Fechter J, Schöneberg A, Schatten G
Department of Zoology, University of Wisconsin, Madison 53706, USA.
Cell Motil Cytoskeleton. 1996;35(4):281-8. doi: 10.1002/(SICI)1097-0169(1996)35:4<281::AID-CM1>3.0.CO;2-A.
To determine the fate of the sperm tail during fertilization, the microtubules of the incorporated axoneme are measured using a monoclonal antibody against acetylated alpha-tubulin in zygotes from the sea urchin Strongylocentrotus purpuratus. This antibody recognizes axonemal microtubules, but does not recognize egg cytoplasmic tubulin or microtubules. The detachment of the axoneme from the male pronucleus occurs as early as 15 min post-insemination. Following excision, the axoneme is often found in close association with the female pronucleus during its migration to the male pronucleus. Fragmentation of the sperm tail, detected at 25 min, continues with only a few micrometers remaining at 85 min post-insemination. The fluorescence intensity of the axonemal fragments diminishes over time as compared to intact axonemes. At 100 min post-insemination, the sperm axoneme is no longer detected. Alternative imaging approaches using brief cold or elevated calcium extraction to disrupt the labile cytoplasmic, but not axonemal, microtubules, indicate that these observations are not due to changes in the post-translational modifications of alpha-tubulin. In the presence of nocodazole, a microtubule assembly inhibitor, a large portion of the tail remains visible at 100 min post-insemination; this suggests that microtubule dynamics are required for the disassembly of the sperm tail. Furthermore, the detachment of the axoneme from the male pronucleus requires the formation of the sperm aster. This suggests that the sperm aster microtubules both detach the axoneme from the male pronucleus, and also cause the translocation of the tail towards the female pronucleus after pronuclear union. In summary, the sperm tail is excised from the male pronucleus and the tail microtubules disassembled during the first cell cycle of sea urchin fertilization, and these events require new microtubule assembly within the zygote.
为了确定受精过程中精子尾部的命运,利用针对海胆紫海胆受精卵中乙酰化α-微管蛋白的单克隆抗体,对并入的轴丝微管进行测量。该抗体可识别轴丝微管,但不能识别卵细胞质微管蛋白或微管。轴丝与雄性原核的分离最早在授精后15分钟发生。切除后,轴丝在向雄性原核迁移过程中常与雌性原核紧密相连。在授精后25分钟检测到精子尾部断裂,到授精后85分钟仅剩下几微米。与完整轴丝相比,轴丝片段的荧光强度随时间减弱。授精后100分钟,不再检测到精子轴丝。使用短暂低温或升高钙离子浓度提取法破坏不稳定的细胞质微管(而非轴丝微管)的其他成像方法表明,这些观察结果并非由于α-微管蛋白翻译后修饰的变化所致。在微管组装抑制剂诺考达唑存在的情况下,授精后100分钟仍有很大一部分尾部可见;这表明微管动力学对于精子尾部的解体是必需的。此外,轴丝与雄性原核的分离需要精子星体的形成。这表明精子星体微管既能使轴丝与雄性原核分离,又能在原核融合后使尾部向雌性原核移动。总之,在海胆受精的第一个细胞周期中,精子尾部从雄性原核上被切除,尾部微管解体,这些过程需要合子内新的微管组装。