Barnett D K, Kimura J, Bavister B D
Department of Animal Health and Biomedical Sciences, University of Wisconsin-Madison 53706, USA.
Dev Dyn. 1996 Jan;205(1):64-72. doi: 10.1002/(SICI)1097-0177(199601)205:1<64::AID-AJA6>3.0.CO;2-3.
The role of mitochondrial metabolism in the development of preimplantation embryos is unclear. To clarify the importance of mitochondria in early development, the fluorescent probes rhodamine 123 (Rh123: stains active mitochondrial membrane) and nonyl acridine orange (NAO: stains active and inactive mitochondrial membrane) were used with confocal laser scanning microscopy to study the distribution of mitochondria in hamster unfertilized follicular and oviductal eggs (11.5 hr and 16 hr post-hCG, respectively) and preimplantation embryos (1-cell to blastocyst). Rh123 staining indicated that active mitochondria were homogeneously distributed in unfertilized follicular and oviductal eggs. At 3 hr post egg activation (PEA) by sperm, active mitochondria were still found throughout the cytoplasm of the activated egg although they were slightly clustered around the pronuclei and were intensely active in the second polar body. During the next 9 hr, the majority of active mitochondria encircled the apposing pronuclei. By this time the second polar body no longer stained. In 2-cell, 4-cell and 8-cell embryos, there was a striking constancy in the pattern of active mitochondria which were clustered around the nuclei and delineating the cytocortex subjacent to the plasma membrane. In the blastocyst, active mitochondria were most readily detected in the trophectoderm cells in a homogeneous distribution. Staining mitochondria with NAO showed the same distribution patterns as Rh123, indicating that perinuclear clustering of active mitochondria involves the physical movement of these organelles rather than simply changes in their activity. Distribution of actin microfilaments and microtubules showed similar patterns to mitochondria and may be involved in their movement. This migration of mitochondria, beginning during the early stages of fertilization in the hamster egg and persisting until blastocoel formation, must have some functional correlation with successful preimplantation development.
线粒体代谢在植入前胚胎发育中的作用尚不清楚。为了阐明线粒体在早期发育中的重要性,使用荧光探针罗丹明123(Rh123:标记活性线粒体膜)和壬基吖啶橙(NAO:标记活性和非活性线粒体膜),通过共聚焦激光扫描显微镜研究仓鼠未受精卵泡卵和输卵管卵(分别在hCG注射后11.5小时和16小时)以及植入前胚胎(1细胞至囊胚)中线粒体的分布。Rh123染色表明,活性线粒体均匀分布在未受精卵泡卵和输卵管卵中。在精子激活卵子后3小时(PEA),尽管活性线粒体在原核周围略有聚集且在第二极体中高度活跃,但仍可在激活卵子的整个细胞质中发现。在接下来的9小时内,大多数活性线粒体环绕相对的原核。此时第二极体不再染色。在2细胞、4细胞和8细胞胚胎中,活性线粒体的模式具有显著的稳定性,它们聚集在细胞核周围并勾勒出质膜下方的细胞皮质。在囊胚中,活性线粒体最容易在滋养外胚层细胞中以均匀分布被检测到。用NAO对线粒体进行染色显示出与Rh123相同的分布模式,表明活性线粒体的核周聚集涉及这些细胞器的物理移动,而不仅仅是其活性的变化。肌动蛋白微丝和微管的分布显示出与线粒体相似的模式,可能参与了它们的移动。这种线粒体的迁移始于仓鼠卵子受精的早期阶段并持续到囊胚腔形成,必定与成功的植入前发育存在某种功能关联。