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ADAM3的破坏会损害小鼠精子向输卵管的迁移。

Disruption of ADAM3 impairs the migration of sperm into oviduct in mouse.

作者信息

Yamaguchi Ryo, Muro Yuko, Isotani Ayako, Tokuhiro Keizo, Takumi Kazuhiro, Adham Ibrahim, Ikawa Masahito, Okabe Masaru

机构信息

Research Institute for Microbial Diseases and Pharmaceutical Sciences, Osaka University, Osaka, Japan.

出版信息

Biol Reprod. 2009 Jul;81(1):142-6. doi: 10.1095/biolreprod.108.074021. Epub 2009 Apr 1.

Abstract

Sperm from four different gene-disrupted mouse lines (calmegin [Clgn], Adam1a, Adam2, and Ace) are known to have defective zona-binding ability. Moreover, it is also reported that the sperm from all of these mouse lines exhibit another common phenotype of impaired migration into oviduct despite the large number of sperm found in uterus after coitus. On the other hand, the sperm from the Adam3-disrupted mouse line was reported to have defects in binding ability to zona, but were able to move into the oviduct. In order to clarify the difference, we investigated the migration of ADAM3-null sperm into oviduct precisely by visualizing the sperm by using acrosin-green fluorescent protein as a tag. As a result, in contrast to previous observations, it was demonstrated that the Adam3-disrupted sperm were unable to migrate into the oviduct after coitus. It was ultimately shown that, in five out of five different gene-disrupted mouse lines, the phenotype of impaired sperm binding to zona pellucida was accompanied by the loss of ability of sperm to migrate into the oviduct. This indicates a close relationship between the two phenomena, and also that sperm migration into the oviduct is a crucial step for fertilization.

摘要

已知来自四种不同基因敲除小鼠品系(钙调蛋白[Clgn]、Adam1a、Adam2和Ace)的精子具有缺陷的透明带结合能力。此外,也有报道称,尽管在交配后子宫中发现大量精子,但所有这些小鼠品系的精子都表现出另一种共同的表型,即输卵管迁移受损。另一方面,据报道,来自Adam3基因敲除小鼠品系的精子在与透明带的结合能力上存在缺陷,但能够进入输卵管。为了阐明这种差异,我们通过使用顶体蛋白酶-绿色荧光蛋白作为标记来可视化精子,精确研究了Adam3基因缺失精子向输卵管的迁移。结果,与之前的观察结果相反,证明Adam3基因敲除的精子在交配后无法迁移到输卵管。最终表明,在五种不同的基因敲除小鼠品系中,精子与透明带结合受损的表型伴随着精子进入输卵管能力的丧失。这表明这两种现象之间存在密切关系,也表明精子向输卵管的迁移是受精的关键步骤。

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