Progesterone exerts an extragenomic action on human spermatozoa, inclu
ding a calcium transient in the acrosomal domain of these cells via pu
tative receptor sites located on the sperm surface. The calcium transi
ent can be visualized in >80% of spermatozoa treated with this steroid
although their capacity to respond to the calcium signal is heavily d
ependent on their capacitation status, Capacitation is, in turn, depen
dent on a redox-regulated increase in tyrosine phosphorylation that pr
imes the spermatozoa in such a way that the primary calcium influx ind
uced by progesterone is followed by a chloride efflux and the onset of
secondary calcium oscillations, The way in which these changes precip
itate a biological response and the nature of the molecular pathways o
rchestrating these events are currently unknown.