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Regular Article |
a MRC Reproductive Biology Unit, Centre for Reproductive Biology, Edinburgh EH3 9EW, United Kingdom
b School of Biological and Chemical Sciences, Centre for Life Sciences, University of Newcastle, Callaghan, NSW 2308, Australia
ABSTRACT
As mammalian spermatozoa migrate through the epididymis, they acquire functionality characterized by the potential to express coordinated movement and the competence to undergo capacitation. The mechanisms by which spermatozoa gain the ability to capacitate during epididymal transit are poorly understood. The purpose of this study was to investigate the impact of epididymal maturation on the signal transduction pathways regulating tyrosine phosphorylation, because this process is thought to be central to the attainment of a capacitated state and expression of hyperactivated motility. Western blot and immunocytochemical analyses demonstrated that epididymal maturation in vivo is associated with a progressive loss of phosphotyrosine residues from the sperm head. As cells pass from the caput to the cauda epididymis, tyrosine phosphorylation becomes confined to a narrow band at the posterior margin of the acrosomal vesicle. Epididymal maturation of rat spermatozoa was also associated with an acquired competence to respond to high levels of intracellular cAMP by phosphorylating tyrosine residues on the sperm tail. Immature caput spermatozoa were incapable of exhibiting this response, despite the apparent availability of cAMP and protein kinase A. These findings help to clarify the biochemical changes associated with the functional maturation of spermatozoa during epididymal transit.
First decision: 3 October 2000.
1 Supported by a grant from GlaxoWellcome Research and Development and the Medical Research Council of the United Kingdom.
2 Correspondence: R. John Aitken, School of Biological and Chemical Sciences, University of Newcastle, Callaghan, NSW 2308, Australia. FAX: 61 2 49 21 6923; jaitken{at}mail.newcastle.edu.au
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