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Post-meiotic gene products as targets for male contraception

Richard Ivell*, Sandra Danner, Martin Fritsch

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

Post-meiotic stages of male germ cell maturation represent an interesting target system for the development of novel male contraceptive agents. In the human, these stages represent a period of only about 16 days differentiation, and thus targeting these cells would represent a contraceptive approach with a relatively rapid onset and equivalent recovery. Results from the Human Genome Project suggest that these cells also express a high number of very specific transcripts, though whether all of these are functional and/or essential for sperm differentiation and function requires more research. Until recently, however, these haploid stages were relatively inaccessible to molecular research because of the lack of appropriate model systems and methods. This situation has recently improved, with several new techniques involving manipulation of primary cells and seminiferous tubules, germ cell transplantation and the development of new immortalized cell-lines. Also, new biochemical approaches are yielding more information about haploid-specific transcription factors, such as GCNF. It is therefore to be expected that soon several new targets for a potential post-meiotic male contraceptive will become available for pharmaceutical development.

OriginalspracheEnglisch
ZeitschriftMolecular and Cellular Endocrinology
Jahrgang216
Ausgabenummer1
Seiten (von - bis)65-74
Seitenumfang10
ISSN0303-7207
DOIs
PublikationsstatusVeröffentlicht - 15.03.2004

Fördermittel

We should like to thank the AMPPA Consortium for their generous support of part of this project, as well as the Deutsche Forschungsgemeinschaft (grants Iv7/10-1 and Iv7/11-1). We are also grateful to Ms. Marga Balvers for help with the morphological techniques. Some aspects of the work represent a part of the PhD thesis of SD in the Faculty of Biology at the University of Hamburg.

TrägerTrägernummer
AMPPA Consortium
Deutsche ForschungsgemeinschaftIv7/10-1, Iv7/11-1

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