Fraser L R
Department of Anatomy and Human Biology, King's College London (KQC), Strand, U.K.
J Reprod Fertil. 1987 Sep;81(1):77-89. doi: 10.1530/jrf.0.0810077.
The minimum and maximum extracellular Ca2+ concentrations required to promote capacitation, the acrosome reaction, hyperactivated motility, zona penetration and gamete fusion in the mouse have been established. The traces of free calcium in Ca2+-deficient medium were shown not to enhance capacitation since the inclusion of EGTA to chelate free ions during a 120 min preincubation failed to alter the kinetics of capacitation from those observed in the absence of EGTA; 1 h after addition of 1.80 mM-Ca2+, both suspensions were highly fertile. Complete capacitation, when suspensions were immediately functional upon the addition of 1.80 mM-Ca2+, required the presence of greater than or equal to 90 microM-Ca2. Considerably higher concentrations were required to initiate optimal sperm responses: acrosome reaction, 900 microM; gamete fusion, 900 microM; hyperactivated motility, 1.80 mM; zona penetration, 1.80 mM. None of these changes was effected when Ca2+ was less than 450 microM. The responses to elevated Ca2+ were dependent on the length of incubation, being initially positive and then negative. A short (30 min) exposure to 3.40 mM-Ca2+ (x 2 the standard) accelerated capacitation, as evidenced by significantly increased acrosome loss, precocious expression of hyperactivated motility and enhanced fertilizing ability when Ca2+ was reduced to 1.80 mM. However, extended (120 min) preincubation irreversibly damaged sperm function. In the presence of 7.20 mM-Ca2+ (x 4), fertilizing ability was inhibited at both 30 and 120 min, despite a high incidence of acrosome loss. The primary deleterious effect appeared to be on motility which was judged to be more erratic than in 1.80 mM-Ca2+, possibly due to elevated intracellular Ca2+. Because of the considerable difference in threshold Ca2+ concentrations, it is now possible to dissociate the Ca2+-dependent events of capacitation from those of the acrosome reaction and motility changes.
促进小鼠精子获能、顶体反应、超活化运动、穿过透明带及配子融合所需的细胞外钙离子浓度的最小值和最大值已经确定。钙离子缺乏培养基中的游离钙痕量未显示出能增强获能作用,因为在120分钟预孵育期间加入乙二醇双四乙酸(EGTA)螯合游离离子并未改变获能动力学,其与未加EGTA时观察到的情况相同;加入1.80 mM钙离子1小时后,两种悬浮液的受精能力都很强。当悬浮液在加入1.80 mM钙离子后立即具有功能时,完全获能需要存在大于或等于90微摩尔/升的钙离子。启动最佳精子反应需要相当高的浓度:顶体反应为900微摩尔/升;配子融合为900微摩尔/升;超活化运动为1.80 mM;穿过透明带为1.80 mM。当钙离子浓度低于450微摩尔/升时,这些变化均未发生。对升高的钙离子的反应取决于孵育时间,最初是正向的,然后是负向的。短时间(30分钟)暴露于3.40 mM钙离子(标准浓度的2倍)可加速获能,当钙离子浓度降至1.80 mM时,顶体丢失显著增加、超活化运动过早表达以及受精能力增强均证明了这一点。然而,延长(120分钟)预孵育会不可逆地损害精子功能。在存在7.20 mM钙离子(标准浓度的4倍)的情况下,尽管顶体丢失发生率很高,但在30分钟和120分钟时受精能力均受到抑制。主要的有害作用似乎是对运动的影响,据判断其比在1.80 mM钙离子中更不稳定,这可能是由于细胞内钙离子升高所致。由于阈值钙离子浓度存在相当大的差异,现在有可能将钙离子依赖的获能事件与顶体反应和运动变化的事件区分开来。