The achievement of boar sperm in vitro capacitation is related to an increase of disrupted disulphide bonds and intracellular ROS levels

The aim of this work was to determine the relationship of intracellular reactive oxygen species (ROS) and the disulphide bonds established between sperm proteins with the achievement of capacitation in boar spermatozoa. With this purpose, spermatozoa were incubated in a specifically designed in vitr...

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Detalles Bibliográficos
Autores: Betarelli, Rafael, Rocco, Martina, Yeste Oliveras, Marc|||0000-0002-2209-340X, Fernández Novell, Josep M..|||0000-0002-5349-8303, Placci, Anna, Azevedo Pereira, B., Castillo-Martín, Míriam, Estrada, Efrén|||0000-0002-0824-3651, Peña, Alejandro, Zangeronimo, Marcio Gilberto|||0000-0002-3530-9345, Rodríguez-Gil, Joan E.
Tipo de recurso: artículo
Fecha de publicación:2018
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:catalán
OAI Identifier:oai:ddd.uab.cat:196864
Acceso en línea:https://ddd.uab.cat/record/196864
https://dx.doi.org/urn:doi:10.1111/andr.12514
Access Level:acceso abierto
Palabra clave:Senglars
Acrosome exocytosis
Boar spermatozoa
Free cysteine residues
In vitro capacitation
Reactive oxygen species
Reduced glutathione
Descripción
Sumario:The aim of this work was to determine the relationship of intracellular reactive oxygen species (ROS) and the disulphide bonds established between sperm proteins with the achievement of capacitation in boar spermatozoa. With this purpose, spermatozoa were incubated in a specifically designed in vitro capacitation medium (CM) in the presence or absence of reduced glutathione (GSH). Incubation of boar spermatozoa in CM for 4 h significantly (p < 0.05) increased free cysteine residues, which is a marker of disrupted disulphide bonds, and also intracellular ROS levels. The addition of GSH to the medium prevented most capacitation-like changes in sperm motility, membrane lipid disorder, mitochondrial membrane potential, intracellular calcium levels and localization of tyrosine-phosphorylated proteins (pTyr), but not in tyrosine phosphorylation of P32. These effects were accompanied by the inhibition of the ability of sperm cells to trigger the acrosome exocytosis in response to progesterone. When GSH was added together with progesterone after 4 h of incubation, acrosome exocytosis was not altered, but the subsequent decrease in intracellular calcium observed in controls cells was inhibited. Furthermore, co-incubation of oocytes with spermatozoa previously incubated in CM in the presence of GSH for 4 h significantly (p < 0.05) increased the number of spermatozoa attached to the oocyte surface but decreased normal fertilization rates. Our results suggest that boar sperm capacitation is related to an increase in disrupted disulphide bonds and intracellular ROS levels and that both events are related to the regulation of hyperactivated motility, intracellular calcium dynamics, sperm binding ability to the oocyte and achievement of proper nuclear decondensation upon oocyte penetration.