Uterosome-like vesicles prompt human sperm fertilizing capability

FRANCHI, A.; BRAVO, A.A.; GUIDOBALDI, H.A.; CUBILLA, M.A.; GIOJALAS, L.C.

MOLECULAR HUMAN REPRODUCTION.

OXFORD UNIV PRESS

Lugar: Oxford; Año: 2016 vol. 22 p. 833 - 841

1360-9947

STUDY QUESTION: Does the rapid transit through the uterine environment modulate the sperm physiological state?SUMMARY ANSWER: The uterosome-like vesicles (ULVs) secreted by endometrial epithelial cells (EECs) in vitro are able to fuse withhuman spermatozoa, prompting their fertilizing capacity.WHAT IS KNOWN ALREADY: Early studies suggest that sperm capacitation begins in the uterus and ends in the oviduct, and that a synergisticeffect of both female organs may accelerate this process. Although it has been reported that co-incubation of human spermatozoawith endometrial cell-conditioned medium (CM) stimulates sperm capacitation, the mechanism mediating this communication is unknown.STUDY DESIGN, SIZE, DURATION: Human ULVs secreted by EECs were characterized and their effect on human sperm physiologywas analysed. Spermatozoa were incubated with EEC-derived CM or ULV, after which sperm capacitation was evaluated at different timepoints. In addition, the interaction of spermatozoa with ULV was analysed.PARTICIPANTS/MATERIALS, SETTING, METHODS: ULVs were isolated by ultracentrifugation and identified using electronmicroscopy and Western blotting to assess the presence of specific protein markers. Following seminal plasma removal, human spermatozoawere incubated CM or ULV, after which sperm capacitation was evaluated as the ability of the sperm to undergo the induced acrosome reactionand the level of protein tyrosine phosphorylation (PY) determined by Western blot and immunocytochemistry. The interaction ofspermatozoa with labelled ULV was analysed by fluorescence microscopy. In all cases, at least three biological replicates from different spermdonors were performed for each set of experiments. Significant differences between mean values were determined by one-way ANOVA followedby Tukey?s post hoc test. Differences between treatments were considered statistically significant at P ¢¢çÜ 0.05.MAIN RESULTS AND THE ROLE OF CHANCE: The level of capacitated spermatozoa and those recruited by chemotaxis increased3- to 4-fold when spermatozoa were incubated in the presence of CM for 4 h. Even a 15 min incubation of spermatozoa with CM was alsoenough to increase the level of capacitated cells 3- to 4-fold (P < 0.05). Furthermore, a short co-incubation of spermatozoa with ULV stimulatessperm capacitation, as determined by the increase in the level of induced acrosome reaction and the induction of PY. In addition, afterthe co-incubation of spermatozoa with fluorescent labelled ULV, the sperm cells acquired the fluorescent staining which indicates that ULVmight be transferred to the sperm surface by a fusion mechanism.LIMITATIONS, REASONS FOR CAUTION: This is an in vitro study performed with human biological material, spermatozoa and endometrialderived cells; the latter being a cell line originally isolated from a uterine adenocarcinoma.WIDER IMPLICATIONS OF THE FINDINGS: The capability of spermatozoa to briefly interact with ULVs supports the hypothesis thatany step of sperm transport may have physiological consequences, despite the interaction lasting for only a limited period of time. This way ofcommunication of spermatozoa with cell products of uterine origin opens new frontiers of investigation (e.g. the signalling moleculesinvolved), shedding light on the sperm processes that prepare the male gamete for fertilization, which might have implications for human infertilitytreatment.LARGE SCALE DATA: N/A.STUDY FUNDING AND COMPETING INTEREST(S): The project was financially supported by SECyT-UNC. The authors declare noconflict of interest.