Lee H C, Johnson C, Epel D
Dev Biol. 1983 Jan;95(1):31-45. doi: 10.1016/0012-1606(83)90004-0.
The changes in the intracellular pH (pHi) of sea urchin sperm associated with motility initiation and acrosome reaction were investigated using uptake of two different probes; 9-aminoacridine and methylamine, as a qualitative index. Sperm suspended in Na+-free sea water were immotile and able to concentrate these amines 20-fold or greater indicating that pHi is more acidic than the external medium (pHo = 7.7). This uptake ratio was essentially constant over a wide range of probe and sperm concentrations. Discharge of the pH gradient with specific ionophores (nigericin, monensin, and tetrachlorosalicylanilide) or nonspecifically using low concentration of detergents (Triton X-100 and lysolecithin) all resulted in the release of the probes indicating they are indeed sensing the pH gradient across the sperm membrane. Addition of Na+ to sperm suspended in Na+-free sea water resulted in activation of motility with concomitant efflux of the probes indicating the alkalinization of pHi by 0.4-0.5 pH units. That this pHi change is the causal trigger of motility was suggested by experiments using NH4Cl and nigericin, which increased the pHi and resulted in activation of motility in the absence of Na+. When sperm were directly diluted into artificial sea water (motility activated), a slow reacidification of pHi was observed in one species of sea urchin (L. pictus) but not in the other (S. purpuratus). This acidification could be blocked by mitochondrial inhibitors, verapamil, or the removal of external calcium suggesting that the increase in metabolic activity stimulated by the influx of Ca2+ is responsible for the reacidification. Induction of acrosome reaction further alkalinized the pHi by about 0.16 pH units and was also followed by prolonged reacidification which correlated with the observed increase in Ca2+ uptake. Either mitochondrial agents or the removal of external Ca2+ could also block this pHi change suggesting a similar mechanism is involved.
利用两种不同的探针(9-氨基吖啶和甲胺)的摄取作为定性指标,研究了与海胆精子运动起始和顶体反应相关的细胞内pH(pHi)变化。悬浮在无钠海水中的精子是不动的,并且能够将这些胺浓缩20倍或更多,这表明pHi比外部介质(pHo = 7.7)更酸。在广泛的探针和精子浓度范围内,这种摄取率基本恒定。用特定离子载体(尼日利亚菌素、莫能菌素和四氯水杨苯胺)或使用低浓度去污剂(曲拉通X-100和溶血卵磷脂)非特异性地消除pH梯度,均导致探针释放,表明它们确实在感知跨精子膜的pH梯度。向悬浮在无钠海水中的精子中添加Na+会导致运动激活,同时探针外流,表明pHi碱化0.4-0.5个pH单位。使用NH4Cl和尼日利亚菌素的实验表明,这种pHi变化是运动的因果触发因素,在没有Na+的情况下,它们会提高pHi并导致运动激活。当精子直接稀释到人工海水中(运动被激活)时,在一种海胆(紫海胆)中观察到pHi缓慢再酸化,但在另一种海胆(花棘海胆)中未观察到。这种酸化可被线粒体抑制剂、维拉帕米或去除外部钙所阻断,这表明由Ca2+内流刺激的代谢活性增加是再酸化的原因。顶体反应的诱导进一步使pHi碱化约0.16个pH单位,随后也出现长时间的再酸化,这与观察到的Ca2+摄取增加相关。线粒体药物或去除外部Ca2+也可以阻断这种pHi变化,表明涉及类似的机制。