Oligomycin A-induced inhibition of mitochondrial ATP-synthase activity suppresses boar sperm motility and in vitro capacitation achievement without modifying overall sperm energy levels

Laura Ramió-Lluch, Marc Yeste, Josep M. Fernández-Novell, Efrén Estrada, Luiz Rocha, José A. Cebrián-Pérez, Teresa Muiño-Blanco, Ilona I. Concha, Alfredo Ramírez, Joan E. Rodríguez-Gil

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32 Citations (Scopus)

Abstract

Incubation of boar spermatozoa in a capacitation medium with oligomycin A, a specific inhibitor of the F0 component of the mitochondrial ATP synthase, induced an immediate and almost complete immobilisation of cells. Oligomycin A also inhibited the ability of spermatozoa to achieve feasible in vitro capacitation (IVC), as measured through IVC-compatible changes in motility patterns, tyrosine phosphorylation levels of the acrosomal p32 protein, membrane fluidity and the ability of spermatozoa to achieve subsequent, progesterone-induced in vitro acrosome exocytosis (IVAE). Both inhibitory effects were caused without changes in the rhythm of O<inf>2</inf> consumption, intracellular ATP levels or mitochondrial membrane potential (MMP). IVAE was accompanied by a fast and intense peak in O<inf>2</inf> consumption and ATP levels in control spermatozoa. Oligomycin A also inhibited progesterone-induced IVAE as well as the concomitant peaks of O<inf>2</inf> consumption and ATP levels. The effect of oligomycin on IVAE was also accompanied by concomitant alterations in the IVAE-induced changes on intracellular Ca2+ levels and MMP. Our results suggest that the oligomycin A-sensitive mitochondrial ATP-synthase activity is instrumental in the achievement of an adequate boar sperm motion pattern, IVC and IVAE. However, this effect seems not to be linked to changes in the overall maintenance of adequate energy levels in stages other than IVAE. Journal compilation © CSIRO 2014.
Original languageEnglish
Pages (from-to)883-897
JournalReproduction, Fertility and Development
Volume26
Issue number6
DOIs
Publication statusPublished - 1 Jan 2014

Keywords

  • acrosome exocytosis
  • ATP
  • chemiosmosis
  • consumption

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