We have previously characterized an 18-19 kDa cationic protein, SOB3, that was detected in the epididymis and localized within the acrosome and on the neck region of human spermatozoa. We suggested that it is involved in secondary sperm binding to the zona pellucida. The present study describes its purification to homogeneity by preparative electrophoresis and non-equilibrium pH gradient electrophoresis. Degenerate primers deduced from microsequencing were used to amplify a specific fragment from human epididymal RNA by reverse transcription-polymerase chain reaction (RT-PCR). This 164 bp fragment was extended by 5' and 3'-RACE to obtain the 548 bp full length cDNA. The open reading frame encodes a 170 amino acid protein. SOB3 is a single copy gene. It is 98% identical to prepro-FALL39 and 100% identical to CAP18, two human genes which were initially identified by screening a human bone marrow (lambda)gt11 library, and which encode an antimicrobial protein. Northern blots of human tissues revealed a 1 kb transcript in corpus and cauda epididymis only, while RT-PCR showed presence of the mRNA in the three epididymal regions and also in round spermatids. The above results suggest that SOB3 has two roles in sperm protection and fertilization, depending on its dual origin and final sperm localization.

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The initiation and propagation of a Ca2+ signal through the egg seems to be the pivotal event in triggering of meiosis resumption. Over the past decade evidence has accumulated suggesting that sperm contact is essential for this phenomenon to occur in most physiological groups. Given their ability to transduce signals, adhesive proteins which are involved in various binding mechanisms such as cell migration, lymphocyte activation, phagocytosis and virus fusion may play a similar role in fertilization. They have been the subject of serious investigation in non-human mammals and some emerging data indicate that they are active in humans as well. Our goal is to review the presence of such molecules on human gametes and their relevant physiological role, i.e., integrins and their ligands, selectins, IgG Fc receptors and leucocyte differentiation markers. We will discuss how they might trigger egg activation through signaling pathways in light of their identified functions in other adhesion systems. The putative participation of specific human sperm proteins will also be evaluated.