Gould-Somero M, Jaffe L A, Holland L Z
J Cell Biol. 1979 Aug;82(2):426-40. doi: 10.1083/jcb.82.2.426.
Previous work has established that the polyspermy block in Urechis acts at the level of sperm-egg membrane fusion. (J. Exp. Zool. 196:105). Present results indicate that during the first 5--10 min after insemination the block is mediated by a positive shift in membrane potential (the fertilization potential) elicited by the penetrating sperm, since holding the membrane potential of the unfertilized egg positive by passing current reduces the probability of sperm entry, while progressively reducing the amplitude of the fertilization potential by decreasing external Na+ progressively enhances multiple sperm penetrations. Also, a normal fertilization potential is correlated with a polyspermy block even under conditions (pH 7) in which eggs do not develop. We have investigated the mechanism of the electrical polyspermy block by quantifying the relationship between sperm incorporation, membrane potential and ion fluxes. Results indicate that the polyspermy block is mediated by the electrial change per se and not by the associated fluxes of Na+, Ca++, and H+.
先前的研究已经证实,刺螠中的多精受精阻断作用于精卵膜融合水平(《实验动物学杂志》196:105)。目前的研究结果表明,在授精后的最初5 - 10分钟内,这种阻断是由穿透的精子引发的膜电位正向变化(受精电位)介导的,因为通过电流使未受精卵的膜电位保持正值会降低精子进入的概率,而通过降低细胞外钠离子浓度逐渐减小受精电位的幅度则会逐渐增加多精穿透的概率。此外,即使在卵子不发育的条件下(pH 7),正常的受精电位也与多精受精阻断相关。我们通过量化精子摄入、膜电位和离子通量之间的关系,研究了电多精受精阻断的机制。结果表明,多精受精阻断是由电变化本身介导的,而不是由相关的钠离子、钙离子和氢离子通量介导的。