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Biology of Reproduction, Vol 10, 293-308, Copyright © 1974 by Society for the Study of Reproduction
1 Institute for Molecular and Cellular Evolution, University of Miami,
Coral Gables, Florida 33134 Rabbit sperm were immobilized in 5 min after mixing with antibody (goat antisemen;
antiepididymal sperm) and unheated complement (C'). Heated C' was ineffective. Ultrastructural examination of the immobilized sperm revealed cell membrane damage, namely,
rupture at the acrosomal apex. Otherwise, the trilaminar cell membrane structure was
retained. 10-nm "holes" similar to those reported in lysed erythrocytes were not observed.
Amorphous material coated both antibody and control goat globulin-treated sperm. At
least in the case of the control, this may be related to the natural agglutinins for rabbit
cells present in normal goat serum. Striking changes occurred in the outer acrosomal
membrane (oAcm) of the immobilized sperm. These consisted of regularly spaced 60- to 200-nm holes through which the acrosomal material exuded. In extreme cases, the
sperm cell membrane in the acrosomal region, the oAcm, and the acrosomal material
were all absent exposing the inner acrosomal membrane of the immobilized sperm. Treatment with goat antiseminal plasma (antigen from vasectomized male) globulin plus C
did not produce sperm immobilization or ultrastructural changes. The observations suggest
that sperm immobilization results from antibodycomplement rupture of the sperm cell
membrane and a special reaction in the oAcm of the acrosomal apparatus.
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