In mammals two meiosis activating sterols (MAS) have been found to activate
meiotic resumption in mouse oocytes, in vitro. FF-MAS (4,4-dimethyl-5 alph
a-cholesta-8,14,24-triene-3 beta-ol) was extracted from human preovulatory
follicular fluid and T-MAS (4,4-dimethyl-5 alpha-cholest-8,24-diene-3 beta-
ol) from bull testicular tissue. Quite unexpected, these two sterols, which
introduce the cholesterol biosynthetic pathway from lanosterol, may be loc
ally acting substances with important physiological function for reproducti
on. FF-MAS and T-MAS are present in the preovulatory follicular fluid of di
fferent mammalian species and have the capacity to initiate resumption of m
eiosis in mouse oocyte cultured in the presence of hypoxanthine, a natural
meiosis maturation inhibitor. FF-MAS is produced by the cumulus cells of in
tact oocyte-cumulus complexes upon FSH-stimulation and provides the oocyte
with a go-signal for the resumption of meiosis. T-MAS constitutes the vast
majority of MAS found in the mammalian testis and in the human ejaculate; i
n particular a high concentration is found in the spermatozoa. T-MAS may be
produced by the spermatids and the presence of T-MAS in spermatozoa may su
ggest that T-MAS plays a role in fertilization by affecting the second meio
tic division. (C) 1999 Wiley-Liss,Inc.