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首页> 外文期刊>Scientific reports. >WASH complex regulates Arp2/3 complex for actin-based polar body extrusion in mouse oocytes
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WASH complex regulates Arp2/3 complex for actin-based polar body extrusion in mouse oocytes

机译:WASH复合物调节Arp2 / 3复合物在小鼠卵母细胞中基于肌动蛋白的极体挤压

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摘要

Prior to their fertilization, oocytes undergo asymmetric division, which is regulated by actin filaments. Recently, WASH complex were identified as actin nucleation promoting factors (NPF) that activated Arp2/3 complex. However, the roles of WASH complex remain uncertain, particularly for oocyte polarization and asymmetric division. Here, we examined the functions of two important subunits of a WASH complex, WASH1 and Strumpellin, during mouse oocyte meiosis. Depleting WASH1 or disrupting Strumpellin activity by WASH1 morpholino (MO) injection or Strumpellin antibody injection decreased polar body extrusion and caused oocyte symmetric division, and this may have been due to spindle formation and migration defects. Time lapse microscopy showed that actin filaments distribution and relative amount at the membrane and in the cytoplasm of oocytes was significantly decreased after disrupting WASH complex. In addition, Arp2/3 complex expression was reduced after WASH1 depletion. Thus, our data indicated that WASH complex regulated Arp2/3 complex and were required for cytokinesis and following polar body extrusion during mouse oocyte meiotic maturation.
机译:受精之前,卵母细胞经历不对称分裂,这受肌动蛋白丝的调节。最近,WASH复合物被鉴定为激活Arp2 / 3复合物的肌动蛋白成核促进因子(NPF)。然而,WASH复合物的作用仍然不确定,特别是对于卵母细胞极化和不对称分裂。在这里,我们检查了小鼠卵母细胞减数分裂过程中WASH复合体的两个重要亚基WASH1和Strumpellin的功能。通过注射WASH1吗啉代(MO)或Strumpellin抗体来消耗WASH1或破坏Strumpellin活性会减少极体挤出并引起卵母细胞对称分裂,这可能是由于纺锤体形成和迁移缺陷所致。延时显微镜显示,破坏WASH复合物后,肌动蛋白丝在卵母细胞膜和细胞质中的分布和相对量显着降低。此外,WASH1耗竭后,Arp2 / 3复合物表达降低。因此,我们的数据表明,WASH复合物调节Arp2 / 3复合物,是胞质分裂和小鼠卵母细胞减数分裂成熟过程中极体挤压后所必需的。

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