Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF ) Freely available
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (6)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Weidinger, S.
Right arrow Articles by Kohn, F.M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Weidinger, S.
Right arrow Articles by Kohn, F.M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol. 18, No. 12, 2519-2524, December 2003
© 2003 European Society of Human Reproduction and Embryology

Mast cell–sperm interaction: evidence for tryptase and proteinase-activated receptors in the regulation of sperm motility

S. Weidinger1,4, A. Mayerhofer2, M.B. Frungieri2, V. Meineke3, J. Ring1 and F.M. Kohn1

1 Department of Dermatology and Allergy, Technical University Munich, Biedersteiner Strasse 29, 80802 Munich, 2 Department of Anatomy, University of Munich, 80802 Munich and 3 Department of Radiobiology, Military Academy Munich, 80937 Munich, Germany

4 To whom correspondence should be addressed. e-mail: weidinger{at}lrz.tum.de

BACKGROUND: The detection of significant levels of tryptase in human seminal plasma and follicular fluid and of tryptase-positive mast cells (MCs) in the wall of human Fallopian tubes lead us to hypothesize that tryptase may exert regulatory actions on human spermatozoa. METHODS AND RESULTS: Immunoelectronmicroscopy revealed proteinase-activated receptor 2 (PAR-2) in the membranes of the acrosomal region and midpiece of human spermatozoa. These PAR-2 were functional, as exposure of spermatozoa from healthy men (n = 12) with regular standard semen parameters to human recombinant tryptase significantly decreased motility in a dose- and time-dependent fashion. Motile spermatozoa (WHO a + b) were significantly decreased within 10 min of incubation with 1.000 ng/ml tryptase (P = 0.045). After 30 and 60 min, significant reduction of motility was also observed in the presence of lower tryptase concentrations (100 ng/ml, P = 0.037; 10 ng/ml, P = 0.046). The inhibitory effects of tryptase progressed throughout an observation period of 180 min. Furthermore, tryptase effects were reversible after washing procedures and could be inhibited by pretreatment with anti-tryptase antibody or anti-PAR-2 antiserum. CONCLUSIONS: The observations presented raise the possibility that tryptase directly interacts with human spermatozoa during their migration through the female genital tract. Genital tract MCs and their products may be as yet unrecognized factors involved in human fertility/sterility.

Key words: motility/PAR-2/spermatozoa/tryptase


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Biol. Reprod.Home page
Y. Radhakrishnan, K. G. Hamil, J.-a. Tan, G. Grossman, P. Petrusz, S. H. Hall, and F. S. French
Novel Partners of SPAG11B Isoform D in the Human Male Reproductive Tract
Biol Reprod, October 1, 2009; 81(4): 647 - 656.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
S. Weidinger, A. Mayerhofer, L. Kunz, M. Albrecht, M. Sbornik, E. Wunn, R. Hollweck, J. Ring, and F.M. Kohn
Tryptase inhibits motility of human spermatozoa mainly by activation of the mitogen-activated protein kinase pathway
Hum. Reprod., February 1, 2005; 20(2): 456 - 461.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.