000the Wuhu Science and Technology Program 2021cg34
6 · The paper itself

Abstract

backgroundStudies have shown that chemotherapy and radiotherapy can cause premature ovarian failure and loss of fertility in female cancer patients. Ovarian cortex cryopreservation is a good choice to preserve female fertility before cancer treatment. Following the remission of the disease, the thawed ovarian tissue can be transplanted back and restore fertility of the patient. However, there is a risk to reintroduce cancer cells in the body and leads to the recurrence of cancer. Given the low success rate of current in vitro culture techniques for obtaining mature oocytes from primordial follicles, an artificial ovary with primordial follicles may be a good way to solve this problem.

methodsIn the study, we established an artificial ovary model based on the participation of mesenchymal stem cells (MSCs) to evaluate the effect of MSCs on follicular development and oocyte maturation. P2.5 mouse ovaries were digested into single cell suspensions and mixed with bone marrow derived mesenchymal stem cells (BM-MSCs) at a 1:1 ratio. The reconstituted ovarian model was then generated by using phytohemagglutinin. The phenotype and mechanism studies were explored by follicle counting, immunohistochemistry, immunofluorescence, in vitro maturation (IVM), in vitro fertilization (IVF), real-time quantitative polymerase chain reaction (RT-PCR), and Terminal-deoxynucleotidyl transferase mediated nick end labeling(TUNEL) assay.

resultsOur study found that the addition of BM-MSCs to the reconstituted ovary can enhance the survival of oocytes and promote the growth and development of follicles. After transplanting the reconstituted ovaries under kidney capsules of the recipient mice, we observed normal folliculogenesis and oocyte maturation. Interestingly, we found that BM-MSCs did not contribute to the formation of follicles in ovarian aggregation, nor did they undergo proliferation during follicle growth. Instead, the cells were found to be located around growing follicles in the reconstituted ovary. When theca cells were labeled with CYP17a1, we found some overlapped staining with green fluorescent protein(GFP)-labeled BM-MSCs. The results suggest that BM-MSCs may participate in directing the differentiation of theca layer in the reconstituted ovary.

conclusionsThe presence of BM-MSCs in the artificial ovary was found to promote the survival of ovarian cells, as well as facilitate follicle formation and development. Since the cells didn't proliferate in the reconstituted ovary, this discovery suggests a potential new and safe method for the application of MSCs in clinical fertility preservation by enhancing the success rate of cryo-thawed ovarian tissues after transplantation.

Indexed as

Mesenchymal Stem CellsOocytesOvaryAnimalsFemaleMesenchymal Stem Cell TransplantationMiceOvarian FollicleArtificial ovaryFertility preservationMesenchymal stem cells

Identifiers

PMID38650029
PMCPMC11036642
OpenAlexW4395013420

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.