Volume 9, Issue 5 (September 2007) 9, 690–696; 10.1111/j.1745-7262.2007.00289.x
Protease activated receptor 2 and epidermal growth factor receptor are involved in the regulation of human sperm motility
Karina Zitta, Martin Albrecht, Stephan Weidinger, Artur Mayerhofer and Frank Köhn
1.Department of Dermatology and Allergy, Technical University Munich, Biedersteiner Strasse 29, Munich 80802, Germany 2.Institute of Anatomy, Ludwig-Maximilians-University, Biedersteiner Strasse 29, Munich 80802, Germany
Correspondence: Dr Karina Zitta, Ludwig-Maximilians-University Munich, Institute for Molecular Animal Breeding, Moorversuchsgut, Hackerstrasse 27, 85764 Oberschleiheim, Germany. Fax: +49-89-2180-78402. E-mail: K.Zitta@gen.vetmed.uni-muenchen.de
Received 13 October 2006; Accepted 4 April 2007.
Abstract |
Aim: To investigate mechanisms of tryptase-induced reduction of sperm motility and explore whether epidermal growth factor receptor (EGF-R) and protease activated receptor 2 (PAR-2)- associated pathways are involved.
Methods: Fresh semen was collected from healthy donors (n = 15). Semen parameters and quality were assessed in accordance with the World Health Organization (WHO) criteria. Swim-up sperm were fixed and subjected to immunocytochemistry and immunoelectronmicroscopy with specific antibodies directed against PAR-2 and EGF-R. Protein extractions from swim-up spermatozoa were analyzed by Western blotting with antibodies for both receptors. Motility of spermatozoa was evaluated by computer-assisted semen analysis.
Results: Immunocytochemistry found PAR-2 and EGF-R in approximately 30% of examined human ejaculated spermatozoa. Both receptors were localized in the plasma membrane. Like tryptase, the PAR-2 synthetic agonist SLIGKV reduced sperm motility, and this effect was inhibited by application of two specific EGF-R pathway blockers (AG1478 and PD168393).
Conclusion: The observed reduction of sperm motility by tryptase through the PAR-2 receptor involves EGF-R pathways.
Keywords: spermatozoa, motility, epidermal growth factor receptor, protease activated receptor
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