Ra. Bronson et Kt. Preissner, MEASUREMENT OF VITRONECTIN CONTENT OF HUMAN SPERMATOZOA AND VITRONECTIN CONCENTRATION WITHIN SEMINAL FLUID, Fertility and sterility, 68(4), 1997, pp. 709-713
Objective: Vitronectin previously has been extracted from human sperma
tozoa and messenger RNA (mRNA) encoding vitronectin localized by rever
se transcriptase in situ polymerase chain reaction (PCR) to spermatocy
tes of human testis. In the present experiments, we have established r
anges for the content of vitronectin in living human spermatozoa and v
itronectin concentration within seminal fluid of human ejaculates. Des
ign: Seminal fluid was obtained by centrifugation and motile sperm sel
ected by swim-up from men with normal and abnormal ejaculates, accordi
ng to World Health Organization criteria, for vitronectin determinatio
ns. Setting: Academic research environment. Main Outcome Measure(s): S
eminal fluid vitronectin concentrations were measured by ELISA and spe
rm vitronectin content by polyacrylamide gel electrophoresis and semiq
uantitative Western blots. Result(s): Vitronectin seminal fluid concen
tration was 1.35 +/- 1.0 mg/mL (mean +/- SD) for normospermic samples
(n = 26) and 0.78 +/- 0.4 mg/mL for azoospermic specimens (n = 6). Vit
ronectin sperm content ranged from 1 to 15 ng/10(6) motile cells (n =
20). Both high-and low-molecular-weight material was observed. Sperm c
ontent of vitronectin did not vary with sperm morphology. Conclusion(s
): These results suggest that spermatozoa represent a major source of
seminal fluid vitronectin, but that a secondary source exists, perhaps
through transudation from serum. (C) 1997 by American Society for Rep
roductive Medicine.