Seminal fluid promotes in vitro sperm-oviduct binding in the domestic cat ([i]Felis catus[/i])

From many endangered or threatened species which are expected to profit from assisted reproduction techniques, mainly epididymal sperm of dead or freshly castrated males are available. These sperm had contact to epididymal secretion products but not to seminal fluid components. Notably, products of accessory sex glands have been shown in domestic animals to condition sperm for fertilization, in particular by mediating sperm-oviduct interaction. We demonstrate for the first time that motile epididymal sperm from domestic cats are able to bind to fresh oviduct epithelial cell explants from preovulatory females [median (min, max) of 10 (8, 16) and 10 (8, 17) sperm per 0.01 mm2 explant surface from both, isthmic and ampullar regions, respectively]. More sperm attach to the explants when epididymal sperm were preincubated for 30 min with seminal fluid separated from electroejaculates of mature tomcats [median (min, max) of 17 (13, 25) and 16 (12, 21) sperm per 0.01 mm2 explant surface from isthmus and ampulla, respectively]. The proportion of bound sperm increased from a median of 54 to 62% by seminal fluid treatment. Sperm-oviduct binding could be facilitated by the decelerated sperm motion which was observed in seminal fluid treated samples, or/and supported by seminal fluid proteins newly attached to the sperm surface. Seminal fluid had no effect on the proportion of sperm with active mitochondria. Extent and pattern of sperm interaction in vitro was independent of explant origin from isthmus or ampulla. Sperm were attached to both, cilia and microvilli of the main epithelial cell types present in all explants. In contrast to published sperm-binding studies with porcine and bovine oviduct explants where predominantly the anterior head region of sperm was attached to ciliated cells, the tails of some cat sperm were firmly stuck to the oviduct cell surfaces while the heads were wobbling. Whether this response is a preliminary step towards phagocytosis or a precondition to capacitation and fertilization remains to be determined. In conclusion, treatment of epididymal sperm with seminal fluid or particular protein components should be considered in future investigations for its potential to improve the outcome of artificial insemination in felids.