首页> 美国卫生研究院文献>Frontiers in Physiology >Aminopurvalanol A a Potent Selective and Cell Permeable Inhibitor of Cyclins/Cdk Complexes Causes the Reduction of in Vitro Fertilizing Ability of Boar Spermatozoa by Negatively Affecting the Capacitation-Dependent Actin Polymerization
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Aminopurvalanol A a Potent Selective and Cell Permeable Inhibitor of Cyclins/Cdk Complexes Causes the Reduction of in Vitro Fertilizing Ability of Boar Spermatozoa by Negatively Affecting the Capacitation-Dependent Actin Polymerization

机译:氨基嘌呤醇A是强效的选择性的和细胞渗透性的细胞周期蛋白/ Cdk复合物抑制剂通过负面影响与获能有关的肌动蛋白聚合反应导致公猪精子的体外受精能力降低。

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摘要

The adoption of high-througput technologies demonstrated that in mature spermatozoa are present proteins that are thought to be not present or active in sperm cells, such as those involved in control of cell cycle. Here, by using an in silico approach based on the application of networks theory, we found that Cyclins/Cdk complexes could play a central role in signal transduction active during capacitation. Then, we tested this hypothesis in the vitro model. With this approach, spermatozoa were incubated under capacitating conditions in control conditions (CTRL) or in the presence of Aminopurvalanol A a potent, selective and cell permeable inhibitor of Cyclins/Cdk complexes at different concentrations (2, 10, and 20 μM). We found that this treatment caused dose-dependent inhibition of sperm fertilizing ability. We attribute this event to the loss of acrosome integrity due to the inhibition of physiological capacitation-dependent actin polymerization, rather than to a detrimental effect on membrane lipid remodeling or on other signaling pathways such as tubulin reorganization or MAPKs activation. In our opinion, these data could revamp the knowledge on biochemistry of sperm capacitation and could suggest new perspectives in studying male infertility.
机译:高通量技术的采用表明,在成熟的精子中存在的蛋白质被认为在精子细胞中不存在或没有活性,例如参与细胞周期控制的蛋白质。在这里,通过使用基于网络理论的计算机模拟方法,我们发现Cyclins / Cdk复合物在获能过程中的信号转导活性中起着核心作用。然后,我们在体外模型中检验了该假设。通过这种方法,将精子在增容条件下,在对照条件下(CTRL)或在氨基紫精醇A的存在下孵育,氨基紫精醇A是一种有效,选择性且细胞可渗透的Cyclins / Cdk复合物抑制剂,浓度不同(2、10和20μM)。我们发现这种治疗引起精子受精能力的剂量依赖性抑制。我们将此事件归因于由于抑制生理捕获依赖的肌动蛋白聚合导致的顶体完整性的丧失,而不是由于对膜脂质重塑或对其他信号途径(如微管蛋白重组或MAPKs活化)的有害影响。我们认为,这些数据可能会改变精子获能的生物化学知识,并可能为研究男性不育症提供新的观点。

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