Abstract
Purpose: Our purpose was to determine the most suitable marker for the human sperm acrosome reaction, based on detection of CD46 antibody binding compared with lectin binding.
Methods: Flow cytometric analysis of CD46 antibody versus lectins (PNA, PSA, and Con A) was used to quantify the acrosome reaction of human sperm.
Results: Neither PSA nor Con A was able to detect significant changes in the spontaneous and ionophore-induced acrosome reactions compared to CD46 antibody. However, PNA was found to exhibit a binding pattern similar to that observed with CD46 and could be used to quantify measurable changes in acrosomal response to ionophore, albeit of a lower magnitude than the responses detected by CD46.
Conclusions: We conclude that PNA binds to the inner acrosomal membrane of acrosome-reacted sperm and is suitable for use as a marker of the acrosome reaction by flow cytometry. Data are presented which clarify the assessment of the acrosome reaction when CD46 and lectins are used.
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Carver-Ward, J.A., Moran-Verbeek, I.M. & Hollanders, J.M.G. Comparative flow cytometric analysis of the human sperm acrosome reaction using CD46 antibody and lectins. J Assist Reprod Genet 14, 111–119 (1997). https://doi.org/10.1007/BF02765780
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DOI: https://doi.org/10.1007/BF02765780