首页> 外文期刊>The Journal of Reproduction and Development >Hatching and Distribution of Actin Filaments in Mouse Blastocysts Whose Activities of Protein Kinase A were Suppressed by H-89
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Hatching and Distribution of Actin Filaments in Mouse Blastocysts Whose Activities of Protein Kinase A were Suppressed by H-89

机译:H-89抑制蛋白激酶A活性的小鼠胚泡中肌动蛋白丝的孵化和分布

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The role of actin filaments and contractions in hatching was determined in mouse blastocysts whose actin filament bundling abilities had been suppressed by H-89, an inhibitor of protein kinase A. The hatching rate of blastocysts developed from morulae in a medium containing H-89 at a concentration of 4.0 μM was 17.2%, which was significantly lower than the 76.7% of the control blastocysts developed from morulae in a medium without H-89. The rates of blastocysts starting hatching and forming a slit in the zona pellucida were significantly lower in H-89-treated blastocysts (84.4 and 21.9%) than in control blastocysts (100.0 and 90.6%). The lengths of time needed for slit formation in the zona pellucida and for completion of hatching were significantly longer in the H-89-treated blastocysts (27.4 and 43.3 h) than in the control blastocysts (6.5 and 18.8 h). Over the course of 32 h after blastocoel formation, the number of strong contractions was similar in the H-89-treated and control blastocysts, but the number of weak contractions was significantly fewer in the H-89-treated blastocysts (2.41 times) than in the control blastocysts (4.19 times). Although the distribution of actin filaments was similar in the H-89-treated and control blastocysts in the pre-hatching, hatching and post-hatching periods, the rate of H-89-treated blastocysts in which most trophectoderm cells possessed the fluorescence of actin filaments (12.7%) was significantly lower than the 95.0% of the control blastocysts in the pre-hatching period. These results suggest that actin filament-mediated movements of trophectoderm cells contribute to hatching by facilitating the protrusion of trophectoderm cells from a small hole in the zona pellucida and by enlarging the protrusion. We also suggest that the low hatching ability of the treated blastocysts is related to weak contractions with a low frequency and to strong contractions requiring a longer time for re-expansion.
机译:确定了肌动蛋白丝和收缩在孵化中的作用,这是通过蛋白激酶A抑制剂H-89抑制了肌动蛋白丝捆绑能力的小鼠胚泡中的。囊胚的孵化率是由桑ula在含有H-89的培养基中在没有H-89的培养基中,4.0μM的浓度为17.2%,显着低于从桑ula发育的对照胚泡的76.7%。 H-89处理的胚泡(84.4和21.9%)的囊胚开始孵化并在透明带中形成缝隙的比率显着低于对照胚泡(100.0和90.6%)。在H-89处理的胚泡中(27.4和43.3 h),在透明带中形成缝隙和完成孵化所需的时间明显长于对照胚泡(6.5和18.8 h)。在囊胚腔形成后的32小时内,H-89处理和对照囊胚的强收缩次数相近,但H-89处理囊胚的弱收缩数明显少(2.41倍)在对照胚泡中(4.19倍)。尽管在孵化前,孵化和孵化后,肌动蛋白丝在H-89处理和对照胚泡中的分布相似,但是大多数滋养外胚层细胞具有肌动蛋白荧光的H-89处理胚泡的比率在孵化前,长丝(12.7%)显着低于对照胚泡的95.0%。这些结果表明肌动蛋白丝介导的滋养外胚层细胞的运动通过促进滋养外胚层细胞从透明带中的小孔突出并扩大该突出而有助于孵化。我们还建议,处理过的胚泡的孵化能力低与弱收缩,低频收缩和强收缩有关,后者需要更长的时间才能重新扩张。

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