Longo F J, Cook S, McCulloh D H, Ivonnet P I, Chambers E L
Department of Anatomy, University of Iowa, Iowa City 52242, USA.
Zygote. 1994 Nov;2(4):317-31. doi: 10.1017/s0967199400002148.
The site of gamete interaction of electrophysiologically recorded Lytechinus variegatus eggs, fixed with osmium tetroxide (OsO4) and/or glutaraldehyde (GTA) at varying intervals after the onset of the increase in membrane conductance induced by an attached sperm, has been examined by high-voltage and conventional transmission electron microscopy. Although GTA and a GTA-OsO4 mixture induced different electrical responses, specimens prepared with the two fixatives were ultrastructurally similar. In specimens observed within 5 s of the change in conductance, the acrosomal process projected through the vitelline layer and abutted the egg plasma membrane. A conspicuous layer of bindin surrounded the acrosomal process and connected the sperm to the egg's vitelline layer. In a fortuitous specimen fixed within 4 s following the change in conductance, the area of contact between the gamete plasma membranes possessed a trilaminar structure that separated the egg's and sperm's cytoplasms. The morphology of this area of contact was consistent with previously proposed intermediates of membrane fusion. Five to six seconds after the change in conductance, the sperm was connected to the egg via a narrow cytoplasmic bridge that consisted of the former acrosomal process and a projection of the egg cortex. The region of the bridge midway between the fused gametes was encircled by dense material that marked the site of sperm-egg fusion. Gamete interactions in which the activation potential was recorded (unclamped egg) were comparable in time and ultrastructure to events taking place in voltage-clamped eggs except for one major difference. Intact cortical granules (one to three) were observed beneath the tip of the incorporating sperm in unclamped eggs fixed following the onset of the activation potential, whereas all cortical granules dehisced in clamped eggs.
利用高压和传统透射电子显微镜,对在附着精子诱导膜电导增加开始后的不同时间间隔,用四氧化锇(OsO4)和/或戊二醛(GTA)固定的电生理记录的多色刺海胆卵的配子相互作用位点进行了研究。尽管GTA和GTA - OsO4混合物诱导了不同的电反应,但用这两种固定剂制备的标本在超微结构上相似。在电导变化后5秒内观察的标本中,顶体突起穿过卵黄膜并邻接卵质膜。一层明显的结合素围绕着顶体突起,并将精子与卵的卵黄膜连接起来。在电导变化后4秒内固定的一个偶然标本中,配子质膜之间的接触区域具有三层结构,将卵和精子的细胞质分隔开。这个接触区域的形态与先前提出的膜融合中间体一致。电导变化后五到六秒,精子通过一个狭窄的细胞质桥与卵相连,该桥由先前的顶体突起和卵皮质的一个突起组成。融合配子之间桥的中间区域被致密物质环绕,该致密物质标记了精卵融合的位点。记录了激活电位的配子相互作用(未钳制卵)在时间和超微结构上与电压钳制卵中发生的事件相当,但有一个主要区别。在激活电位开始后固定的未钳制卵中,在进入的精子尖端下方观察到完整的皮质颗粒(一到三个),而在钳制卵中所有皮质颗粒都已破裂。