Klemm M, Engel W
Institute for Human Genetics, University of Göttingen, Federal Republic of Germany.
Mol Reprod Dev. 1991 Jan;28(1):47-54. doi: 10.1002/mrd.1080280108.
Acrosome-reacted CB6F1 mouse spermatozoa with slight flagellar motility were microinjected under the zona pellucida of CB6F1 mouse oocytes. Electron microscopy revealed the presence of swollen and decondensed sperm heads in the oocyte cytoplasm. Sixty-one percent of the microinjected oocytes reached a morphologically apparent two-cell stage, but chromosomal analysis demonstrated only haploid chromosomal complements in all cases. The exposure of microinjected oocytes to suspensions of spermatozoa of mice homozygous for a 2,4 reciprocal translocation resulted in normal fertilization and embryonic development with a maternally as well as a paternally derived haploid genome. Identical results were obtained with oocytes microinjected with medium and subjected to in vitro fertilization thereafter. Thus it can be suggested that the microinjected spermatozoa with insufficient flagellar motility are incorporated into the oocyte cytoplasm by phagocytosis. These spermatozoa do not induce a polyspermy block but induce the oocyte to parthenogenetic development.
将鞭毛运动轻微的顶体反应的CB6F1小鼠精子显微注射到CB6F1小鼠卵母细胞的透明带下。电子显微镜显示卵母细胞细胞质中存在肿胀和去浓缩的精子头部。61%的显微注射卵母细胞达到形态上明显的二细胞期,但染色体分析表明所有情况下均只有单倍体染色体组成。将显微注射的卵母细胞暴露于2,4相互易位纯合小鼠精子的悬浮液中,导致正常受精和胚胎发育,具有母源和父源单倍体基因组。用注射培养基后进行体外受精的卵母细胞也得到了相同的结果。因此可以推测,鞭毛运动不足的显微注射精子通过吞噬作用被纳入卵母细胞细胞质中。这些精子不会诱导多精受精阻断,但会诱导卵母细胞进行孤雌生殖发育。