Human Reproduction, Vol 12, 514-522, Copyright © 1997 by Oxford University Press
MA Akhondi, C Chapple and HD Moore
Human epididymal tissue was recovered from 11 patients undergoing
orchidectomy without anti-androgen treatment. Everted epithelial fragments
from the caput and corpus epididymis of six patients were successfully
cultured in a modified RPMI 1640 medium supplemented with HEPES and
androgens for up to 110 days (mean 56 +/- 28) in 5% CO(2) in air at 37
degrees C. Epithelial cells from human oviduct and non- reproductive tract
cells (breast epithelial cells, fibroblasts) were also cultured for
comparison. The proportion of epididymal epithelial cells in primary
cultures assessed by immunofluorescent localization using a cytokeratin
monoclonal antibody was shown to be >70% for the first 6-8 weeks of
culture. Light and electron microscopy indicated that epithelial cells
maintained polarity and some normal morphology during the culture period.
Washed epididymal or ejaculated spermatozoa prepared by a 'swim-up'
procedure were co-incubated (i) directly with epididymal cells in culture
wells, (ii) in 12 mm Millicell inserts within culture wells, thereby
preventing contact of spermatozoa with culture cells; and (iii) in culture
medium alone. A significant proportion of spermatozoa in direct contact
with culture cells or in Millicell inserts were viable after 6 days of
co-incubation (30-45%) and exhibited progressive motility, while all
spermatozoa in medium alone were non-motile by 3 days. Using
computer-assisted sperm analysis it was shown that the progressive motility
of viable spermatozoa decreased gradually for the first 5 days in culture
and then remained constant (approximately 30 microm/s, average path
velocity). After 12 days of co-incubation, 15 +/- 4% of spermatozoa in
direct contact with epithelial cells remained motile; in one experiment, a
few spermatozoa (<1%) were motile at 17 days. Light and electron
microscope observations indicated that prolonged sperm survival was
associated with close apposition of spermatozoa (by equatorial segment) to
the apical membrane of epithelial cells. Oviductal epithelial cells were
also beneficial for sperm survival, but other cell types had no effect.
ARTICLES
Prolonged survival of human spermatozoa when co-incubated with epididymal cell cultures
Department of Obstetrics and Gynaecology, University of Sheffield, UK.
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