The Role of Complement Component C3b and Its Receptors in Sperm-Oocyte Interaction

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 90; no. 21; pp. 10051 - 10055
• Main Authors: Anderson, Deborah J., Abbott, Amy F., Jack, Richard M.
• Format: Journal Article Conference Proceeding
• Language: English
• Published: Washington, DC National Academy of Sciences of the United States of America 01.11.1993; National Acad Sciences; National Academy of Sciences
• Subjects: Adult; Animals; Antibodies; Biological and medical sciences; Biology; Cell membranes; Complement C3b - metabolism; Cricetinae; Enzymes; Female; Fertilization; Fluorescent Antibody Technique; Fundamental and applied biological sciences. Psychology; Gametes; Humans; Ligands; Male; Mammalian reproduction. General aspects; Mesocricetus; Oocytes; Oocytes - cytology; Oocytes - physiology; Ova; Receptors; Receptors, Complement 3b - metabolism; Reproduction; Sperm-Ovum Interactions - physiology; Spermatozoa; Spermatozoa - cytology; Spermatozoa - physiology; Vertebrates: reproduction; Human; Reproduction; Spermatozoa; Complement C3; Membrane cofactor protein; Cell cell interaction; Acrosome reaction; Fecundation; Complement C3b; Mechanism; Oocyte; Biological receptor
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.90.21.10051

Previous studies have shown that human sperm that have undergone the acrosome reaction express a unique tissue-specific variant of the complement component 3 (C3)-binding molecule membrane cofactor protein (MCP, CD46) and that damaged or dead sperm activate the alternative pathway of complement and bind C3 catabolites. In this study we provide evidence that MCP on sperm that have undergone the acrosome reaction specifically binds dimeric C3b and that human sperm acrosomal proteases released during the acrosome reaction directly cleave C3, facilitating its binding to MCP. Furthermore, human and hamster oocytes can activate the alternative pathway of complement and also bind human C3 fragments. Monoclonal antibodies specific for complement receptors type 1 (CD35) and type 3 (CD11b/CD18) bind to the human oocyte plasma membrane, indicating that specific complement-binding molecules may play a role in the attachment of C3 catabolites to oocytes. Subsaturating concentrations of dimeric C3b (0.01-1 μ M) promoted penetration of hamster oocytes by human sperm, whereas saturating doses (>10 μ M) inhibited this process. In addition, antibodies to both MCP and C3 significantly inhibited penetration of hamster oocytes by human sperm. These data provide evidence that regulated gamete-induced generation of C3 fragments and the binding of these fragments by selectively expressed receptors on sperm and oocytes may be an initial step in gamete interaction, leading to membrane fusion and fertilization.