Inhibition of forward and reverse transport of Ca2+ via Na+/Ca2+ exchangers (NCX) prevents sperm capacitation
dc.contributor.author
dc.date.accessioned
2024-09-04T09:41:33Z
dc.date.available
2024-09-04T09:41:34Z
dc.date.issued
2024-08-23
dc.identifier.issn
0716-9760
dc.identifier.uri
dc.description.abstract
Background: While calcium is known to play a crucial role in mammalian sperm physiology, how it flows in and out of the male gamete is not completely understood. Herein, we investigated the involvement of Na+/Ca2+ exchangers (NCX) in mammalian sperm capacitation. Using the pig as an animal model, we first confirmed the presence of NCX1 and NCX2 isoforms in the sperm midpiece. Next, we partially or totally blocked Ca2+ outflux (forward transport) via NCX1/NCX2 with different concentrations of SEA0400 (2-[4-[(2,5-difluorophenyl)methoxy]phenoxy]-5-ethoxyaniline; 0, 0.5, 5 and 50 µM) and Ca2+ influx (reverse transport) with SN6 (ethyl 2-[[4-[(4-nitrophenyl)methoxy]phenyl]methyl]-1,3-thiazolidine-4-carboxylate; 0, 0.3, 3 or 30 µM). Sperm were incubated under capacitating conditions for 180 min; after 120 min, progesterone was added to induce the acrosome reaction. At 0, 60, 120, 130, and 180 min, sperm motility, membrane lipid disorder, acrosome integrity, mitochondrial membrane potential (MMP), tyrosine phosphorylation of sperm proteins, and intracellular levels of Ca2+, reactive oxygen species (ROS) and superoxides were evaluated. Results: Partial and complete blockage of Ca2+ outflux and influx via NCX induced a significant reduction of sperm motility after progesterone addition. Early alterations on sperm kinematics were also observed, the effects being more obvious in totally blocked than in partially blocked samples. Decreased sperm motility and kinematics were related to both defective tyrosine phosphorylation and mitochondrial activity, the latter being associated to diminished MMP and ROS levels. As NCX blockage did not affect the lipid disorder of plasma membrane, the impaired acrosome integrity could result from reduced tyrosine phosphorylation. Conclusions: Inhibition of outflux and influx of Ca2+ triggered similar effects, thus indicating that both forward and reverse Ca2+ transport through NCX exchangers are essential for sperm capacitation
dc.description.sponsorship
This research was funded by the Ministry of Science, Innovation and Universities, Spain (Grant: PID2020-113320RB-I00), the Regional Government of Catalonia, Spain (2017-SGR-1229 and 2021-SGR-00900), and the Catalan Institution for Research and Advanced Studies (ICREA)
dc.format.extent
17 p.
dc.format.mimetype
application/pdf
dc.language.iso
eng
dc.publisher
BioMed Central (BMC)
dc.relation
PID2020-113320RB-I00
dc.relation.isformatof
Reproducció digital del document publicat a: https://doi.org/10.1186/s40659-024-00535-9
dc.relation.ispartof
Biological Research, 2024, vol. 57, art.núm. 57, p. 1-17
dc.relation.ispartofseries
Articles publicats (D-B)
dc.rights
Attribution 4.0 International (CC BY 4.0)
dc.rights.uri
dc.source
Yeste Oliveras, Marc Ahmad, Adeel Viñolas Vergés, Estel Recuero, Sandra Bonet, Sergi Pinart Nadal, Elisabeth 2024 Inhibition of forward and reverse transport of Ca2+ via Na+/Ca2+ exchangers (NCX) prevents sperm capacitation Biological Research 57 art.núm. 57 1 17
dc.subject
dc.title
Inhibition of forward and reverse transport of Ca2+ via Na+/Ca2+ exchangers (NCX) prevents sperm capacitation
dc.type
info:eu-repo/semantics/article
dc.rights.accessRights
info:eu-repo/semantics/openAccess
dc.relation.projectID
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-113320RB-I00/ES/IMPLICACION DE LA FUNCION MITOCONDRIAL EN LA LONGEVIDAD DEL ESPERMATOZOIDE DE ESPECIES DE INTERES PRODUCTIVO Y DISEÑO DE DILUYENTES PARA SU CONSERVACION/
dc.type.version
info:eu-repo/semantics/publishedVersion
dc.identifier.doi
dc.identifier.idgrec
039109
dc.contributor.funder
dc.type.peerreviewed
peer-reviewed
dc.relation.FundingProgramme
dc.relation.ProjectAcronym
dc.identifier.eissn
0717-6287
dc.identifier.PMID
39175101
dc.identifier.PMCID
PMC11342557