Control of APN/CD13 and NEP/CD10 on sperm motility

Aminopeptidase N (APN/CD13) and neutral endopeptidase (NEP/CD10) are enzymes present in human sperm cells and involved in regulation of sperm motility of noncapacitated spermatozoa. We investigated the involvement of APN/CD 13 and NEP/CD 10 in motility and in kinematic parameters of human capacitate...

Full description

Saved in:
Bibliographic Details
Published inAsian journal of andrology Vol. 12; no. 6; pp. 899 - 902
Main Authors Subirán, Nerea, Pinto, Francisco M, Agirregoitia, Ekaitz, Candenas, Luz, Irazusta, Jon
Format Journal Article
LanguageEnglish
Published China Medknow Publications & Media Pvt. Ltd 01.11.2010
Nature Publishing Group
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Aminopeptidase N (APN/CD13) and neutral endopeptidase (NEP/CD10) are enzymes present in human sperm cells and involved in regulation of sperm motility of noncapacitated spermatozoa. We investigated the involvement of APN/CD 13 and NEP/CD 10 in motility and in kinematic parameters of human capacitated spermatozoa. Sperm cells isolated by a discontinuous Percoll gradient (40%-80%) followed up by swim-up techniques were incubated with the APN/CD 13 -specific inhibitor, leuhistin (100 μmol L^-1), and the NEP/CD 10-specific inhibitor, thiorphan (1 μmol L^-1). The complete inhibition of both APN/CD 13 and NEP/CD 10 improved sperm motility. Spermatozoa incubated with the APN/CD13-specific inhibitor lenhistin showed asymmetrical trajectories, whereas sperm trajectories were more regular after treatment with the NEP/CD 10-specific inhibitor thiorphan. In conclusion, APN/CD 13 and NEP/CD 10 modulate the motility of capacitated spermatozoa, although each of the enzymes seems to participate in the control of different aspects of sperm motility. Therefore, both inhibitors may be useful for sperm activation at different functional stages of spermatozoa.
Bibliography:S823.34
APN/CD13, human, hypcractivation, kinematic, motility, NEP/CD10, sperm
TP393
31-1795/R
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1008-682X
1745-7262
DOI:10.1038/aja.2010.82