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Novel epididymal proteins as targets for the development of post-testicular male contraception

Authors :
Matti Poutanen
Jenni Jalkanen
Ilpo Huhtaniemi
Petra Sipilä
Source :
REPRODUCTION. 137:379-389
Publication Year :
2009
Publisher :
Bioscientifica, 2009.

Abstract

Apart from condoms and vasectomy, modern contraceptive methods for men are still not available. Besides hormonal approaches to stop testicular sperm production, the post-meiotic blockage of epididymal sperm maturation carries lots of promise. Microarray and proteomics techniques and libraries of expressed sequence tags, in combination with digital differential display tools and publicly available gene expression databases, are being currently used to identify and characterize novel epididymal proteins as putative targets for male contraception. The data reported indicate that these technologies provide complementary information for the identification of novel highly expressed genes in the epididymis. Deleting the gene of interest by targeted ablation technology in mice or using immunization against the cognate protein are the two preferred methods to functionally validate the function of novel genesin vivo. In this review, we summarize the current knowledge of several epididymal proteins shown eitherin vivoorin vitroto be involved in the epididymal sperm maturation. These proteins include CRISP1, SPAG11e, DEFB126, carbonyl reductase P34H, CD52, and GPR64. In addition, we introduce novel proteinases and protease inhibitor gene families with potentially important roles in regulating the sperm maturation process. Furthermore, potential contraceptive strategies as well as delivery methods will be discussed. Despite the progress made in recent years, further studies are needed to reveal further details in the epididymal sperm maturation process and the factors involved, in order to facilitate the development of new epididymal contraceptives.

Details

ISSN :
17417899 and 14701626
Volume :
137
Database :
OpenAIRE
Journal :
REPRODUCTION
Accession number :
edsair.doi.dedup.....e5d36478040b6958222a488f458255e7