| Literature DB >> 22354039 |
Christoph Brenker1, Normann Goodwin, Ingo Weyand, Nachiket D Kashikar, Masahiro Naruse, Miriam Krähling, Astrid Müller, U Benjamin Kaupp, Timo Strünker.
Abstract
The sperm-specific CatSper channel controls the intracellular Ca(2+) concentration ([Ca(2+)](i)) and, thereby, the swimming behaviour of sperm. In humans, CatSper is directly activated by progesterone and prostaglandins-female factors that stimulate Ca(2+) influx. Other factors including neurotransmitters, chemokines, and odorants also affect sperm function by changing [Ca(2+)](i). Several ligands, notably odorants, have been proposed to control Ca(2+) entry and motility via G protein-coupled receptors (GPCRs) and cAMP-signalling pathways. Here, we show that odorants directly activate CatSper without involving GPCRs and cAMP. Moreover, membrane-permeable analogues of cyclic nucleotides that have been frequently used to study cAMP-mediated Ca(2+) signalling also activate CatSper directly via an extracellular site. Thus, CatSper or associated protein(s) harbour promiscuous binding sites that can host various ligands. These results contest current concepts of Ca(2+) signalling by GPCR and cAMP in mammalian sperm: ligands thought to activate metabotropic pathways, in fact, act via a common ionotropic mechanism. We propose that the CatSper channel complex serves as a polymodal sensor for multiple chemical cues that assist sperm during their voyage across the female genital tract.Entities:
Mesh:
Substances:
Year: 2012 PMID: 22354039 PMCID: PMC3321208 DOI: 10.1038/emboj.2012.30
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598