| Literature DB >> 26987518 |
Ida Björkgren1, Luis Alvarez2, Nelli Blank3, Melanie Balbach3, Heikki Turunen1, Teemu Daniel Laajala4, Jussi Toivanen5, Anton Krutskikh6, Niklas Wahlberg7, Ilpo Huhtaniemi6, Matti Poutanen8, Dagmar Wachten3, Petra Sipilä9.
Abstract
During epididymal maturation, sperm acquire the ability to swim progressively by interacting with proteins secreted by the epididymal epithelium. Beta-defensin proteins, expressed in the epididymis, continue to regulate sperm motility during capacitation and hyperactivation in the female reproductive tract. We characterized the mouse beta-defensin 41 (DEFB41), by generating a mouse model with iCre recombinase inserted into the first exon of the gene. The homozygous Defb41(iCre/iCre) knock-in mice lacked Defb41 expression and displayed iCre recombinase activity in the principal cells of the proximal epididymis. Heterozygous Defb41(iCre/+) mice can be used to generate epididymis specific conditional knock-out mouse models. Homozygous Defb41(iCre/iCre) sperm displayed a defect in sperm motility with the flagella primarily bending in the pro-hook conformation while capacitated wild-type sperm more often displayed the anti-hook conformation. This led to a reduced straight line motility of Defb41(iCre/iCre) sperm and weaker binding to the oocyte. Thus, DEFB41 is required for proper sperm maturation.Entities:
Keywords: Beta-defensin; Epididymis; Flagellar motility pattern; Sperm maturation; Sperm-oocyte binding; iCre knock-in
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Year: 2016 PMID: 26987518 DOI: 10.1016/j.mce.2016.03.013
Source DB: PubMed Journal: Mol Cell Endocrinol ISSN: 0303-7207 Impact factor: 4.102