Characterization of subsets of human spermatozoa at different stages of maturation: implications in the diagnosis and treatment of male infertility
Abstract
Background Reactive oxygen species (ROS)-induced damage of membrane phospholipids and DNA in human spermatozoa has been implicated in the pathogenesis of male infertility. In this study, variations in ROS production, DNA structure (as measured by the sperm chromatin structure assay) and lipid composition, were studied in human spermatozoa at different stages of maturation. Methods Sperm subsets were isolated by discontinuous density gradient centrifugation of semen samples obtained from healthy donors and from infertility patients. Results DNA damage and ROS production were highest in immature spermatozoa with cytoplasmic retention and abnormal head morphology, and lowest in mature spermatozoa. Docosahexaenoic acid and sterol content were highest in immature germ cells and immature spermatozoa, and lowest in mature spermatozoa. The relative proportion of ROS-producing immature spermatozoa in the sample was directly correlated with DNA damage in mature spermatozoa, and inversely correlated with the recovery of motile spermatozoa. There was no correlation between DNA damage and sperm morphology in mature spermatozoa. Conclusions The high levels of ROS production and DNA damage observed in immature spermatozoa may be indicative of derangements in the regulation of spermiogenesis. DNA damage in mature spermatozoa may be the result of oxidative damage by ROS-producing immature spermatozoa during sperm migration from the seminiferous tubules to the epididymis.
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During sperm migration to the epididymis, the ROS from immature spermatozoa cause oxidative and DNA damage to the mature spermatozoa.
“During sperm migration to the epididymis, the ROS from immature spermatozoa will cause oxidative and DNA damage to the mature spermatozoa (77).”
From Isolated teratozoospermia: revisiting its relevance in male infertility: a narrative review (2024) · cites this paper as [77]
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Should we evaluate and treat sperm DNA fragmentation?
Agarwal, A., Cho, C.-L., & Esteves, S. C. (2016) · Current Opinion in Obstetrics & Gynecology · doi:10.1097/gco.0000000000000271 · Cited by 148 · see citing works
Self-citationIsolated teratozoospermia: revisiting its relevance in male infertility: a narrative review
Atmoko, W., Savira, M., Shah, R., Chung, E., & Agarwal, A. (2024) · Translational Andrology and Urology · doi:10.21037/tau-23-397 · Cited by 23 · see citing works
“During sperm migration to the epididymis, the ROS from immature spermatozoa will cause oxidative and DNA damage to the mature spermatozoa (77).”
Self-citation
- Authors
- Ollero, M., Gil-Guzman, E., Lopez, M. C., Sharma, R. K., Agarwal, A., Larson, K., Evenson, D., Thomas, A. J., & Alvarez, J. G.
- Affiliations
- Beth Israel Deaconess Medical Center (US)
- Cleveland Clinic (US)
- Harvard University (US)
- South Dakota State University (US)
- Venue
- Human Reproduction
- Publisher
- Oxford University Press (OUP)
- Published
- 2001-09
- Volume
- 16
- Issue
- 9
- Pages
- 1912-1921
- ISSN
- 0268-1161 (ISSN-L)
- 1460-2350
- OpenAlex
- W2122237205
- Cited by
- 392
- References
- 0
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 7 · 2023: 11 · 2022: 15 · 2021: 21 · 2020: 20 · 2019: 15 · 2018: 13 · 2017: 19 · 2016: 13 · 2015: 14 · 2014: 15 · 2013: 27 · 2012: 30
- FWCI
- 17.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Human Reproduction (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Foundation
- Cleveland Clinic Foundation
- Baxter Healthcare Corporation
- Topics
- Health Sciences › Medicine › Reproductive Medicine › Sperm and Testicular Function
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Reproductive Biology and Fertility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Reproductive biology and impacts on aquatic species
- Keywords
- sperm maturation, male infertility, reactive oxygen species, sperm DNA damage, sperm chromatin structure assay, sperm lipid composition, docosahexaenoic acid, sterols, sperm motility, sperm morphology, spermiogenesis, oxidative stress, epididymis
- MeSH terms
- Chromatin, DNA, DNA Damage, Docosahexaenoic Acids, Humans, Infertility, Male, Male, Reference Values, Sperm Count, Sperm Motility, Spermatozoa, Sterols, Cellular Senescence, Reactive Oxygen Species
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