Mn. Llanos et Am. Ronco, SPERM PHOSPHOLIPID METHYLTRANSFERASE ACTIVITY DURING PREPARATION FOR EXOCYTOSIS, Cell biochemistry and function, 12(4), 1994, pp. 289-296
The present report describes experiments to evaluate phospholipid meth
yltransferase activity in golden hamster spermatozoa incubated under d
ifferent conditions. Washed cauda epididymal sperm were incubated with
taurine, in the presence or absence of epinephrine. At various times,
the sperm were separated, and phospholipid methyltransferase activity
measured. Also, at each time, aliquots of the sperm suspension were a
ssayed for motility, and acrosome reactions. Some sperm incubated in t
he presence of taurine and epinephrine were capacitated by 3.5 h, beca
use about 40 per cent of them can undergo the acrosome reaction 10 min
after addition of the fusogen lysophosphatidylcholine. In epinephrine
-free incubations the fusogen failed to stimulate acrosome reactions.
On the other hand, epinephrine stimulated by twofold phospholipid meth
yltransferase activity from '0 time' incubated sperm, in comparison to
that observed in taurine-treated cells. Enzyme activities from both t
aurine or epinephrine plus taurine-treated cells decreased as the incu
bation time of the sperm suspension increased. Kinetic properties of t
he sperm phospholipid methyltransferase activity were modified by the
presence of taurine and epinephrine when S-adenosylmethionine was used
as the substrate. These results suggest that refined molecular events
occur in the sperm cell during the acquisition of fertilizing ability
.