Abstract

Sperm storage in the female reproductive tract after mating and before ovulation is a reproductive strategy used by many species. When insemination and ovulation are poorly synchronized, the formation and maintenance of a functional sperm reservoir improves the possibility of fertilization. In mammals, the oviduct regulates sperm functions, such as Ca2+ influx and processes associated with sperm maturation, collectively known as capacitation. A fraction of the stored sperm is released by unknown mechanisms and moves to the site of fertilization. There is an empirical association between the hormonal milieu in the oviduct and sperm detachment; therefore, we tested directly the ability of progesterone to induce sperm release from oviduct cell aggregates. Sperm were allowed to bind to oviduct cells or an immobilized oviduct glycan and then challenged with progesterone, which stimulated the release of 48% of sperm from oviduct cells or 68% of sperm from an immobilized oviduct glycan. The effect of progesterone on sperm release was specific; pregnenolone and 17α-OH-progesterone did not affect sperm release. Ca2+ influx into sperm is associated with capacitation and development of hyperactivated motility. Progesterone increased sperm intracellular Ca2+, which was abrogated by blocking the sperm–specific Ca2+ channel CatSper with NNC 055-0396. NNC 055-0396 also blocked the progesterone-induced sperm release from oviduct cells or immobilized glycan. An inhibitor of the non-genomic progesterone receptor that activates CatSper similarly blocked sperm release. This is the first report indicating that release of sperm from the sperm reservoir is induced by progesterone action through CatSper channels.

Highlights

  • Internal fertilization is part of a reproductive strategy that requires male and female gametes to meet in the female reproductive tract

  • This report documents the importance of progesterone and CatSper channels in the release of porcine sperm from oviduct cells

  • We demonstrated that progesterone stimulates the detachment of porcine sperm from oviduct cell aggregates in vitro through an influx of Ca2+ through CatSper channels

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Summary

Introduction

Internal fertilization is part of a reproductive strategy that requires male and female gametes to meet in the female reproductive tract. One hypothesis is that sperm detachment is due to a change in oviduct fluid components[13] or volume It may be affected by oviduct peristaltic contractions[13] or www.nature.com/scientificreports altered oviduct epithelial cell transcription[14,15]. It has been demonstrated that progesterone stimulates Ca2+ influx in human sperm by binding to a non-genomic receptor, α/β hydrolase domain-containing protein 2 (ABHD2), a serine hydrolase that depletes membrane 2-arachidonylglycerol, releasing inhibition of sperm Ca2+ channels known as CatSper channels[19,20,21,28,29,30]. Functional CatSper channels are necessary for development of human and mouse sperm hyperactivated motility and fertility[22,32,33,34,35]. Because progesterone is involved in CatSper activation in human and macaque sperm[19,20,22,38,39], we explored the function of CatSper channels in progesterone-activated porcine sperm release

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