Kline D, Zagray J A
Department of Biological Sciences, Kent State University, Ohio 44242, USA.
Zygote. 1995 Nov;3(4):305-11. doi: 10.1017/s0967199400002732.
The intracellular pH of the mouse egg was measured during fertilisation to determine whether an increase in pH accompanies activation of this mammalian egg. The pH-sensitive dye BCECF [2',7'-bis-(2-carboxyethyl)-5(and-6)carboxyfluorescein] was introduced into the mouse egg by incubation in BCECF-AM or by microinjection of dextran-conjugated BCECF. The cells were also loaded with the DNA-specific fluorochrome Hoechst 33342 to confirm fertilisation by observation of Hoechst-stained, decondensing sperm heads in the cytoplasm. The ratio of emission intensities for the dye (494/440 nm excitation wavelengths) was monitored continuously with a photon-counting photomultiplier tube. There was no change in pH during or after fertilisation. Control eggs displayed the expected increase in pH when exposed to NH4Cl. In other experiments, intracellular pH and intracellular Ca2+ were monitored simultaneously during fertilisation. The eggs were injected with BCECF dextran and Fura dextran. Fluorescence emission was recorded at excitation wavelengths of 495 nm (BCECF, pH-sensitive wavelength) and 385 nm (Fura, Ca(2+)-sensitive wavelength). A decrease in emission intensity at 385 nm excitation clearly marked the repetitive Ca2+ transients at egg activation. There was no change in the fluorescence emitted at 495 nm excitation, indicating an absence of any change in intracellular pH. These results indicate that intracellular alkalinisation of the cytoplasm does not accompany activation of this vertebrate egg.
在受精过程中对小鼠卵子的细胞内pH值进行了测量,以确定pH值的升高是否伴随这种哺乳动物卵子的激活。通过在BCECF-AM中孵育或显微注射葡聚糖偶联的BCECF,将pH敏感染料BCECF [2',7'-双-(2-羧乙基)-5(和-6)-羧基荧光素]引入小鼠卵子。细胞还用DNA特异性荧光染料Hoechst 33342加载,以通过观察细胞质中Hoechst染色的、解聚的精子头部来确认受精。用光子计数光电倍增管连续监测染料发射强度的比值(激发波长为494/440 nm)。受精期间或受精后pH值没有变化。对照卵子在暴露于NH4Cl时显示出预期的pH值升高。在其他实验中,在受精过程中同时监测细胞内pH值和细胞内Ca2+。向卵子注射BCECF葡聚糖和Fura葡聚糖。在495 nm(BCECF,pH敏感波长)和385 nm(Fura,Ca(2+)敏感波长)的激发波长下记录荧光发射。385 nm激发下发射强度的降低清楚地标志着卵子激活时的重复性Ca2+瞬变。在495 nm激发下发射的荧光没有变化,表明细胞内pH值没有任何变化。这些结果表明,这种脊椎动物卵子的激活不伴随细胞质的细胞内碱化。