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

被引:6
|
作者
Mata-Martinez, Esperanza [1 ]
Sanchez-Tusie, Ana Alicia [2 ]
Darszon, Alberto [3 ]
Mayorga, Luis S. [1 ,4 ]
Trevino, Claudia L. [3 ]
De Blas, Gerardo A. [1 ,5 ]
机构
[1] Univ Nacl Cuyo, CONICET, Inst Histol & Embriol Dr Mario H Burgos IHEM, Lab Fus Membranas & Exocitosis Acrosomal, Mendoza, Argentina
[2] Univ Autonoma Queretaro, Fac Med, Dept Invest Biomed, Lab Fisiol Celular & Mol, Mexico City, DF, Mexico
[3] Univ Nacl Autonoma Mexico, Inst Biotecnol, Morelos, Mexico
[4] Univ Nacl Cuyo, Fac Ciencias Exactas & Nat, Mendoza, Argentina
[5] Univ Nacl Cuyo, Fac Ciencias Med, Lab Teleanalisis & Invest Traslac, Area Farmacol, Mendoza, Argentina
关键词
acrosome reaction; calcium; Epac; flagellar beat; intracellular Ca2+ stores; spermatozoa; CALCIUM;
D O I
10.1111/andr.12989
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
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.
引用
收藏
页码:1227 / 1241
页数:15
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