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缺乏CD81的雌性小鼠生育力降低。

Reduced fertility of female mice lacking CD81.

作者信息

Rubinstein Eric, Ziyyat Ahmed, Prenant Michel, Wrobel Edyta, Wolf Jean-Philippe, Levy Shoshana, Le Naour François, Boucheix Claude

机构信息

Inserm U602, Villejuif, France.

出版信息

Dev Biol. 2006 Feb 15;290(2):351-8. doi: 10.1016/j.ydbio.2005.11.031. Epub 2005 Dec 27.

Abstract

In somatic cells, the tetraspanins CD81 and CD9 associate with each other, with additional tetraspanins and with non-tetraspanin molecules to form proteolipidic complexes. Here we show that CD81 is expressed on the surface of oocytes where it associates with tetraspanin-enriched membrane structures. A major CD9 and CD81 partner, CD9P-1, is also expressed by oocytes. Deletion of CD81 gene in mice results in a 40% reduction of female fertility. In vitro insemination indicated that this infertility is due to a deficiency of oocytes to fuse with sperm. While the fertility of CD9-/- mice is severely but not completely impaired, double knock-out CD9-/- CD81-/- mice were completely infertile indicating that CD9 and CD81 play complementary roles in sperm-egg fusion. Finally, a fraction of CD9 was transferred from CD81-/- oocytes to sperm present in the perivitelline space indicating that the defect of fusion of CD81-/- oocytes does not result from an impaired initial gamete interaction.

摘要

在体细胞中,四跨膜蛋白CD81和CD9相互结合,与其他四跨膜蛋白以及非四跨膜蛋白分子形成蛋白脂质复合物。我们在此表明,CD81在卵母细胞表面表达,在该处它与富含四跨膜蛋白的膜结构相关联。卵母细胞还表达一种主要的CD9和CD81结合蛋白CD9P-1。小鼠中CD81基因的缺失导致雌性生育力降低40%。体外受精表明,这种不育是由于卵母细胞与精子融合存在缺陷。虽然CD9基因敲除小鼠的生育力严重受损但未完全丧失,但双基因敲除的CD9-/- CD81-/-小鼠则完全不育,这表明CD9和CD81在精卵融合中发挥互补作用。最后,一部分CD9从CD81基因敲除的卵母细胞转移到卵周隙中的精子上,这表明CD81基因敲除的卵母细胞的融合缺陷并非源于初始配子相互作用受损。

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