Abstract
BackgroundThe in vivo concentration of bicarbonate (HCO3−), one of the essential sperm capacitating effectors, varies greatly in the different environments sperm go through from cauda epididymis to the fertilisation site. On the contrary, porcine in vitro sperm capacitation and fertilisation media usually contains a standard concentration of 25 mmol/L, and one of the main problems presented is the unacceptable high incidence of polyspermy. This work hypothesised that by modifying the HCO3− concentration of the medium, the output of in vitro sperm capacitation and fertilisation could be increased.ResultsOnce exposed to the capacitation medium, the intracellular pH (pHi) of spermatozoa increased immediately even at low concentrations of HCO3−, but only extracellular concentrations of and above 15 mmol/L increased the substrates protein kinase A phosphorylation (pPKAs). Although with a significant delay, 15 mmol/L of HCO3− stimulated sperm linear motility and increased other late events in capacitation such as tyrosine phosphorylation (Tyr-P) to levels similar to those obtained with 25 mmol/L. This information allowed the establishment of a new in vitro fertilisation (IVF) system based on the optimization of HCO3− concentration to 15 mmol/L, which led to a 25.3% increment of the viable zygotes (8.6% in the standard system vs. 33.9%).ConclusionsOptimising HCO3− concentrations allows for establishing an IVF method that significantly reduced porcine polyspermy and increased the production of viable zygotes. A concentration of 15 mmol/L of HCO3− in the medium is sufficient to trigger the in vitro sperm capacitation and increase the fertilisation efficiency in porcine.
Highlights
The in vivo concentration of bicarbonate (HCO3−), one of the essential sperm capacitating effectors, varies greatly in the different environments sperm go through from cauda epididymis to the fertilisation site
The inward transport of HCO3− from the surrounding medium during capacitation involves electrogenic Na+/HCO3− co-transporter (NBC) and Cl−/HCO3− anion exchangers [4]. It starts with induction of the atypical soluble adenylyl cyclase Atypical soluble adenylyl cyclase Adcy10 aka sAC (Adcy10) aka sAC, increase in cAMP
HCO3− is a key factor in inducing sperm capacitation by direct stimulation of Adcy10 before triggering the cascade of fast and slow events of capacitation
Summary
The in vivo concentration of bicarbonate (HCO3−), one of the essential sperm capacitating effectors, varies greatly in the different environments sperm go through from cauda epididymis to the fertilisation site. Once inside the female genital tract, other events occur in a sequential and parallel way for an extended period, such as hyperactivation, tyrosine phosphorylation (Tyr-P) and preparation to undergo acrosome reaction (AR) (slow capacitation events) Both fast and slow events depend on the HCO3− and Ca2+ concentrations, Soriano-Úbeda et al Journal of Animal Science and Biotechnology (2019) 10:19 but the slow ones depend on the presence of cholesterol acceptors like albumin (reviewed by Visconti [3]). The inward transport of HCO3− from the surrounding medium during capacitation involves electrogenic Na+/HCO3− co-transporter (NBC) and Cl−/HCO3− anion exchangers [4] It starts with induction of the atypical soluble adenylyl cyclase Adcy aka sAC ( on Adcy10), increase in cAMP levels and activation of protein kinase A (PKA) [5]
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