Gel electrophoresis of human sperm: a simple method for evaluating sperm protein quality |
| |
Authors: | Jumeau Fanny Fernandez-Gomez Francisco-Jose Eddarkaoui Sabiha Duban-Deweer Sophie Buée Luc Béhal Hélène Sergeant Nicolas Mitchell Valérie |
| |
Affiliation: | 1.EA 4308 - GQG – Gametogenesis and gamete quality,University of Lille,Lille,France;2.CHU Lille, Reproductive Biology – Spermiology – CECOS Institute,Lille,France;3.University of Lille, Institut National de la Santé et de la Recherche Medicale (INSERM), CHU Lille,Lille,France;4.EA 2465 - LBHE Blood-Brain Barrier Laboratory,University of Artois,Lens,France;5.CHU Lille, EA 2694 - Santé publique: épidémiologie et qualité des soins,University of Lille,Lille,France;6.Present address: Reproductive Biology Laboratory - CECOS,Rouen University Hospital,Rouen,France |
| |
Abstract: | BackgroundThe limitations of conventional sperm analyses have highlighted the need for additional means of evaluating sperm quality.MethodsIn a study of a cohort of 245 men with known conventional sperm parameters, one-dimensional PAGE was used to monitor protein content and quality in samples from individual ejaculates.ResultsThe sperm protein content varied markedly from sample to another, especially in the high-molecular-weight range. The intensity of the 80–110 kDa bands was correlated with progressive motility (r?=?0.15, p?=?0.015) and was significantly higher (p?=?0.0367) in the group of men with conventional parameters above the World Health Organization’s 2010 reference values than in the group with at least one subnormal parameter (i.e. semen volume, sperm concentration, sperm count per ejaculate, progressive motility, proportion of normal forms or multiple anomaly index below the lower reference value). Using mass spectrometry, the 80–110 kDa bands were found to correspond primarily to three proteins from the flagellum’s fibrous sheath: A-kinase anchor protein 4, A-kinase anchor protein 3, and spermatogenic cell-specific type 1 hexokinase.ConclusionOne-dimensional PAGE constitutes a simple, rapid, reliable, inexpensive method for analyzing proteins associated with sperm motility in individual human ejaculates. |
| |
Keywords: | |
本文献已被 SpringerLink 等数据库收录! |
|