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dc.contributor.author
Mata Martínez, Esperanza  
dc.contributor.author
Sánchez Tusie, Ana Alicia  
dc.contributor.author
Darszon, Alberto  
dc.contributor.author
Mayorga, Luis Segundo  
dc.contributor.author
Treviño, Claudia L.  
dc.contributor.author
de Blas, Gerardo Andrés  
dc.date.available
2022-10-20T17:18:57Z  
dc.date.issued
2021-02  
dc.identifier.citation
Mata Martínez, Esperanza; Sánchez Tusie, Ana Alicia; Darszon, Alberto; Mayorga, Luis Segundo; Treviño, Claudia L.; et al.; Epac activation induces an extracellular Ca2+-independent Ca2+ wave that triggers acrosome reaction in human spermatozoa; John Wiley and Sons Inc; Andrology; 9; 4; 2-2021; 1227-1241  
dc.identifier.issn
2047-2919  
dc.identifier.uri
http://hdl.handle.net/11336/174223  
dc.description.abstract
Background: The signaling pathways of the intracellular second messengers cAMP and Ca2+ play a crucial role in numerous physiological processes in human spermatozoa. One such process is the acrosome reaction (AR), which is necessary for spermatozoa to traverse the egg envelope and to expose a fusogenic membrane allowing the egg–sperm fusion. Progesterone and zona pellucida elicit an intracellular Ca2+ increase that is needed for the AR in the mammalian spermatozoa. This increase is mediated by an initial Ca2+ influx but also by a release from intracellular Ca2+ stores. It is known that intracellular Ca2+ stores play a central role in the regulation of [Ca2+]i and in the generation of complex Ca2+ signals such as oscillations and waves. In the human spermatozoa, it has been proposed that the cAMP analog and specific agonist of Epac 8-(p-chlorophenylthio)-2'-O-methyladenosine-3’,5'-cyclic monophosphate (2'-O-Me-cAMP) elicits an intracellular Ca2+ release involved in the AR. Objective: To identify the molecular entities involved in the Ca2+ mobilization triggered by 2'-O-Me-cAMP in human spermatozoa. Materials and Methods: In capacitated human spermatozoa, we monitored Ca2+ dynamics and the occurrence of the AR in real time using Fluo 3-AM and FM4-64 in a Ca2+-free medium. Results: Epac activation by 2'-O-Me-cAMP induced a Ca2+ wave that started in the midpiece and propagated to the acrosome region. This Ca2+ response was sensitive to rotenone, CGP, xestospongin, NED-19, and thapsigargin, suggesting the participation of different ion transporters (mitochondrial complex I and Na+/Ca2+ exchanger, inositol 3-phosphate receptors, two-pore channels and internal store Ca2+-ATPases). Discussion: Our results suggest that Epac activation promotes a dynamic crosstalk between three different intracellular Ca2+ stores: the mitochondria, the redundant nuclear envelope, and the acrosome. Conclusion: The Ca2+ wave triggered by Epac activation is necessary to induce the AR and to enhance the flagellar beat.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
John Wiley and Sons Inc  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
ACROSOME REACTION  
dc.subject
CALCIUM  
dc.subject
EPAC  
dc.subject
FLAGELLAR BEAT  
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INTRACELLULAR CA2+ STORES  
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SPERMATOZOA  
dc.subject.classification
Bioquímica y Biología Molecular  
dc.subject.classification
Ciencias Biológicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Epac activation induces an extracellular Ca2+-independent Ca2+ wave that triggers acrosome reaction in human spermatozoa  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2022-09-22T00:30:17Z  
dc.journal.volume
9  
dc.journal.number
4  
dc.journal.pagination
1227-1241  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Nueva Jersey  
dc.description.fil
Fil: Mata Martínez, Esperanza. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina  
dc.description.fil
Fil: Sánchez Tusie, Ana Alicia. Universidad Autonoma de Queretaro.; México  
dc.description.fil
Fil: Darszon, Alberto. Universidad Nacional Autónoma de México; México  
dc.description.fil
Fil: Mayorga, Luis Segundo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina  
dc.description.fil
Fil: Treviño, Claudia L.. Universidad Nacional Autónoma de México; México  
dc.description.fil
Fil: de Blas, Gerardo Andrés. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina  
dc.journal.title
Andrology  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1111/andr.12989  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/ 10.1111/andr.12989