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Artículo

Epac activation induces an extracellular Ca2+-independent Ca2+ wave that triggers acrosome reaction in human spermatozoa

Mata Martínez, EsperanzaIcon ; Sánchez Tusie, Ana Alicia; Darszon, Alberto; Mayorga, Luis SegundoIcon ; Treviño, Claudia L.; de Blas, Gerardo AndrésIcon
Fecha de publicación: 02/2021
Editorial: John Wiley and Sons Inc
Revista: Andrology
ISSN: 2047-2919
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Bioquímica y Biología Molecular

Resumen

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.
Palabras clave: ACROSOME REACTION , CALCIUM , EPAC , FLAGELLAR BEAT , INTRACELLULAR CA2+ STORES , SPERMATOZOA
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info:eu-repo/semantics/restrictedAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
Identificadores
URI: http://hdl.handle.net/11336/174223
URL: https://onlinelibrary.wiley.com/doi/10.1111/andr.12989
DOI: http://dx.doi.org/ 10.1111/andr.12989
Colecciones
Articulos(IHEM)
Articulos de INST. HISTOLOGIA Y EMBRIOLOGIA DE MEND DR.M.BURGOS
Citación
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
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