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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:

Background

The limitations of conventional sperm analyses have highlighted the need for additional means of evaluating sperm quality.

Methods

In 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.

Results

The 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.

Conclusion

One-dimensional PAGE constitutes a simple, rapid, reliable, inexpensive method for analyzing proteins associated with sperm motility in individual human ejaculates.
Keywords:
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