RIKEN BioResouce Center, Tsukuba, Ibaraki, Japan.
PLoS One. 2010 Jun 11;5(6):e11062. doi: 10.1371/journal.pone.0011062.
Intracytoplasmic sperm injection (ICSI) has been widely used to study the mechanisms of mammalian fertilization and to rescue male-factor infertility in humans and animals. However, very few systematic analyses have been conducted to define factors affecting the efficiency of ICSI. In this study, we undertook a large-scale series of ICSI experiments in mice to define the factors that might affect outcomes.
METHODOLOGY/PRINCIPAL FINDINGS: We used a 5 x 3 x 2 factorial design with the following factors: mouse genotype (ICR, C57BL/6, DBA/2, C3H/He, and 129/Sv strains), type of male germ cells (epididymal sperm, elongated or round spermatids), and their freeze-thawing treatment. The efficiencies (parameters) of each developmental step were analyzed by three-way ANOVA (significance level P<0.01). The type of male germ cells affected all the four parameters observed: oocyte survival after injection, cleavage of oocytes, implantation, and birth of offspring. Genotype affected the oocyte survival, cleavage and birth rates, whereas freeze-thawing had no effects on any of the parameters. There were significant genotype/cell type interactions for oocyte survival and cleavage, indicating that they were determined by a combination of strain and germ cell maturity. Multiple comparisons revealed that spermatozoa and elongated spermatids gave better implantation and birth rates than did round spermatids, while spermatozoa and elongated spermatozoa were indistinguishable in their ability to support embryonic development. The best overall efficiency (birth rate per oocytes injected) was obtained with frozen-thawed DBA/2 strain elongated spermatids (23.2+/-4.2%).
CONCLUSIONS/SIGNIFICANCE: The present study provides the first comprehensive information on ICSI using the mouse as a model and will contribute to the efficient use of materials, time, and efforts in biomedical research and clinics involving ICSI.
胞质内单精子注射(ICSI)已被广泛用于研究哺乳动物受精的机制,并用于治疗人类和动物的男性因素不育。然而,很少有系统的分析来定义影响 ICSI 效率的因素。在这项研究中,我们在小鼠中进行了大规模的 ICSI 实验系列,以定义可能影响结果的因素。
方法/主要发现:我们采用了 5 x 3 x 2 析因设计,包括以下因素:小鼠基因型(ICR、C57BL/6、DBA/2、C3H/He 和 129/Sv 品系)、雄性生殖细胞类型(附睾精子、伸长或圆形精子)及其冻融处理。通过三因素方差分析(显著性水平 P<0.01)分析每个发育步骤的效率(参数)。雄性生殖细胞类型影响观察到的四个参数:注射后卵母细胞的存活、卵母细胞的分裂、着床和后代的出生。基因型影响卵母细胞的存活率、分裂率和出生率,而冻融处理对任何参数均无影响。卵母细胞存活率和分裂率存在显著的基因型/细胞类型相互作用,表明它们由品系和生殖细胞成熟度的组合决定。多重比较显示,精子和伸长的精子比圆形精子具有更好的着床和出生率,而精子和伸长的精子在支持胚胎发育的能力上没有区别。使用冷冻解冻的 DBA/2 品系伸长精子获得了最佳的总体效率(每注射卵母细胞的出生率)(23.2+/-4.2%)。
结论/意义:本研究提供了使用小鼠作为模型的 ICSI 的第一份全面信息,将有助于高效利用材料、时间和精力进行涉及 ICSI 的生物医学研究和临床工作。