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Activation of polymorphonuclear leukocytes by spermatozoa
Archives of Andrology
|January 1, 1985
Summary
Human sperm activate immune cells called polymorphonuclear leukocytes (PMN) via the complement system. Dead sperm were more effective activators than live sperm, highlighting a role for complement activation in immune responses.
Area of Science:
- Immunology
- Reproductive Biology
- Complement System
Background:
- Human spermatozoa can interact with and activate immune cells.
- Polymorphonuclear leukocytes (PMN) are key immune cells involved in inflammatory responses.
- The complement system is a crucial part of innate immunity, involving various proteins and pathways.
Purpose of the Study:
- To investigate the mechanism by which human spermatozoa activate PMN.
- To determine the role of serum components, including antibodies and complement, in sperm-mediated PMN activation.
- To elucidate which complement pathway is involved in sperm-induced PMN activation.
Main Methods:
- Measurement of chemiluminescence emitted by PMN as an indicator of activation.
- Incubation of PMN with human spermatozoa in the presence of different serum preparations (normal, heat-inactivated, agammaglobulinemic, MgEGTA-treated).
- Assessment of the influence of sperm viability on PMN activation.
Main Results:
- Spermatozoa activated PMN in the presence of serum containing antibodies, complement, or only the alternative complement pathway.
- Activation was dependent on sperm concentration, serum concentration, and the presence of antibody or complement.
- Heat-inactivated agammaglobulinemic serum (lacking both antibodies and complement) did not induce significant PMN activation.
- Dead spermatozoa demonstrated a greater capacity to activate PMN compared to viable spermatozoa.
Conclusions:
- Human spermatozoa activate the alternative pathway of the complement system.
- Spermatozoa-mediated PMN activation is dependent on complement activation.
- Sperm viability influences the extent of PMN activation, suggesting a role for damaged sperm in immune responses.