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Abstract
We examined the modification of MC31 molecule during
capacitation, the acrosome reaction, and studied its
role in fertilization. These studies revealed that the
molecular mass of MC31 in cauda spermatozoa was
approximately 28,000-26,000 Daltons (28 kDa-26 kDa). A
limited change in molecular mass was seen in capacitated
spermatozoa. Treatment of sperm extracts with
peptide-N-glycosidase (PN glycosidase) reduced the
molecular mass of MC31 in both cauda and capacitated
spermatozoa from 28 kDa-26 kDa to 23 kDa-20 kDa,
suggesting that MC31 from both cauda and capacitated
spermatozoa is glycosylated, and indicating that
capacitation induces minor post-translational
modifications in the structure of the MC31 antigen. The
MC31 antigen was redistributed from the midpiece of cauda
epididymal spermatozoa to the head and equatorial segment
(ES) after capacitation and acrosome reaction,
respectively, when traced by indirect immunofluorescence
under in vitro fertilization (IVF) conditions. Some
spermatozoa did not stain for the MC31 antigen and might
represent spermatozoa that have shed the antigen. IVF
experiments conducted to assess the effect of an anti-MC31
monoclonal antibody (mMC31) revealed that this antibody
significantly (P < 0.01) inhibited fertilization of
cumulus-invested zona pellucida-intact and the zona
pellucida-free oocytes in a dose-dependent manner.
However, sperm-oolemma binding was not affected. These
findings suggest the MC31 antigen facilitates sperm-oocyte
interactions.
Key words:
Male Reproductive Tract
Fertilization
In vitro fertilization
Sperm
Sperm maturation
This article has been cited by other articles:
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M. S. Wakle, S. A. Joshi, and V. V. Khole Monoclonal Antibody From Vasectomized Mouse Identifies a Conserved Testis-Specific Antigen TSA70 J Androl, November 1, 2005; 26(6): 761 - 771. [Abstract] [Full Text] [PDF] |
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