Evidence map›Paper›PMID 39753886›Full record

ArticleScientific reports2025

Development of the membrane ceiling method for in vitro spermatogenesis.

Maki Kamoshita, Hiroki Shirai, Hiroko Nakamura, Tetsuya Kishimoto, Yuki Hatanaka, Daisuke Mashiko, Katsuhiro Esashika, Jingjing Yang, Satoshi Yamasaki, Takehiko Ogawa and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Sperm and offspring production in a nonobstructive azoospermia mouse model via testicular mRNA delivery using lipid nanoparticles.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Review
  7. 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.

Maki KamoshitaResearch Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Hiroki ShiraiMicro/Nano Technology Center, Tokai University, Kanagawa, Japan.
Hiroko NakamuraMicro/Nano Technology Center, Tokai University, Kanagawa, Japan.
Tetsuya KishimotoMicro/Nano Technology Center, Tokai University, Kanagawa, Japan.
Yuki HatanakaImmunology Frontier Research Center, Osaka University, Osaka, Japan.
Daisuke MashikoImmunology Frontier Research Center, Osaka University, Osaka, Japan.
Katsuhiro EsashikaBiotechnology Department, Synthetic Chemicals Laboratory, R&D Center, Mitsui Chemicals, Inc, Chiba, Japan.
Jingjing YangMarketing & Innovation Department, New Business Incubation Center, Mitsui Chemicals, Inc, Tokyo, Japan.
Satoshi YamasakiMarketing & Innovation Department, New Business Incubation Center, Mitsui Chemicals, Inc, Tokyo, Japan.
Takehiko OgawaInstitute of Molecular Medicine and Life Science, Yokohama City University, Kanagawa, Japan.
Hiroshi KimuraMicro/Nano Technology Center, Tokai University, Kanagawa, Japan. hkimura@tokai.ac.jp.
Masahito IkawaResearch Institute for Microbial Diseases, Osaka University, Osaka, Japan. ikawa@biken.osaka-u.ac.jp.

Funding

Bill & Melinda Gates Foundation grant INV001902Gates Foundation INV-001902Japan Agency for Medical Research and Development JP22be1004201Japan Agency for Medical Research and Development JP23jf0126001Japan Science and Technology Agency grant JPMJCR21N1Japan Society for the Promotion of Science JP21H05033Japan Society for the Promotion of Science JP22K15030Japan Society for the Promotion of Science JP24K01321
6 · The paper itself

Abstract

Spermatogenesis is one of the most complex processes of cell differentiation and its failure is a major cause of male infertility. Therefore, a proper model that recapitulates spermatogenesis in vitro has been long sought out for basic and clinical research. Testis organ culture using the gas-liquid interphase method has been shown to support spermatogenesis in mice and rats. However, the conventional method using agarose gel has limitations including medium replacement efficiency and live imaging because agarose absorbs medium and is not transparent. To overcome this issue, we developed a new device using microporous membranes and oxygen-permeable materials. Mouse testes sandwiched between a microporous polyethylene terephthalate (PET) membrane on top and an oxygen-permeable 4-polymethyl-1-pentene polymer (PMP) membrane base maintained spermatogenesis over months. The chamber volume was minimized to 0.1% of the culture medium. Weekly time-lapse live imaging enabled us to observe transgenically fluorescent acrosome and nuclear shape formation throughout spermatogenesis. Finally, we obtained healthy fertile offspring from spermatozoa generated in our system. The device could be used not only for basic research to understand spermatogenesis but also for applied research, such as diagnosing and treating male infertility.

Indexed as

SpermatogenesisAnimalsMaleMembranes, ArtificialMiceOrgan Culture TechniquesPolyethylene TerephthalatesSpermatozoaTestisMembranes, ArtificialPolyethylene Terephthalates4-Polymethyl-1-pentene polymer (PMP)Fluorinated ethylene-propylene copolymer (FEP)In vitro spermatogenesisMembrane ceiling chipPolydimethylsiloxane (PDMS)Testis culture

Identifiers

PMID39753886
PMCPMC11699200

What OpenQuestion holds

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Registered trials

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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.