首页> 美国卫生研究院文献>Molecular Human Reproduction >Multivariate analysis of male reproductive function in Inpp5b−/− mice reveals heterogeneity in defects in fertility sperm–egg membrane interaction and proteolytic cleavage of sperm ADAMs
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Multivariate analysis of male reproductive function in Inpp5b−/− mice reveals heterogeneity in defects in fertility sperm–egg membrane interaction and proteolytic cleavage of sperm ADAMs

机译:对Inpp5b-/-小鼠雄性生殖功能的多变量分析显示生育能力精子-卵膜相互作用和精子ADAMs的蛋白水解裂解缺陷存在异质性

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摘要

Past work indicated that sperm from mice deficient in the inositol polyphosphate 5-phosphatase Inpp5b have reduced ability to fertilize eggs in vitro and reduced epididymal proteolytic processing of the sperm protein A Disintegrin and A Metalloprotease 2 (ADAM2). On the basis of these data, our central working hypothesis was that reduced ADAM cleavage would correlate with reduced sperm–egg binding and fusion and in turn with reduced male fertility in Inpp5b−/− mice. Multiple endpoints of reproductive functions [mating trials, in vitro fertilization (IVF) assays and ADAM2 and ADAM3 cleavage] were investigated on a male-by-male basis, with pair-wise correlation analysis used to assess the relationships between these various parameters. Motile sperm from Inpp5b−/− mice showed significantly reduced fertilization of zona pellucida-free eggs due to reduced binding to the egg plasma membrane and subsequent fusion. Localization of a mouse sperm protein required for gamete fusion, IZUMO1, appears normal in Inpp5b-null sperm. To our surprise and differing from previous reports, we found that ADAM cleavage was only modestly impaired in numerous Inpp5b-null males and varied between individual animals. Performance in mating trials also differed from past reports. The pair-wise correlation analysis revealed that ADAM2 and ADAM3 cleavage was positively correlated, suggesting that processing of these proteins occurs by related/identical mechanisms, but otherwise, there were few correlations between the reproductive endpoints examined here. Nevertheless, this work provides detailed analysis of the Inpp5b−/− phenotype and also a blueprint for multivariate analysis to examine relationships between molecular characteristics and in vitro and in vivo physiological functions.
机译:过去的工作表明,缺乏肌醇多磷酸5-磷酸酶Inpp5b的小鼠的精子具有降低体外受精卵的能力,并减少了精子蛋白A Disintegrin和A金属蛋白酶2(ADAM2)的附睾蛋白水解过程。根据这些数据,我们的主要工作假说是,ADAM裂解减少会与精子-蛋结合和融合减少有关,进而与Inpp5b -/-小鼠的雄性育性降低有关。生殖功能的多个终点[交配试验,体外受精(IVF)测定以及ADAM2和ADAM3裂解]在男性与男性之间进行了研究,并采用成对相关分析来评估这些不同参数之间的关系。 Inpp5b -/-小鼠的运动精子由于与卵质膜的结合减少和随后的融合而显示出无透明带透明带卵的受精能力显着降低。配子融合所需的小鼠精子蛋白IZUMO1的定位在Inpp5b-null精子中看来是正常的。令我们惊讶的是,与以前的报道不同,我们发现ADAM的裂解仅在无数Inpp5b无效的雄性中受到中等程度的损害,并且在各个动物之间有所不同。交配试验的表现也不同于以往的报告。双向相关分析显示ADAM2和ADAM3裂解呈正相关,表明这些蛋白的加工是通过相关/相同的机制进行的,但除此之外,此处检测的生殖终点之间几乎没有相关性。然而,这项工作提供了Inpp5b -/-表型的详细分析,并且提供了用于进行多变量分析以检查分子特征与体内和体外生理功能之间关系的蓝图。

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