Rhf. Hunter, Histophysiology of the Fallopian tubes in relation to sperm binding, release, and completion of capacitation, MA MA SY SE, 8, 2001, pp. 279-289
This paper is concerned with endosalpingeal specialisations that underlie s
tabilisation of unique secretions forming microenvironments within the Fall
opian tube lumen, not least as they influence the final stages of sperm tra
nsport and maturation. In particular, a specific microenvironment at the am
pullary-isthmic junction in the presence of the newly-shed oocyte(s), assoc
iated granulosa cells and their secretory products is thought to characteri
se the site of fertilisation. Attention is also drawn to the viscous glycop
rotein in the caudal isthmus before ovulation: it isolates spermatozoa stor
ed with suppressed motility from the metabolic stimulation caused by uterin
e or ampullary fluid. This viscous secretion strips male antigens from the
sperm surface, facilitating their preovulatory binding reactions to organel
les of the isthmus epithelium. Peri-ovulatory activation of discrete number
s of viable spermatozoa is regulated by follicular progesterone secretion,
but seemingly involves local mobilisation of Ca2+ ions into bound gametes o
f appropriate membranous maturity. Motility and progression to the site of
fertilisation may be further heightened by an influence of catecholamines d
iffusing from the myosalpinx; receptors for such molecules are present on t
he sperm surface. There is tight control of sperm activation and release cl
ose to the time of ovulation, generating initial sperm:egg ratios at the am
pullary-isthmic junction of close to unity. However, with establishment of
the block to polyspermy in newly activated eggs and lapse of time after ovu
lation, control of sperm progression soon relaxes. Indeed, 2-4 cell embryos
may contain large numbers of accessory spermatozoa on or in the zona pellu
cida.