Antigenic determinants of human sperm tail fibrous sheath proteins

Abstract

Mouse anti-fibrous sheath antisera (MAFA) produced by immunizing mice with purified preparations of human sperm tail fibrous sheath (FS) reacted with the principal piece of less than 10% of freshly isolated spermatozoa which were immotile and probably dead. Following their demembranation by detergents or repeated freezing and thawing, all spermatozoa were stained. This was also demonstrated on spermatozoa dried onto slides, but the undiluted xenoantisera showed additional reactivity with the acrosomal zone (AZ). Using immunogold electron microscopy, the target antigens were ultrastructurally localized to the FS, and a few spermatozoa showed some reaction at the AZ subacrosomal perinuclear theca. Following titration of the antibodies, the anti-AZ-reaction became undetectable at a dilution of 1:20 while their reactivity with the principal piece continued to a 1:400-dilution. These results indicated that the xenoantisera probably contained an additional unrelated antibody component which reacted with the AZ. Western blotting and staining of purified FS with MAFA detected seven major protein bands with MW ranging between 25 kDa and 97.4 kDa. In human testes, the 1:50 diluted MAFA reacted with sperm tails only, indicating the late expression of the antigenic determinants during spermatogenesis. MAFA did not react with oesophagus, stomach, duodenum, ileum, nasal lining tissues, uterus, pericardium, pancreas, thyroid gland, or cultured fibroblasts. The xenoantisera did, however stain the skin epidermis and cultured keratinocytes which exhibited filamentous cytoplasmic staining although their target antigens could not be biochemically identified. These results indicate that the FS proteins express antigenic determinants which are not shared with other cytoskeletal elements within the sperm flagellum or a variety of somatic tissues.