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DOI 10.1038/s41598-024-65134-w

Медицинская библиотека · Scientific reports · 2024

A side-by-side comparison of different capacitation media in developing mouse sperm fertilizing ability.

González Lucas N, Giaccagli María M, Herzfeld Jael D, Cuasnicú Patricia S, Da Ros Vanina G, Cohen Débora J

СтатьяСравнительное исследованиеПеревод пока не подготовлен

Аннотация

To acquire the ability to fertilize the egg, mammalian spermatozoa must undergo a series of changes occurring within the highly synchronized and specialized environment of the female reproductive tract, collectively known as capacitation. In an attempt to replicate this process in vitro, various culture media for mouse sperm were formulated over the past decades, sharing a similar overall composition but differing mainly in ion concentrations and metabolic substrates. The widespread use of the different media to study the mechanisms of capacitation might hinder a comprehensive understanding of this process, as the medium could become a confounding variable in the analysis. In this context, the present side-by-side study compares the influence of four commonly used culture media (FD, HTF and two TYH versions) on mouse sperm capacitation. We evaluated the induction of protein kinase A phosphorylation pathway, motility, hyperactivation and acrosome reaction. Additionally, in vitro fertilization and embryo development were also assessed. By analyzing these outcomes in two mouse colonies with different reproductive performance, our study provides critical insights to improve the global understanding of sperm function. The results obtained highlight the importance of considering variations in medium composition, and their potential implications for the future interpretation of results.

Для цитирования: González Lucas N, Giaccagli María M, Herzfeld Jael D, Cuasnicú Patricia S, Da Ros Vanina G, Cohen Débora J. A side-by-side comparison of different capacitation media in developing mouse sperm fertilizing ability.. Scientific reports. 2024. DOI: 10.1038/s41598-024-65134-w.

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