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Fyn激酶活性对于小鼠卵母细胞皮质的正常组织和功能极性是必需的。

Fyn kinase activity is required for normal organization and functional polarity of the mouse oocyte cortex.

作者信息

Luo Jinping, McGinnis Lynda K, Kinsey William H

机构信息

Center for Reproductive Sciences, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.

出版信息

Mol Reprod Dev. 2009 Sep;76(9):819-31. doi: 10.1002/mrd.21034.

Abstract

The objective of the present study was to determine whether Fyn kinase participated in signaling events during sperm-egg interactions, sperm incorporation, and meiosis II. The functional requirement of Fyn kinase activity in these events was tested through the use of the protein kinase inhibitor SKI-606 (Bosutinib) and by analysis of Fyn-null oocytes. Suppression of Fyn kinase signaling prior to fertilization caused disruption of the functional polarity of the oocyte with the result that sperm were able to fuse with the oocyte in the immediate vicinity of the meiotic spindle, a region that normally does not allow sperm fusion. The loss of functional polarity was accompanied by disruption of the microvilli and cortical granule-free zone that normally overlie the meiotic spindle. Changes in the distribution of cortical granules and filamentous actin provided further evidence of disorganization of the oocyte cortex. Rho B, a molecular marker for oocyte polarity, was unaffected by suppression of Fyn activity; however, the polarized association of Par-3 with the cortex overlying the meiotic spindle was completely disrupted. The defects in oocyte polarity in Fyn-null oocytes correlated with a failure of the MII chromosomes to maintain a position close to the oocyte cortex which seemed to underlie the above defects in oocyte polarity. This was associated with a delay in completion of meiosis II. Pronuclei, however, eventually formed and subsequent mitotic cleavages and blastocyst formation occurred normally.

摘要

本研究的目的是确定Fyn激酶是否参与精卵相互作用、精子纳入和减数分裂II过程中的信号事件。通过使用蛋白激酶抑制剂SKI-606(博舒替尼)以及对Fyn基因敲除的卵母细胞进行分析,来测试Fyn激酶活性在这些事件中的功能需求。受精前抑制Fyn激酶信号传导会导致卵母细胞功能极性的破坏,结果精子能够在减数分裂纺锤体紧邻区域与卵母细胞融合,而该区域通常不允许精子融合。功能极性的丧失伴随着通常覆盖在减数分裂纺锤体上的微绒毛和无皮质颗粒区的破坏。皮质颗粒和丝状肌动蛋白分布的变化进一步证明了卵母细胞皮质的紊乱。Rho B作为卵母细胞极性的分子标记,不受Fyn活性抑制的影响;然而,Par-3与覆盖减数分裂纺锤体的皮质的极性关联被完全破坏。Fyn基因敲除的卵母细胞中卵母细胞极性的缺陷与MII期染色体未能维持靠近卵母细胞皮质的位置相关,这似乎是上述卵母细胞极性缺陷的基础。这与减数分裂II完成的延迟有关。然而,原核最终形成,随后的有丝分裂分裂和囊胚形成正常发生。

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