Hyne R V, Garbers D L
Proc Natl Acad Sci U S A. 1979 Nov;76(11):5699-703. doi: 10.1073/pnas.76.11.5699.
Experiments were designed to determine the interrelationship between cyclic AMP and Ca(2+) during the processes of sperm capacitation and the acrosome reaction. In minimal culture media containing pyruvate and lactate as substrates, guinea pig spermatozoa required a minimum of 1.0-1.5 hr to capacitate in the presence of 1.7 mM Ca(2+) and a minimum of 0.5-1.0 hr to capacitate in the absence of added Ca(2+). Sperm cyclic AMP concentrations were increased by as much as 30-fold within 0.5 min after addition of cells to various media containing Ca(2+), and the concentrations then remained increased for up to 4 hr. When the cells were added to several Ca(2+)-deficient media, however, cyclic AMP concentrations increased only about 3-fold within 0.5 min and then returned to basal concentrations within 2 min. D-600, a calcium transport antagonist, completely blocked the Ca(2+)-induced increase in sperm cyclic AMP concentrations. In contrast to capacitation, the acrosome reaction failed to occur in the absence of extracellular Ca(2+). After capacitation of spermatozoa in a Ca(2+)-free medium, addition of Ca(2+) caused an increase in sperm cyclic AMP concentrations within 1 min and a maximal number of spermatozoa showing an acrosome reaction within 10 min. The addition of 1-methyl-3-isobutylxanthine along with Ca(2+) had a synergistic effect on the increase in cyclic AMP. Neither 1-methyl-3-isobutylxanthine nor 8-Br cyclic AMP induced an acrosome reaction in capacitated spermatozoa in the absence of Ca(2+), but both significantly decreased the time required for maximal expression of the acrosome reaction in the presence of Ca(2+). These results suggest that the sperm acrosome reaction is associated with both a primary transport of Ca(2+) and a Ca(2+)-dependent increase in sperm cyclic AMP concentrations. Because a cyclic AMP analogue did not induce an acrosome reaction in the absence of added Ca(2+), the increase in sperm cyclic AMP concentrations induced by Ca(2+) probably reflects one of a number of Ca(2+)-dependent events associated with the acrosome reaction.
实验旨在确定在精子获能和顶体反应过程中环磷酸腺苷(cyclic AMP)与钙离子(Ca(2+))之间的相互关系。在以丙酮酸和乳酸作为底物的最低限度培养基中,豚鼠精子在存在1.7 mM钙离子的情况下,至少需要1.0 - 1.5小时才能获能;在不添加钙离子的情况下,至少需要0.5 - 1.0小时才能获能。将细胞加入含有钙离子的各种培养基后,精子环磷酸腺苷浓度在0.5分钟内可增加多达30倍,然后在长达4小时内一直保持升高状态。然而,当将细胞加入几种缺乏钙离子的培养基中时,环磷酸腺苷浓度在0.5分钟内仅增加约3倍,然后在2分钟内恢复到基础浓度。钙离子转运拮抗剂D - 600完全阻断了钙离子诱导的精子环磷酸腺苷浓度升高。与获能不同,在没有细胞外钙离子的情况下,顶体反应无法发生。在无钙培养基中使精子获能后,加入钙离子会在1分钟内导致精子环磷酸腺苷浓度升高,并在10分钟内使出现顶体反应的精子数量达到最大值。同时加入1 - 甲基 - 3 - 异丁基黄嘌呤(1 - methyl - 3 - isobutylxanthine)和钙离子对环磷酸腺苷的升高有协同作用。在没有钙离子的情况下,1 - 甲基 - 3 - 异丁基黄嘌呤和8 - 溴环磷酸腺苷(8 - Br cyclic AMP)都不会诱导获能精子发生顶体反应,但在有钙离子存在的情况下,两者都显著缩短了顶体反应最大程度表达所需的时间。这些结果表明,精子顶体反应与钙离子的初级转运以及精子环磷酸腺苷浓度的钙离子依赖性升高都有关。由于在没有添加钙离子的情况下,环磷酸腺苷类似物不会诱导顶体反应,所以钙离子诱导的精子环磷酸腺苷浓度升高可能反映了与顶体反应相关的众多钙离子依赖性事件之一。