Advancements in Spermatogenesis In Vitro: From Murine Success to Human Applications
Kamoshita M.
Narrative Review on Face & Skin, published in Reprod Med Biol (2026) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Narrative Review
- Journal
- Reprod Med Biol (2026)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 41937972
- PMCID
- PMC13045498
- DOI
- 10.1002/rmb2.70044
Abstract (original English)
Background Male infertility due to spermatogenic failure remains a global challenge. While in vitro spermatogenesis (IVS) offers potential for fertility preservation, recapitulating the complex, species-specific testicular niche remains a formidable task. This review evaluates IVS progress and bottlenecks across rodents, primates, domestic animals, and humans. Methods This review summarizes a comprehensive literature synthesis of IVS methodologies, including organ culture, microfluidics, 3D organoids, and induced pluripotent stem cell (iPSC)-derived systems. Particular focus was placed on the technical evolution from the foundational gas-liquid interface method to the development of bioengineering platforms. Main findings Murine IVS systems have successfully and consistently produced fertile offspring. Conversely, human and non-human primate models show meiotic arrest, with differentiation typically stagnating at pre-meiotic stages. Although domestic animal models have occasionally yielded haploid cells, efficiency remains low. Recent single-cell analyses suggest that disrupted somatic-germ cell communication is a key driver of these failures. Conclusion Bridging the gap between rodent success and human application requires integrating developmental biology with precision engineering. Future efforts must focus on establishing rigorous epigenetic and functional validation to ens
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is a narrative review: it collects no new patient data and does not systematically appraise evidence quality.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
How we grade evidenceBrowse all related research
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