Membrane cofactor protein (MCP, CD46) in seminal plasma and on spermatozoa in normal and “sterile” subjects

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Abstract
A sperm protein of molecular mass 43 kDa (the spermatozoa membrane cofactor protein, smMCP) and a seminal plasma protein of 60 kDa (ssMCP) were identified by sodium dodecyl sulfate‐polyacrylamide gel electrophoresis (SDS‐PAGE) followed by immunoblotting with four monoclonal antibodies (mAb) against membrane cofactor protein (MCP, CD46).These proteins served as factor I cofactors for the cleavage of methylamine‐treated C3 (C3ma), the activity of which was blocked by M75, an MCP cofactor‐activity‐blocking mAb. Thus, these semen proteins are antigenic and functional homologoues of MCP. On SDS‐PAGE analysis these MCP migrated as single‐band proteins which differed from the two‐band forms of MCP expressed on other cells. smMCP was N‐glycosylated but not O‐glycosylated, while ssMCP was O‐glycosylated: after deglycosylation of these proteins bands were detected at 38‐40 kDa and 43 kDa on SDS‐PAGE, respectively. These semen MCP are therefore, structurally different from the conventional MCP. ssMCP in both normal and “sterile” subject groups was determined by sandwich enzyme‐linked immunosorbent assay. Seminal plasma in the two groups contained 250‐700 ng/ml ssMCP. The difference between the two groups was marginal, although samples from normal subjects tended to show higher concentrations of ssMCP than samples from “sterile” subjects. No molecular difference was observed with ssMCP and smMCP in the two groups by SDS‐PAGE/immunobloblotting analysis. Immunohistochemical analysis suggested that MCP was positive in glandular epithelial cells and the lumen of the prostate, and in most intra‐lumen cells of the testis. Using antibody M177, solubilized prostate and testis were analyzed by immunoblotting and compared with other cell MCP The major band of MCP in the testis, but not in the prostate, was of 60 kDa, which aligned with ssMCP. No band of testis or prostate MCP, however, aligned with smMCP. ssMCP may be produced in the testis, while the origin of smMCP remains unknown. We hypothesize that ssMCP is important in the survival of spermatozoa, protecting them against local secretion of immunoglobulin and complement in the female genital tract, and that smMCP, which is expressed on acrosome‐reacted spermatozoa, plays an essential role in the interaction of spermatozoa with oocytes.