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Updated: Jun 24, 2026

The Examination of Peroxidase-Positive Leukocytes in Semen
Published on: January 19, 2024
alpha1-antitrypsin prevents polymorphonuclear leucocyte-elastase effects on spermatozoa quality
J Lessig1, J Arnhold, H-J Glander
1Institute of Medical Physics and Biophysics, Medical Faculty, University of Leipzig, Leipzig, Germany. jacqueline.lessig@medizin.uni-leipzig.de
Abstract:
Elevated levels of polymorphonuclear leucocyte (PMN)-derived elastase, which is suggested as marker for inflammations in the male genital tract, correlate well with spermatozoa deterioration. PMN elastase caused a time- and concentration-dependent (up to a elastase concentration of 0.5 microg/mL) externalization of phosphatidylserine and intercalation of propidium iodide on human spermatozoa. There are apparently a limited number of target sites for elastase on spermatozoa surface, because the further enhancement of elastase amount did not fasten alterations in spermatozoa parameters. Analysis of flow cytometry data revealed that most spermatozoa were in a necrotic state after an exposure with elastase for 22 h. Some apoptotic cells were only detected at shorter incubation periods. Seminal plasma prevented in a concentration-dependent manner the PMN elastase-mediated loss of vitality of spermatozoa. We detected by blotting techniques large amounts of alpha(1)-antitrypsin in seminal plasma. This antiproteinase is known to inactivate elastase at inflammatory sites. Increasing concentrations of alpha(1)-antitrypsin prevented gradually spermatozoa deterioration induced by elastase. Thus, alpha(1)-antitrypsin contributes to an efficient protease/antiproteinase balance in seminal plasma. A disturbed balance will promote the development of chronic inflammations which can also be the reason for male infertility problems.
Insights
Polymorphonuclear leucocyte (PMN)-derived elastase damages sperm, but seminal plasma
Area of Science:
- Reproductive Biology
- Immunology
- Andrology
Background:
- Inflammation in the male genital tract is linked to sperm damage.
- Polymorphonuclear leucocyte (PMN)-derived elastase is a key marker of such inflammation.
- Spermatozoa deterioration correlates with elevated PMN elastase levels.
Purpose of the Study:
- To investigate the effects of PMN elastase on human spermatozoa.
- To determine the protective role of seminal plasma components against elastase-induced sperm damage.
- To elucidate the contribution of alpha(1)-antitrypsin to seminal plasma's protective capacity.
Main Methods:
- Human spermatozoa were exposed to varying concentrations and durations of PMN elastase.
- Flow cytometry was used to assess phosphatidylserine externalization and propidium iodide uptake.
- Blotting techniques identified alpha(1)-antitrypsin in seminal plasma.
- Sperm vitality assays were performed with and without seminal plasma and alpha(1)-antitrypsin.
Main Results:
- PMN elastase induced time- and concentration-dependent sperm damage, leading to necrosis and apoptosis.
- Seminal plasma demonstrated a concentration-dependent protective effect against elastase-induced sperm damage.
- Alpha(1)-antitrypsin was identified in seminal plasma and its increasing concentrations progressively inhibited elastase-mediated sperm deterioration.
- A protease/antiproteinase balance, involving alpha(1)-antitrypsin, is crucial for maintaining sperm vitality.
Conclusions:
- PMN elastase significantly impairs sperm function and viability.
- Seminal plasma, particularly alpha(1)-antitrypsin, plays a vital protective role against inflammatory damage to spermatozoa.
- Imbalances in the seminal protease/antiproteinase system may contribute to male infertility.
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