Metabolic characterization of human sperm cells using the Seahorse metabolic flux analyzer

Background The concerning trend on male infertility global prevalence, together with the unexplainable causes in half of those cases, highlights that there are still aspects of this disease to be understood and solved. To address this issue, one should not only be aware of the limitations of the imp...

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Bibliographic Details
Published in:Andrology (Oxford) 2024-02, Vol.12 (2), p.410-421
Main Authors: Freitas‐Martins, Artur, Sousa, Maria Inês, Cristo, Maria Inês, Ramalho‐Santos, João, Amaral, Sandra
Format: Article
Language:English
Subjects:
human sperm cell
Infertility
Metabolism
Seahorse metabolic flux analyzer
Sperm
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Summary:Background The concerning trend on male infertility global prevalence, together with the unexplainable causes in half of those cases, highlights that there are still aspects of this disease to be understood and solved. To address this issue, one should not only be aware of the limitations of the implemented diagnostic tools, but also understand the sperm cell in depth, structurally, biochemically, molecularly in order to develop reliable and ready‐to‐be new/improved diagnostic tools. In this sense, the sperm cells metabolism, highly related to its functionality, seems to be a promising aspect to explore. Though there is much information on the human sperm metabolism, there is still a lack of a quick integrated and comprehensive analysis that may be introduced with the potential to reveal innovative clinically relevant information. Objectives Find metabolic details on human sperm that can be accessed easily, in real time and using few cells, relying on the bivalent potential of the Seahorse flux analyzer (SFA). Results We have obtained standard records on human sperm cells’ oxygen consumption rate (OCR) and extracellular acidification rate (ECAR), that together with the metabolic metrics provided information on sperm cells’ oxidative and glycolytic metabolism. Furthermore, a metabolic interindividual variation was observed. Discussion and conclusion Although the comparison with other species or cell types is not linear and warrant further studies, the metabolic profile of human sperm cells seems to be similar to that of other species. Altogether our results corroborate the value of SFA for metabolic human sperm cell analysis, warranting new studies, and anticipating several applications in the male infertility field.
ISSN:2047-2919
2047-2927
DOI:10.1111/andr.13486